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Screening for esophageal adenocarcinoma and precancerous conditions (dysplasia and Barrett’s esophagus) in patients with chronic gastroesophageal reflux disease with or without other risk factors: two systematic reviews and one overview of reviews to inform a guideline of the Canadian Task Force on Preventive Health Care (CTFPHC)
Systematic Reviews volume 9, Article number: 20 (2020)
Two reviews and an overview were produced for the Canadian Task Force on Preventive Health Care guideline on screening for esophageal adenocarcinoma in patients with chronic gastroesophageal reflux disease (GERD) without alarm symptoms. The goal was to systematically review three key questions (KQs): (1) The effectiveness of screening for these conditions; (2) How adults with chronic GERD weigh the benefits and harms of screening, and what factors contribute to their preferences and decision to undergo screening; and (3) Treatment options for Barrett’s esophagus (BE), dysplasia or stage 1 EAC (overview of reviews).
Bibliographic databases (e.g. Ovid MEDLINE®) were searched for each review in October 2018. We also searched for unpublished literature (e.g. relevant websites). The liberal accelerated approach was used for title and abstract screening. Two reviewers independently screened full-text articles. Data extraction and risk of bias assessments were completed by one reviewer and verified by another reviewer (KQ1 and 2). Quality assessments were completed by two reviewers independently in duplicate (KQ3). Disagreements were resolved through discussion. We used various risk of bias tools suitable for study design. The GRADE framework was used for rating the certainty of the evidence.
Ten studies evaluated the effectiveness of screening. One retrospective study reported no difference in long-term survival (approximately 6 to 12 years) between those who had a prior esophagogastroduodenoscopy and those who had not (adjusted HR 0.93, 95% confidence interval (CI) 0.58–1.50). Though there may be higher odds of a stage 1 diagnosis than a more advanced diagnosis (stage 2–4) if an EGD had been performed in the previous 5 years (OR 2.27, 95% CI 1.00–7.67). Seven studies compared different screening modalities, and showed little difference between modalities. Three studies reported on patients’ unwillingness to be screened (e.g. due to anxiety, fear of gagging). Eleven systematic reviews evaluated treatment modalities, providing some evidence of early treatment effect for some outcomes.
Little evidence exists on the effectiveness of screening and values and preferences to screening. Many treatment modalities have been evaluated, but studies are small. Overall, there is uncertainty in understanding the effectiveness of screening and early treatments.
Systematic review registrations
PROSPERO (CRD42017049993 [KQ1], CRD42017050014 [KQ2], CRD42018084825 [KQ3]).
There are two main types of esophageal cancer. These are, esophageal adenocarcinoma (EAC) where malignant cells form in the tissues of the lower third of the esophagus, primarily in glandular cells where Barrett’s Esophagus (BE) also develops , and esophageal squamous cell carcinoma (ESCC), where malignant cells form in the squamous cells of the esophagus. ESCC is the most prominent form of esophageal neoplasm worldwide, with 398,000 cases of ESCC compared to 52,000 cases of EAC in 2012 . However, EAC is more common than ESCC in Canada and nearly 50% of the worldwide cases of EAC occur in Northwestern Europe and North America . From 1986 to 2006, EAC incidence in Canada rose by 3.9% (1.8 to 3.5 per 100,000) in males and 3.6% (0.2 to 0.5 per 100,000) in females per year . Rates in Canada, provided by the Canadian Cancer Society, report the overall rates of esophageal cancer (combined EAC and ESCC). In 2017, projected new cases of esophageal cancer were 2330 cases (1800 among men and 530 among women) with 2130 deaths from the disease (1650 among men and 480 among women). Although esophageal cancer has a lower incidence than other cancers (ranked 13th among men and 19th among women), it has a high mortality rate and a low 5-year survival rate (14%), the second lowest survival rate after pancreatic cancer . About 20% of EAC cases are diagnosed at an early stage where treatment with surgery leads to a 5-year survival rate of 90% .
Increases in incidence of EAC may be dependent on the increasing prevalence of related risk factors such as obesity and gastroesophageal reflux disease (GERD) . Other risk factors for the development EAC are BE, age 50 years and older, male sex, European descent, current or past smoking, a family history of BE or EAC and a diet low in fruits and vegetables [1, 6,7,8].
The prevalence of GERD in Western countries has increased over the past few decades and is one of the most commonly encountered conditions in primary care practice with an estimated prevalence of between 18–27% in the USA and 9–26% in Europe . Extrapolating these prevalence estimates to the Canadian population, since no Canadian incidence studies exist, would mean that 3.4–6.8 million persons in Canada experience GERD . GERD is a chronic disease with varying definitions [10,11,12,13]. The Montreal definition has been adopted by clinicians and researchers, and defines GERD as “a condition which develops when the reflux of stomach contents causes troublesome symptoms (e.g., retrosternal burning (heartburn), regurgitation) and/or complications (e.g., esophagitis, esophageal stricture)” . According to the American Society for Gastrointestinal Endoscopy, chronic, long-standing GERD is defined as frequent severe GERD symptoms for over 5 years and requiring regular acid suppression therapy . However, experts differ in the definition of the duration of symptoms and whether acid suppression therapy is considered in defining chronic GERD [16,17,18].
The most common complications of GERD are esophagitis, esophageal stricture, BE and EAC . Approximately 60% of people with EAC have experienced symptoms of GERD and there is an association between the frequency and severity of symptoms and increased risk of EAC [19, 20]. In BE, the tissue lining the esophagus transforms into tissue resembling the lining of the intestines. Generally, this transformation is called intestinal metaplasia, and in the esophagus, it is called BE. It is currently not known how the transformation occurs; however, it has been suggested that the acid regurgitation associated with GERD may assist changes at the cellular level . BE is known to develop in around 6–14% of people with GERD, and among those with BE (with or without GERD), 0.2–0.5% develop EAC . However, not all individuals with BE will experience chronic GERD symptoms, and it is still unclear why such a small percentage of people with GERD develop BE [22, 23]. Once an individual is diagnosed with BE, regular surveillance using endoscopy should be considered, as BE can progress over time from low- to high-grade dysplasia and into EAC [24, 25]. Patients who have EAC discovered as a result of endoscopic screening or as part of a surveillance program for BE are diagnosed with earlier-stage tumours, are less likely to have lymph node involvement, and have better short-term life expectancies than those who present with alarm symptoms such as dysphagia and weight loss . It has also been found that the longer the length of BE (e.g. short segment vs. long segment), the higher the risk for EAC .
The goal of treatment for BE and/or low- or high-grade dysplasia is to slow or halt GERD symptoms, reduce mucosal inflammation, control dysplasia and prevent progression to adenocarcinoma . The treatments for EAC depend on the stage of the disorder (0 to 4). For stage 0, the disease is considered precancerous and is synonymous with high-grade dysplasia. Endoscopic therapies (e.g. radiofrequency ablation (RFA) or endoscopic mucosal resection (EMR)) are typically performed, followed by endoscopic surveillance . For stage 1, the disease is generally treated with mechanical methods to remove tissue (e.g. endoscopic mucosal resection) followed by an ablative technique to destroy any remaining abnormal areas in the esophagus lining .
There are four main categories for managing and/or treating the conditions of interest (i.e. stage 1 EAC, BE or dysplasia): (1) pharmacological therapies; (2) surveillance (endoscopic); (3) endoscopic or endoscopic-assisted therapies; and (4) surgery (see Additional file 1). These strategies may overlap with some of the conditions of interest. For example, proton pump inhibitor (PPI) therapy is not a treatment for EAC but may reduce the risk of developing dysplasia and EAC among people with BE. These therapies may also be used in combination (e.g. pharmacological therapy and surveillance procedures for BE) depending on the disease progression.
With Canada’s increasing senior population and longer life expectancy, there is an expected increase in the incidence rates of GERD and EAC, and, therefore, increased demand for gastrointestinal endoscopies [10, 30]. From the Canadian Institute for Health Information National Physician Database, between 2004 and 2008 the number of upper endoscopies performed in Canada has increased by approximately 16% . However, the reason for the endoscopy was not detailed. In order to determine the effectiveness of screening for EAC among GERD patients, the following three key questions (KQs) (Table 1) were addressed through two systematic reviews (SRs) (KQ1 and KQ2) and one overview of reviews (KQ3).
These SRs were developed, conducted and prepared according to the Canadian Task Force for Preventive Health Care (CTFPHC) Procedure Manual  or as methods were updated by the CTPHFC. The protocols for these SRs have been published with PROSPERO (CRD42017049993, CRD42017050014, CRD42018084825) and are available on the CTFPHC website (https://canadiantaskforce.ca/).
These reviews are reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement  (Additional file 2) and includes a PRISMA flow diagram for each key question. We also used AMSTAR (A Measurement Tool to Assess the Methodological Quality of Systematic Reviews) for additional quality control . Any amendments made to the protocols when conducting the reviews have been outlined in Additional file 3.
The analytic framework for these reviews is presented in Fig. 1.
Inclusion and exclusion criteria
Table 2 presents the eligibility criteria for each KQ, using the PICOTS framework.
All search strategies (Additional file 4) were developed and tested through an iterative process by an experienced medical information specialist in consultation with the review teams. In addition, the search strategy for the MEDLINE database was peer-reviewed by another experienced librarian using the Peer Review of Electronic Search Strategies (PRESS) checklist  (Additional file 5). Table 3 presents an overall description of the searching for each KQ.
For each KQ, duplicates across searches were identified and removed using Reference Manager . The remaining articles were uploaded into Distiller Systematic Review (DistillerSR) Software©  for title and abstract screening and full-text screening of the remaining potential relevant articles.
Reviewers performed a pilot testing phase of randomly selected title and abstracts (n = 50) and potentially relevant full-text articles (n = 25) prior to commencing broad screening. Screening forms can be found in Additional file 7. Titles and abstracts were independently screened for relevance by two reviewers, using the liberal accelerated method, which requires one user to include for further assessment at full-text and two reviewers to exclude . References were reviewed in random order, with each reviewer unaware if the reference had already been assessed and excluded by the other reviewer. Subsequently, full-texts were retrieved and two reviewers independently assessed the article for relevancy. Conflicts at full-text were resolved by consensus or a third team member. Articles not available for download were ordered from the library through interlibrary loans. Those that were not received within 30 days were excluded and labelled accordingly. For articles with abstracts only, a search was performed to locate any full-text publications.
Where chronic GERD was not defined in a study (KQ1 and KQ2), we attempted to contact the study authors twice over 2 weeks by email to obtain more information. If authors did not respond, and the lack of definition for chronic GERD was the only reason for possible exclusion, we included the study. Reports in abstract form and protocols were coded as such and excluded, but a search was completed to see if the full-text was available. Those that were not available as full-texts were excluded and studies available only in abstract form are available in the list of excluded studies (Additional file 8).
Data extraction and management
For all KQs, full data extraction was completed by one reviewer using a form developed a priori and 100% of these were verified by a second reviewer (Additional file 9). Any disagreements were resolved by consensus or if needed, with a third reviewer. For KQ1 and KQ2, where information was unclear or missing, authors were contacted by email twice over 2 weeks. If no response was received and the information affected the ability for quantitative analysis, the study was analyzed narratively. For KQ3, data were extracted as they were synthesized and/or reported in the included reviews. No additional information from the primary studies was extracted or assessed and quality control was not performed to verify the accuracy of the reviews’ data on the included studies.
Risk of bias and quality assessment
For KQ1 and KQ2, all included studies were assessed for the risk of bias (RoB) by one reviewer, with verification completed by a second reviewer. The Cochrane RoB tool  was used to evaluate the RoB in RCTs and the Newcastle-Ottawa scale (NOS)  was used to evaluate the RoB in cohort studies. For KQ3, the quality of the included SRs was assessed using the AMSTAR measurement tool . Two reviewers assessed the quality of each included SR independently. Any discrepancies were resolved through discussion and if needed, a third reviewer. We used the AMSTAR 2  approach to determine the final assessments of quality of conduct, including consideration of four critical domains and categorized the quality as high, moderate, low or critically low, using the criteria described in Additional file 10. For all assessments, disagreements were resolved by consensus or third party adjudication.
For all KQs, characteristics of the included studies/reviews are presented in tables and summarised narratively. For KQ1, the results are presented in evidence sets 1 to 8 (Additional file 11), with associated forest plots, where applicable. For KQ2, due to the nature of the data, a meta-analysis of outcomes was not appropriate; however, narrative results are presented. For KQ3, the results presented in evidence sets 1-11 (Additional file 12) may omit some results due to overlap. In the case of overlap where outcome data was the same in multiple reviews, the review with the highest methodological quality or with the most complete outcome data was included; the additional reviews are listed in Additional file 12: Table 1 and mentioned in the Notes column within the evidence sets. For KQ3, odds ratios (OR) were commonly used in SRs and absolute risk differences (ARDs) were calculated accordingly. Where SR authors did not provide an OR, a relative risk (RR) was calculated based on the results and the ARD was calculated based on the RR. In instances where the RR did not approximate the OR reported in the SR, we inserted the RR in the notes column in the evidence set; however, the ARDs were calculated based on the OR. We determined the extent of overlap of evidence across reviews by outcome for each comparison using the corrected covered area (CCA) method .
For KQ1, raw data were extracted from all articles, when available. Raw data were entered into Review Manager Software version 5.3  and hazard ratios (HR) were produced for the survival outcome and risk ratios (RR) were calculated for all other outcomes.
A priori-defined subgroup analysis (KQ1) variables included age, sex, body mass index (BMI), smoking history, duration of chronic GERD, definition of chronic GERD, groupings of risk factors and various ethnic groups. Reporting did not allow for these to be undertaken.
Sensitivity analyses were planned to restrict to those studies as being low risk of bias (KQ1) based on the overall judgement, to address any decisions made regarding handling of data or to explore statistical heterogeneity (KQ1) and based on the timing of publication (KQ1 and KQ2). However, only two studies were considered low risk of bias and therefore sensitivity analysis was not undertaken.
Small study effects
For KQ1 and KQ2, to assess for small study effects, a combination of graphical aids (e.g. funnel plot) and/or statistical tests (e.g. Egger regression test, Hedges-Olkin) were planned if at least ten studies were available in any given analysis. This analysis was not undertaken.
Rating the certainty of the evidence
For each critical and important outcome, the GRADE framework [32, 45] was used to assess the strength and certainty of the evidence. We followed the GRADE guidance for determining the extent of the risk of bias for the body of evidence . The online software GRADEpro GDT (https://gradepro.org/) was used for the GRADE assessments. Assessment of each GRADE domain (study limitations (i.e. risk of bias), indirectness, inconsistency, imprecision and other considerations (i.e. publication bias and comprehensiveness of the search)) was presented, where possible, with the information provided in the studies. If there was missing information, a narrative description was provided. The certainty of the evidence for each outcome, in each study/review, was rated by one reviewer and verified by a second reviewer. Any discrepancies were resolved through consensus.
As KQ3 is an overview, and there are no published methods for performing GRADE for overviews of reviews, we have used the five domains listed above as a guide. As none of the included reviews used GRADE to evaluate the body of evidence, we performed these assessments using the reported information in the reviews and did not access the primary studies for any additional information, as was pre-specified in the protocol. When undertaking domain assessments, we considered an approach with sufficient face validity to align with GRADE guidance. We have elaborated on considerations and decisions in Additional file 13. As with existing GRADE guidance, each GRADE domain was judged as possessing no serious limitations (no rating down), serious limitations (rating down by one) or very serious limitations (rating down by two).
Table 4 provides a summary of the literature search results and Fig. 2a–c shows the PRISMA flow diagrams for each KQ. Study characteristics and population demographics for each key question are presented in Additional file 14 and overall RoB/quality assessment for included studies and reviews are presented in Additional file 15. Additional files 11, 16, 12 provide the evidence set results, narrative results, GRADE evidence profiles and GRADE summary of findings tables for KQ1, KQ2 and KQ3, respectively. The results presented herein provide a high level overview of the results. For additional details of the individual studies and reviews within each section, the full SRs can be found on the CTFPHC website (www.canadiantaskforce.ca). Additional file 8 provides a list of excluded studies at full-text, with reasons for each KQ. A list of ongoing studies for all KQs are provided in Additional file 17.
Key question 1. Effectiveness of screening
Detailed characteristics tables for the ten included studies can be found in Additional 14: Table 1, and results are described herein. The certainty of the evidence to answer KQ1a was very low; therefore, KQ1b was not addressed.
EGD versus no prior EGD
Two retrospective cohort studies by Rubenstein 2008  and Hammad 2019  studied a group of individuals with EAC and evaluated their electronic medical records or the institutional cancer registry to examine if they had a standard sedated esophagogastroduodenoscopy (EGD) in the five years prior to cancer diagnosis or not (Additional file 11: Evidence Set 1). In Rubenstein 2008, survival data, reported using a Kaplan-Meier curve, showed no difference between survival rates at year 1 and 10 . Authors report that there was no difference in long-term survival (approximately 6 to 12 years) between those who had received a prior EGD and those who had not (adjusted HR 0.93, 95% confidence interval (CI) 0.58 to 1.50) [very low certainty]. It was difficult to determine a range of effects across studies for survival analyses as the Hammad 2019 study only had one eligible patient with a prior EGD in the past 5 years.
Both Rubenstein et al.  and Hammad 2019  reported information to evaluate whether an EGD in the previous five years influenced the incidence of EAC by stage of diagnosis at time of detection. It was difficult to determine a range of effects across studies for most stage-based analyses as one study only had one eligible patient with a prior EGD and the stage of diagnosis was unknown (author correspondence) . Rubenstein et al.  reported that there may be a higher odds of a stage 1 diagnosis than a more advanced diagnosis (stages 2–4) (OR 2.77, 95% CI 1.00 to 7.67; p = 0.0497; Forest Plot 1.1) [very low certainty].
EGD versus TNE
Four studies evaluated EGD (sedated) compared to unsedated transnasal esophagoscopy (TNE) (RCTs by Chang 2011  and Sami 2015 ; a randomised crossover study by Jobe 2006 ; one cohort study by Mori 2010 ) (Additional file 11: Evidence Set 2). Sami 2015  evaluated safety, defined as serious adverse events (life-threatening, severe or medical significant consequences of screening), and reported no serious adverse events in either group [very low certainty].
Jobe et al.  reported on incidence of EAC only on those who were receiving initial screening (i.e. excluding those who were being followed with BE). There were no cases of EAC reported [very low certainty]. Three studies [49, 50, 52] defined incidence of endoscopically suspected BE differently. The RCTs showed no significant difference between screening modalities; RR 1.90, 95% CI 0.19 to 19.27  and p = 0.37  [very low certainty]. However, Mori 2010  (cohort study) did show a significant difference, with those being screened with TNE having a higher incidence of suspected BE (RR 2.09, 95% CI 1.30 to 3.36; Forest Plot 2.1) [very low certainty]. Two studies reported no difference in incidence of histologically confirmed BE between screening modalities; p = 0.44  and RR 0.89, 95% CI 0.59 to 1.33  [very low certainty]. Incidence of dysplasia was low, with zero in Chang 2011  and nine (EGD: 5; TNE: 4) in Jobe 2006  showing no difference between screening modalities (RR 1.54, 95% CI 0.44 to 5.44; Forest Plot 2.2) [very low certainty].
Chang 2011 , Sami 2015  and Jobe 2006  used the same measurement tool to measure anxiety (psychological effects); however, there were differences in when the tool was utilized and the reporting of the outcomes were different (e.g. mean, median, level of severity). Therefore, no meta-analysis was performed. There was no difference in anxiety before the procedure (p = 0.084)  [very low certainty], less anxiety overall during the insertion (p = 0.0001)  [very low certainty] and during the procedure (p < 0.001  and p = 0.0001 ) for those who received EGD compared to TNE [very low certainty].
EGD versus video capsule esophagoscopy
One RCT by Chang 2011  evaluated three outcomes, all with very low certainty (Additional file 11: Evidence Set 3). There was no difference in the incidence of endoscopically suspected BE between screening modalities (RR 0.57, 95% CI 0.11 to 3.01; Forest Plot 3.1). Participants with suspected BE based on video capsule esophagoscopy (VCE) (swallowed device) were offered EGD and BE was confirmed through biopsy. Of the three participants with suspected BE who received VCE, none were histologically confirmed cases of BE. There was also no incidence of dysplasia among either group.
EGD versus transoral-EGD
One cohort study by Mori 2010  allowed participants to choose between three screening modalities (sedated EGD, unsedated TNE and unsedated transoral-EGD presented here) (Additional file 11: Evidence Set 4). Overall, there was no difference in the frequency, distribution or severity in the incidence of endoscopically suspected BE between modalities in those with grade 2 or 3 BE (RR 1.30, 95% CI 0.83 to 2.03; Forest Plot 4.1) [very low certainty].
TNE versus VCE
Two studies, Chak 2014  and Chang 2011 , provided data on four outcomes (Additional file 11: Evidence Set 5). There was no difference between screening modalities for incidence of endoscopically suspected BE (RR 0.86, 95% CI 0.29 to 2.56; Forest Plot 5.1) [very low certainty], [49, 53] or for those with histologically confirmed BE (RR 0.62, 95% CI 0.15 to 2.52) [very low certainty] . Chang 2011  reported that there were no incidences of dysplasia with either screening modality [very low certainty].
Those in the unsedated TNE group experienced more anxiety, nervousness or worry (psychological effects) before the procedure than those in the swallowed VCE group (RR 2.28, 95% CI 1.33 to 3.88; Forest Plot 5.2)  [very low certainty], and anxiety during the procedure (RR 2.14, 95% CI 1.22 to 3.77; Forest Plot 5.3)  [very low certainty].
Unsedated TNE versus unsedated transoral EGD
One RCT by Zaman 1999  randomised participants with upper gastrointestinal (GI) symptoms. Mori 2010  (cohort) included those who had previously been screened for upper intestinal tract disorders, and allowed participants to choose between three screening modalities (Additional file 11: Evidence Set 6). Only one complication (life-threatening, severe, or medically significant consequence) was reported (facial swelling followed by surgical exploration and full recovery), with no differences between screening modalities (RR 4.04, 95% CI 0.17 to 95.20; Forest Plot 6.1) [very low certainty] .
Zaman et al.  reported no difference between screening modalities in the incidence of endoscopically suspected BE (three cases total) (RR 0.68, 95% CI 0.07 to 7.09; Forest Plot 6.2) [very low certainty]. Mori et al.  reported a significant difference in the frequency of BE, with those screened with TNE less likely to have suspected BE (grade 2 or 3) compared to transoral EGD (RR 0.62, 95% CI 0.41 to 0.94; Forest Plot 6.3) [very low certainty].
Zaman et al.  evaluated the levels of anxiety before the procedure, during insertion, and during the procedure (psychological effects). Anxiety was assessed on a scale of 10 (higher score representing higher level of anxiety), with no significant difference between levels of anxiety at any time (Forest Plots 6.4-6.6) [very low certainty].
Random biopsy versus enhanced magnification-directed endoscopy biopsies (with acetic acid)
One RCT by Ferguson 2006  included patients who received standard sedated EGD, with those with suspected BE randomised at that point to different biopsy methods (Additional file 11: Evidence Set 7). As all participants were evaluated on suspected BE through EGD, only incidence of histologically confirmed BE is reported. There was no difference in the incidence of histologically confirmed BE between different methods of biopsy. This was found in both those with pattern III and IV specialized intestinal metaplasia (RR 0.98, 95% CI 0.59 to 1.64; Forest Plot 7.1) [very low certainty] and among all specialized intestinal metaplasia pattern types (RR 1.14, 95% CI 0.71 to 1.82; Forest Plot 7.2) [very low certainty].
Random biopsy versus chromoendoscopy
One RCT by Wani 2014  included participants who were given conventional EGD (n = 378) and those with suspected BE who were randomised to either random biopsy (n = 33) or chromoendoscopy (n = 23) (Additional file 11: Evidence Set 8). There was no difference in the number of participants with histologically confirmed BE between methods (RR 0.87; 95% CI 026–2.90; Forest Plot 8.1) [very low certainty].
Key question 2. Patient values and preferences
Three studies (Chak 2014 , Zaman 1999  and Zaman 1998 ) provided information on reasons why participants were unwilling to be part of the study or reasons for deciding against the uptake of screening once allocated . Objectives of the included studies were to determine the acceptance and tolerability of different screening modalities and provide data on screening results. Studies reported on those who refused participation prior to study commencement (i.e. either prior to being screened or prior to randomisation), but did not provide participant characteristics on this patient subset. A narrative summary of the results is provided herein, with detailed results in Additional file 16. No studies provided results on how patients weight the benefits and harms of screening, factors considered in decision to be screened or intrusiveness of the screening modality.
Willingness to be screened
All three studies provided reasons on why those asked had refused to be screened/participate in the study. A large proportion of these individuals were in one study  with 1026 of the 1210 people asked not participating, and 184 who agreed to participate. Among those who did not participate during the invitation period, 627 (52%) did not return the phone call or respond to the letter, 385 (32%) refused to participate (with no reason provided), 12 (1%) were ineligible and two (0.2%) did not participate because of difficulty getting to the hospital. The other two studies by Zaman et al invited 105 outpatients in one study and 62 in the other. Zaman 1999  reported 45 of 105 (43%) patients were unwilling to participate in the study comparing transnasal to peroral EGD. Zaman 1998  reported 19 of 62 (31%) patients unwilling to participate in the study comparing peroral to sedated EGD.
The main reason unwillingness to be screened in both studies was due to anxiety, with 17% (18/105)  and 19% (12/62)  of all those asked to participate reporting this. Both studies also reported that a fear of gagging was the reason, with 10% (10/105)  and 5% (3/62)  reporting this as the reason. Lastly, not being interested in the study (10/105, 10%) , not wishing to undergo a transnasal procedure (7/105, 7%)  and unwillingness to be a study subject (4/62, 6%) were also reported .
Uptake of screening
Chak 2014  reported seven individuals (of 184 randomised) who did not receive the allocated intervention after randomisation. Five people randomised to the TNE group did not receive the procedure because they wanted capsule instead. Two people randomised to the VCE group did not receive the procedure because they were worried about the capsule getting stuck. There was no statistically significant difference in uptake between intervention groups (p = 0.25).
Key question 3. Treatment
The review characteristics of the 11 included SRs are shown in Additional file 14: Table 3. Additional file 12: Table 1 provides additional details of all primary studies included in each SR, and which treatment comparisons provided results in each SR, respectively. Additional file 12: Evidence Sets 1-11 provides detailed results and GRADE tables. Some of the individual trials were represented in more than one review since the reviews did not have mutually exclusive eligibility criteria (Figs. 3 and 4). Twenty-two sets of comparisons had overlapping data across reviews (Additional file 18). In most cases, included studies overlapped completely, according to corrected covered area (CCA) calculations. In few cases, there was discordance among reviews. Throughout the Evidence Sets 1-11, the word “significance” refers to statistical significance unless stated otherwise.
Celecoxib versus placebo
Rees 2010  included one primary RCT  and reported no difference between the groups for all-cause mortality [low certainty] and progression to adenocarcinoma at one year [very low certainty] (three cases per group) (Additional file 12: Evidence Set 1.1). For all-cause mortality, there is discordant reporting within the review, where the text reports two deaths in the trial, but the forest plot reports three deaths in each group. Not presented in the results table but presented narratively in the SR, review authors stated that the primary trial authors did not report any statistical difference for the following outcomes: the area of BE segment at 12 months, and in the reduction in the number of patients progressing from intestinal metaplasia to dysplasia between baseline and 1-year. In addition, review authors reported “no statistical difference in the number of patients” with complete eradication of dysplasia at 12 months, and with bleeding in each group.
Omeprazole versus histamine type 2 receptor antagonists
Rees 2010  reported data from three primary studies [60,61,62], and one was only an abstract . The three studies had differences with regards to drug dosage and regimens (Additional file 14: Table 4). Results and GRADE ratings are presented in Additional file 12: Evidence Set 2.1. There was no difference in the reduction in length (cm) of BE at 12 months between the compared groups, and the pooled effect estimates for both the overall and subgroups (I2 statistic = 62.6% and 60%, respectively) remained non-significant when the analysis was restricted to a subgroup who received a higher dose of omeprazole [very low certainty] [61, 62]. There was a small change in the reduction in area (%) of BE with omeprazole that was statistically significant at 12 months [very low to low certainty] [61, 62].
Photodynamic therapy + omeprazole versus omeprazole alone
Two unique [63, 64] trials (from three studies) [63,64,65] reported across four SRs [58, 66,67,68] reported on patients with BE. Overholt 2007  provided 5-year follow-up data for progression to EAC, with Overholt 2005  providing 2-year follow-up data for other outcomes for the same trial participants (Additional file 12: Evidence Set 3.1). Overholt 2005  and Ackroyd 2000  reported on all-cause mortality, using photodynamic therapy (PDT) with either 5-ALA or porfimer sodium, respectively. Overholt et al. reported no statistically significant difference between groups, but this was based on few observed events (n = 3) and Ackroyd et al. observed no deaths [very low certainty].
At both two- (OR 0.38, 95% CI 0.18 to 0.77)  and five- (RR 0.53, 95% CI 0.31 to 0.91)  years, there was a statistically lower progression to EAC with combined therapy than with omeprazole alone [very low to low certainty]. Progression from non-dysplastic to dysplastic BE was statistically lower with combined therapy (n = 0) compared to the omeprazole group (n = 12) [very low certainty] .
Both reviews show higher eradication of dysplasia with combined therapy [very low to low certainty]; however, there were some data discrepancies between reviews [58, 67] for both studies [64, 65]. Li 2008  provided data among those with HGD from the same studies as the eradication of dysplasia outcome. It is unclear why more participants experienced eradication of HGD than dysplasia in general, as the denominators are the same. There was higher eradication with PDT combined with Omeprazole [very low to low certainty]. Overholt 2007  reported that eradication of BE by 5 years was statistically greater with combined therapy (OR 14.18, 95% CI 5.38 to 37.37) [very low to low certainty].
One study with 36 participants (reported in three reviews) reported on reduction/regression of BE using various measures [58, 67, 68]. Statistically significant reductions in both length and area of BE were observed with combined therapy  in two reviews [very low certainty] [58, 67]. Fayter et al.  provided results of evidence of regression (not further described), with much higher percentage of those in the combined group experiencing regression (89% vs. 11%) [very low certainty].
Statistically significantly more strictures formed with combined therapy (49/138) compared to the omeprazole treatment group (0/70) in one study [very low to low certainty] .
Anti-reflux surgery + Argon plasma coagulation versus anti-reflux surgery + surveillance (endoscopic)
Three systematic reviews [58, 66, 67] reported data from a single trial with two publications [69, 70] on six outcomes (Additional file 12: Evidence Set 4.1). Nissen fundoplication was used for anti-reflux surgery. Ackroyd 2004  was a short-term follow up of the patients, with longer-term follow up presented in Bright 2007 . No patients progressed to cancer [very low certainty] . Based on sparse events (two instances in the surveillance group) in Bright 2007  (in Li 2008 ), no difference between the treatment effects was observed for progression to HGD (from LGD) [very low certainty]. Bright 2007  provided 5-year follow-up data for progression from intestinal metaplasia to dysplasia, and reported no difference between the two groups (two cases of progression in the surveillance group) [very low certainty] [58, 69].
The effect estimate favoured Argon plasma coagulation (APC)  at 12 months for complete eradication of BE [very low certainty]. Note: the data presented in the forest plot differed from the data in the text [58, 69]. No difference was observed between the treatment groups for complete ablation (among those with histological change)  in Li 2008 [very low certainty]. Ackroyd 2004  in De Souza 2014  reported that no difference in treatment failure was observed between the compared groups [very low certainty].
Radiofrequency ablation + proton pump inhibitor versus PPI alone
Three systematic reviews [58, 71, 72] reported data from Shaheen 2009  (Additional file 12: Evidence Set 5.1). Rees et al.  included patients with both low- and high-grade dysplasia; however, Qumseya 2017  and Pandey 2018  restricted their reporting to patients with low-grade dysplasia. Five participants progressed to EAC at 5 years or at the latest timepoint of follow-up (RFA + PPI: 1/84; PPI: 4/43) , resulting in no difference between the compared treatments [low certainty]. Among those with LGD, none progressed to EAC over the follow-up period [low (Rees 2010) and very low certainty (Qumseya 2017)] [58, 71].
Fewer patients progressed to higher grades of dysplasia with the radiofrequency ablation (RFA) treatment [low certainty] . However, there is discrepancy in how this outcome is labelled in the review. The text says there was no data for those progressing from IM to dysplasia and labels it as progression to higher grades of dysplasia, but the forest plot is titled progression from IM to dysplasia. When the outcome was restricted to progression to HGD among patients with LGD, no difference was observed [very low certainty] [71, 72].
There was a statistically significant difference favouring RFA for complete clearance of intestinal metaplasia (RR 17.81, 95% CI 2.61–121.54) [very low certainty] , for complete clearance of dysplasia (OR 22.67, 95% CI 8.72 to 58.94)  [low certainty], which remained when restricted to patients with LGD (OR 0.03, 95% CI 0.01–0.13) [very low certainty] , and for complete eradication of BE (OR 143.53, 95% CI 18.53–1113.87) [low certainty] . De Souza 2014  showed higher rate of treatment failure in the proton pump inhibitor (PPI) treatment group compared to the RFA + PPI group (RFA + PPI: 19/84; PPI: 42/43) [very low certainty].
There was no difference between treatment effects for stricture formatio  [very low certainty]. There were no instances of perforation reported  [very low certainty], and only one study participant developed bleeding, but data was not presented per arm  [very low certainty].
Anti-reflux surgery (Nissen fundoplication) versus H2 receptor agonist/omeprazole
Two systematic reviews [58, 67] reported data from Parrilla 2003  on five outcomes. Overall, the certainty of the evidence was very low for all outcomes (Additional file 12: Evidence Set 6.1). No deaths (all-cause mortality) were reported in either group .
Few participants progressed to EAC, with two in each group (not statistically significant) . Rees 2010  reported a significant difference in the incidence of progression to dysplasia from intestinal metaplasia, with less progression in the surgical treatment group compared with the pharmacological treatment group. Although Li et al.  included the same primary study, the incidence in the surgery group differed from Rees et al., and demonstrated no significant difference between the groups [58, 67]. Because different data were reported for the intervention groups, this led to discordant results between reviews.
Although some participants experienced eradication of dysplasia (surgery: 5/58, H2 receptor antagonist/omeprazole: 3/43) at 5-year follow-up, this was not statistically different between treatment groups . None of the participants experienced complete eradication of BE at 5 years in either treatment group .
PDT with 5-aminolevulinic acid versus PDT with porfimer sodium
MacKenzie 2008  in Rees 2010  reported preliminary data only in abstract form and recruitment had not yet been completed. The certainty of evidence was very low for both outcomes (Additional file 12: Evidence Set 7.1). There was no statistically significant difference in eradication of HGD between the treatment groups (preliminary results included 14 patients in each treatment group) .
These preliminary results showed no difference between treatment groups in stricture formation.
Photodynamic therapy with different treatment parameters
A SR by Fayter 2010  with three primary studies [76,77,78], one of which was an abstract , compared different parameters in the PDT treatment. The certainty of the evidence was very low for cancer risk, and ranged from very low to low for the remaining four outcomes (Additional file 12: Evidence Set 7.2). Generally, higher doses and red light had lower cancer risk and lower rates of adenocarcinoma . These results were considered significant, but were taken from an abstract, so should be interpreted with caution.
Radiofrequency ablation versus surveillance (endoscopic)
Phoa 2014  reported in two systematic reviews [71, 72], included patients with BE with low-grade dysplasia. These reviews also included another primary study by Shaheen et al. ; however, results from this study are presented in Evidence Set 5.1 as another review  states that both treatment groups also received pharmacological therapy (Additional file 12: Evidence Set 8.1). There were seven people with progression to EAC (RFA: 1/68, Surveillance: 6/68) [very low certainty]. Progression per patient-year is also presented [very low certainty]. Qumseya 2017  reported data as cumulative progression from LGD to HGD [very low certainty] and progression per patient-year [very low to low certainty]. Few events were observed (RFA: 0, Surveillance: 12). Pandey 2018  demonstrated a marginally statistically significant results favouring RFA (RR 0.03, 95% CI 0.00 to 0.44) [very low to low certainty] . Although Pandey and Qumseya reported discrepant data for the surveillance group in the number of patients with progression to HGD, 18 and 12, respectively, effect estimates are similar between reviews.
RFA resulted in more patients with complete eradication of dysplasia (RR 3.52, 95% CI 2.40 to 5.17) [very low to low certainty] . A favourable treatment effect was observed with RFA for complete eradication of intestinal metaplasia (RR 123.30, 95% CI 7.78 to 1954.10) [very low to low certainty] .
Eight strictures were formed among the study population; however, data was not reported per arm [very low to low certainty] . None of the study patients developed perforations [very low to low certainty] , and only one study participant developed bleeding, but data was not reported per group [very low to low certainty] .
Argon plasma coagulation + PPI versus multipolar electrocoagulation + PPI
Rees 2010  reported on two primary studies (Additional file 12: Evidence Set 9.1) [80, 81], with no instances of mortality (all-cause) reported [very low to low certainty] and one case of stricture formation in the Argon plasma coagulation (APC) + PPI group [very low certainty].
Multipolar electrocoagulation + PPI versus Argon plasma coagulation + PPI
Two SRs [66, 67] reported the same two primary studies as Evidence Set 9.1; however, the intervention and comparison groups are reversed (Additional file 12: Evidence Set 9.2) [80, 81]. Both outcomes are presented as one review provided the pooled OR (OR 2.01, 95% CI 0.77 to 5.23) [very low certainty] for histological complete ablation of BE  and the other provided the pooled risk difference (RD − 0.14, 95% CI − 0.33 to 0.05) [very low certainty] for treatment failure (the opposite of complete ablation). Both favour multipolar electrocoagulation (MPEC) + PPI .
Photodynamic therapy versus Argon plasma coagulation + PPI
Five systematic reviews [58, 66,67,68, 82] reported on six primary studies [83,84,85,86,87,88] of which some were abstracts (e.g. Zoepf 2003 ) (Additional file 12: Evidence Set 10.1). There were many differences between the SRs and the primary studies within the SRs in how comparison groups were reported, heterogeneity between therapy types (e.g. PDT with 5-ALA or Porfimer sodium), differences in their drug dosing and light delivery regimens  and differences in the participants who were included in the analyses (e.g. all levels of dysplasia or LGD only). Rees 2010  reported on three studies [84,85,86], with a combined incidence of all-cause mortality of one in the PDT group and none in the APC + PPI group [very low certainty] .
Almond 2014  reported on three studies [84, 86, 88] in participants with LDG. One incident case of EAC by 12 months in the PDT group was reported [very low certainty]. Almond et al.  reported no events of progression to high-grade dysplasia among 17 participants [very low certainty] [84, 86].
Rees 2010  and Almond 2014  show discrepant data for the PDT group in Ragunath et al. . The number of patients experiencing complete eradication of dysplasia was reported as 10/13 in Rees 2010, and 8/11 in Almond 2014 [very low certainty]. As Almond et al. included only those with low-grade dysplasia, it might be that the two additional participants in Rees et al. had high-grade dysplasia, although this is not clearly reported. Five SRs [58, 66,67,68, 82] reported on PDT versus APC + PPI and how it affected BE in five primary studies [83,84,85,86,87]. These reviews reported the outcomes in several ways: complete ablation of BE, eradication of BE, reduction of BE (length, surface reduction) and treatment failure (no ablation). Overall, there was a high level of heterogeneity among studies and in the results with very low certainty in all of these outcomes except the reduction in length (cm) which was rated as low certainty. Determining concordance of results across reviews was difficult due to the differences in how information was reported. Almond 2014  reports on Ragunath 2005 , reporting no difference between treatments in eradication of intestinal metaplasia (two participants in each group) [very low certainty].
Both Rees 2010  and Almond 2014  reported on stricture, with Rees 2010 including three primary studies [84,85,86] and Almond 2014 only including Ragunath 2005 . Although there was discordance in the number of those experiencing stricture, neither review reported any difference between treatment groups [very low certainty].
Endoscopic mucosal resection versus radiofrequency ablation
Three SRs [89,90,91] included patients with BE and intramucosal neoplasia (i.e. early stage adenocarcinoma). Although both Fujii-Lau et al.  and Chadwick et al.  include Shaheen 2011  as an included study, because only one of the treatment groups was considered relevant for those reviews, neither reported the results from the placebo group. Therefore, results from Shaheen 2011  are not presented (Additional file 12: Evidence Set 11.1). All three reviews provided results for both treatment groups for the primary study of van Vilsteren 2011 , although all three reviews also label the treatment groups differently (e.g. stepwise EMR vs. focal EMR + RFA, EMR vs. RFA, complete EMR vs. RFA). Both endoscopic mucosal resection (EMR) and radiofrequency ablation (RFA) eradicated neoplasia (eradication of cancer) in most cases (EMR: 100%; RFA: 96%), with no difference between treatments [very low certainty] . Eradication of dysplasia was completed in almost all participants at the end of the treatment and at follow-up. Only one participant in the RFA group did not have complete eradication at the end of treatment and follow-up [very low certainty] . Almost all participants experienced complete eradication of intestinal metaplasia, although there was slight discordance among the percentages reported in the two reviews [very low certainty] [89, 91].
Only one participant in the EMR treatment group experienced recurrence of cancer [very low certainty] , no participant experienced recurrence of dysplasia [low certainty]  and two participants in each treatment group experienced recurrence of intestinal metaplasia [very low certainty] .
Two SRs [89, 91] reported on bleeding, with some data discrepancies, but overall concordant results. One SR  reported that among the 25 participants in the EMR group, only one participant experienced perforations. No one in the RFA group experienced this outcome. Most participants receiving EMR treatment experienced strictures (22 of 25, 88%) compared to only three of 22 (14%) in the RFA group. Review authors did not provide effect estimates, but a risk ratio of 6.45 (95% CI 2.23 to 18.66) for EMR compared to RFA was calculated using these data . Almost all participants receiving EMR experienced stenosis requiring treatment (88%, 22/25), with only three of 21 (14%) experiencing stenosis in the RFA group . This difference was statistically significant with a calculated risk ratio of 6.45 (95% CI 2.23–18.65) for EMR compared with RFA. All of these adverse events were rated as very low certainty.
Esophageal cancer, although lower in incidence relative to other cancers, has a higher mortality rate, partly due to a more advanced stage at diagnosis, when the cancer is widely spread to other vital organs and is incurable. This makes the consideration of whether to invest in screening services important. In 2012, a Cochrane systematic review by Yang et al.  set out to include only RCTs comparing screening versus no screening, and found no studies meeting their inclusion criteria. Five years later, this systematic review found no additional randomised controlled trials comparing screening to no screening. Among the few studies that have assessed the effectiveness of screening of individuals with chronic GERD, there exists several limitations (e.g. small sample sizes, one-time screening test with no follow-up). Although there may be higher odds of stage 1 diagnosis if an EGD had been performed in the previous 5 years, the study included a small number of cases, resulting in low precision . Those diagnosed at earlier stages (T1 and T2) can be treated with potentially curable therapies, for example, esophagectomy in patients with high-grade dysplasia and stage T1a cancer has been associated with a greater survival; 89% at 1 year, 77% at five years and 68% at 10 years . Comparatively, those with late stage cancer that cannot be cured by surgery receive chemotherapy/chemoradiation and have a 15% 5-year survival rate .
There was little difference in the incidence rates of EAC, BE and dysplasia using alternative screening methods. Although EGD with biopsy is considered the gold standard for the diagnosis and surveillance of BE [96, 97], the results from these studies may encourage increased usage of alternative methods of screening for BE and EAC. Conventional EGD uses sedation, which increases the cost of screening (e.g. monitoring patients post-procedure) and resources used (e.g. availability of a gastroenterologist, recovery room). Alternate methods do not require sedation, can be done in a primary care setting and require little monitoring post-procedure. In studies where participants who had experienced a previous screening and were allowed to then select which screening modality they wanted, there was a preference towards unsedated methods. Of the 1574 participants, 721 (46%) chose transnasal, 599 (38%) chose transoral and 254 (16%) chose EGD . Further supporting patient choice of screening modality, RCTs reported higher levels of dropouts and anxiety among those randomised to TNE compared to other screening modalities, although not always significant. The perceived discomfort of the unsedated transnasal procedure could contribute to increased anxiety.
When considering patient values and preferences for screening, the data is also sparse. Three studies reported on the willingness, or in this case the unwillingness, to participate and be screened in a study on screening for EAC and precancerous conditions. One study also provided outcome information on uptake of screening, more specifically reasons why they did not uptake screening after allocation. No other outcomes of interest were addressed in these studies, overall providing little evidence to answer the KQ2. We are not aware of any other reviews that have been done in the area of upper GI screening in relation to how patients weigh the benefits and harms of screening and what factors contribute to these preferences and to their decision to undergo screening, so there is nothing to compare it to.
In our overview evaluating treatment for BE, with or without dysplasia, and early-stage adenocarcinoma (KQ3), 11 SRs were included. Treatment modalities covered pharmacological therapy, various ablative techniques, surgery and some combinations thereof, with a mix of statistically significant and non-significant results, meaning that treatment may show an effect on some outcomes and little to no effect on others. However, there were few studies, all with small sample sizes by outcome, and for many outcomes, only one study provided results, thereby providing little information with which to gauge the certainty of the evidence. In consultation with clinical experts, in addition to evidence from retrospective and prospective clinical series (e.g. AIM trial ), and registry data, certain treatments are currently considered as the standard of care. For example, BE with HGD should be treated with ablation and T1a esophageal cancer (EAC and ESCC) should be treated with endoscopic resection (either endoscopic mucosal resection or endoscopic submucosal resection).
Both reviews and the overview of reviews were developed using rigorous methodological standards, as detailed a priori in registered protocols. There may, however, still be some limitations. There is a risk of missing studies, although we minimized this risk by searching multiple databases and using several techniques to search for grey literature. We included only English and French language studies, and some studies were excluded because we could not get access to the full text (i.e. not available through open access journals or through interlibrary loans). There is a chance that some of these records may have met the inclusion criteria and provided additional results. In KQ3, most records (68%) were excluded during our screening phase due to not meeting the pre-defined SR definition . Reason for exclusion were mainly lack of quality assessment of primary studies and not a study design of interest (either a narrative review or clinical practice guideline based on a non-systematic literature review). Consequently, there is a chance that our conclusions may not be reflective of the totality of relevant, existing evidence. Updating the evidence base is an important research agenda item. Among those that did meet our pre-defined definition, some were excluded because they only included observational studies, or did not separate results of RCTs from observational studies.
When evaluating the results for the effectiveness of screening (KQ1), given the very low certainty of the evidence, true effects may be substantially different or uncertain in light of limitations in the body of evidence. There were several important methodological limitations leading to a moderate or high risk of bias among all study outcomes. The few included studies, and generally small sample sizes leads to imprecise results that could not be assessed for consistency or publication bias. A trend that may continue in this area, as half of the potentially relevant ongoing trials are expecting sample populations of less than 200 participants (Additional file 17). Blinding of participants to screening modality was not possible in these studies. The inability to blind patients could affect psychological outcomes, as a patient might have a preference to one screening modality over another. When evaluating the results for patient values and preferences (KQ2), it was difficult to accurately assess RoB for these studies, as the primary purpose of the included studies was to evaluate acceptability after screening and effectiveness of the screening modality, a different lens to the context of our review. Most outcome data were collected before randomisation, and as there is no formal tool to assess RoB prior to randomisation, these outcomes were not assessed. Measurement bias may be present, as studies did not clearly state how this outcome data were collected. It is not clear how the data were collected among those who refused participation during the consent period, as there is no mention of questionnaires or if and how study personnel collected this information. Only the uptake of screening outcome in one study stated that a non-completion questionnaire was given to ascertain reasons for non-completion. It was difficult to assess the inconsistency among the included studies, mainly due to a lack of information among the studies contributing to outcome results. For example, the largest study invited 1210 participants, with 38% (385/1026) of those declining to participate not providing any information on why they refused. Poor reporting of patient information for those who contributed outcome data was seen in all studies. None reported on the age and sex of these participants, and indication for screening (as described above), making it difficult to understand how comparable these studies might have been. Similarly, the quality of the evidence for treating BE, dysplasia and early-stage cancer (KQ3) was low or very low across the comparisons and outcomes, indicating uncertainty that the observed effects would be representative of the true underlying effect. Poor reporting was a barrier in assessing all domains. Additionally, items within tools such as the Jadad score and Downs & Black do not directly translate to considerations that GRADE guidance suggests for assessing risk of bias. The current limited evidence originated in 11 poorly conducted reviews (two rated as low quality and nine rated as critically low quality), from small RCTs (published between 1996 and 2011 with one published in 2014) with unclear or high risk of bias with short follow-up times. Multicenter trials are needed to increase the power of the evidence base. The lack of a longer patient follow-up time to inform outcomes may be explained by patient retention issues or the cost of following patients long-term.
The lack of a definition of chronic GERD, or even how studies defined GERD, leads to a serious concern for the direct generalizability of the population represented in these studies to the target population of this review. Among studies that did provide a description on how GERD was defined, not all studies used a validated questionnaire to define GERD, while some defined GERD inclusion based on “typical symptoms”. Some studies did not define GERD at all. A standardized definition of chronic GERD would allow trialists to better identify the population of interest. Additionally, as more data accrue, this may lead to more certainty as to whom the evidence would apply (i.e. directness) and with greater precision of the estimate and better quality of conduct (and reporting).
Several outcomes of interest, including mortality, quality of life and overdiagnosis, were not reported in any of the included studies (KQ1). This is mostly because the study results were cross-sectional in nature and these outcomes would require follow-up. In the absence of the outcomes of interest to calculate overdiagnosis, we were unable to address this. The review on patient values and preferences (KQ2) did not provide any results on how patients weight the benefits and harms of screening, factors considered in decision to be screened and intrusiveness of the screening modality. When evaluating treatment options (KQ3), not all outcomes that were considered critical or important were reported. Only one review  reported on mortality, and five of ten reviews with usable data reported on progression to cancer, although at different time periods. Survival, quality of life, psychological effects and overtreatment were not reported in any of the included reviews. Additionally, outcomes that were reported have been reported using several different methods. For example, BE was reported as complete eradication, regression or reduction (e.g. regression in cm, regression in area), making it difficult to combine and compare results across studies. One review  reported the outcome as “treatment failure” which is the opposite of eradication but provides another opportunity for reporting core outcomes across reviews. A quick search by our research team on the Core Outcome Measures in Effectiveness Trials (COMET) web-based repository of core outcome sets (http://www.comet-initiative.org/studies/search) revealed none for BE; the one available for esophageal cancer was in relation to chemotherapy, radiation therapy and surgery, presumably for later-stage cancers. Although we developed our outcomes list a priori with review by various stakeholders, it would be a worthwhile endeavour to formally develop a core outcomes list to inform the conduct of future trials. The outcomes used in this review could be used to start discussions on developing core outcomes in this area. Due to the lack of a core outcome list, the pre-specified protocol missed some of the outcomes that were added post-hoc as we encountered them during screening and assessment of the reviews. Those core outcomes sets can help with consistency of outcome definition and terminology, an issue that was encountered in our reviews for all key questions.
Treatments have also changed over time. For instance, photodynamic therapy is used less frequently, according to clinical expert experience, and there were some treatment options listed in Additional file 1 that were not evaluated (e.g. cryotherapy, endoscopic submucosal resection). This might be because they are newer techniques (not yet included in published SRs) or considered less relevant options to include in a SR. Future SRs may consider conducting network meta-analyses of available treatment options, if there are additional primary studies in this area that have been conducted since the last search date of the included reviews.
Potentially relevant, unpublished trials were identified from our grey literature search and may prove informative for any subsequent updates of these reviews (Additional file 17). The ongoing BEST3 cluster randomised controlled trial in the UK involves 120 primary care practices with a planned sample of 9000 participants. The aims are to assess whether the Cytosponge test for patients with reflux symptoms will be effective in increasing the detection of BE in primary care compared to usual care, and to evaluate cost-effectiveness and patient acceptability. However, only the planned outcomes of the incidence of BE (KQ1), adverse events (KQ1) and patient acceptability (KQ2) may be relevant. Results are anticipated for late 2019.
Implications for research
The current literature contains several methodologic flaws and issues around the certainty of the evidence, which limits our ability in considering the applicability of the evidence. The low quality of reporting in this area is of concern, as it influences the true effects of the interventions, and helps in understanding the similarity across studies and the applicability of the findings in SRs. It underscores the importance of proper, clear and transparent reporting for trials using the CONSORT statement  and for SRs using the PRISMA checklist . Several journals have endorsed and incorporated the CONSORT statement in their instructions to authors. Specialty journals for gastroenterology should consider this approach in order to improve the quality of reporting of RCTs and SRs . We also encourage authors of future SRs to perform GRADE and transparently report information for each domain. This is consistent with recommendations by the REWARD Alliance to reduce research waste and increase its value (http://rewardalliance.net/about/recommendations/), which states that “Investigators, funders, sponsors, regulators, research ethics committees, and journals should systematically develop and adopt standards for the content of study protocols and full study reports, and for data sharing practices”.
A consistent and transparent definition of “chronic GERD” should be developed, which would help update these SRs and guide medical professionals in which patients should be screened for EAC and precancerous lesions. A consistent classification of BE (e.g. Prague Classification) should also be used to allow for comparability between studies.
Most included studies compared one screening method versus another screening method. As EAC is a rare disease, to more accurately assess screening effectiveness, good quality, large multi-centre (including community hospitals and university centres) RCTs on screening versus no screening should be performed. These studies should perform follow-up of the participants over time, with clearly defined pathways, to evaluate EAC-related mortality, survival time and other critical outcomes better reported and defined, as discussed by the Core Outcome Measures in Effectiveness Trials (COMET) initiative .
Overdiagnosis has not been addressed in the current literature. de Gelder 2011  outlines seven approaches to estimating overdiagnosis, depending on choice of numerator and denominator. Individual patient data in studies to test the seven approaches would be ideal. This could provide additional information to a study by Pohl 2005 where it was concluded that overdiagnosis in EAC should be excluded as an explanation for the rise in incidence .
Incorporating a systematic evaluation of patient values and preferences into the evidence considered in developing guidelines is important, and primary studies must contribute to this knowledge base. In addition, considering the gender perspective is important in recruitment strategies, should a screening program ever exist. Researchers can access national initiatives such as the Strategy for Patient-Oriented Research (SPOR) in Canada and the Patient Centered Outcomes Research Institute (PCORI) in the USA, who provide funding in research to integrate patient involvement, which is believed to lead to greater use and uptake of the research results. Additionally, INVOLVE, established in the UK in 1996, supports active public involvement in public and social care research.
The evidence on the effectiveness (benefits and harms) of screening for EAC and precancerous conditions (BE and dysplasia) is sparse and is of very low certainty, making it difficult to conclude whether or not people with chronic GERD should be screened for EAC and precancerous lesions. More and better designed trials are needed and a definition of what is considered chronic GERD should be developed to help identify a patient group where screening can be better targeted to evaluate the effectiveness. Similarly, there is currently insufficient evidence to make firm conclusions on how adults with chronic GERD weigh the benefits and harms of screening, and what factors contribute to these preferences and to their decisions to undergo screening. As the importance of this area is well documented, there is a critical information gap that requires new primary research. Lastly, many treatment modalities for BE have been evaluated in the SR literature, but available evidence is of low or very low quality for most outcomes. Due to several limitations (poorly reported low-quality SRs, unclear or high risk of bias trials with small sample sizes, few studies per treatment modality), there is uncertainty in the effectiveness of these treatments. Large multicentre trials with longer follow-up are needed.
Availability of data and materials
American College of Gastroenterology
American College of Physicians
American Gastroenterological Association
A Measurement Tool to Assess Systematic Reviews
Argon plasma coagulation
Absolute risk difference
Body mass index
Canadian Agency for Drugs and Technologies in Health
Canadian Association of Gastroenterology
Core Outcome Measures in Effectiveness Trials
Canadian Task Force on Preventive Health Care
Enhanced magnification-directed endoscopy
Endoscopic mucosal resection
Esophageal squamous cell carcinoma
Gastroesophageal reflux disease
Grading of Recommendations, Assessment, Development and Evaluation
Population, Interventions, Comparisons, Outcomes, Study design
Proton pump inhibitors
Peer Review of Electronic Search Strategies
Preferred Reporting Items for Systematic Reviews and Meta-Analyses
Randomised controlled trial
Risk of bias
Video capsule esophagoscopy
Domper Arnal MJ, Ferrández Arenas Á, Lanas Arbeloa Á. Esophageal cancer: risk factors, screening and endoscopic treatment in Western and Eastern countries. World J. Gastroenterol. 2015;21:7933–43.
Rubenstein JH, Shaheen NJ. Epidemiology, diagnosis, and management of esophageal adenocarcinoma. Gastroenterology. 2015;149:302–17.
Otterstatter MC, et al. Esophageal cancer in Canada: trends according to morphology and anatomical location. Can J Gastroenterol. 2012;26:723–7.
Canadian Cancer Society’s Advisory Committee on Cancer Statistics; Canadian Cancer Statistics 2017. (2017).
Wani, S. et al. Comparison of endoscopic therapies and surgical resection in patients with early esophageal cancer: a population-based study. Gastrointest. Endosc. 79, 224-232.e1 (2014).
Arnold M, Soerjomataram I, Ferlay J, Forman D. Global incidence of oesophageal cancer by histological subtype in 2012. Gut. 2015;64:381–7.
Kamangar F, Dores GM, Anderson WF. Patterns of cancer incidence, mortality, and prevalence across five continents: defining priorities to reduce cancer disparities in different geographic regions of the world. J Clin Oncol. 2006;24:2137–50.
Shaheen NJ, Falk GW, Iyer PG, Gerson LB. ACG Clinical Guideline: Diagnosis and Management of Barrett’s Esophagus. Am. J. Gastroenterol. 2016;111:30–50.
El-Serag HB, Sweet S, Winchester CC, Dent J. Update on the epidemiology of gastro-oesophageal reflux disease: a systematic review. Gut. 2014;63:871–80.
Fedorak RN, Veldhuyzen van ZS, Bridges R. Canadian Digestive Health Foundation Public Impact Series: gastroesophageal reflux disease in Canada: incidence, prevalence, and direct and indirect economic impact. Can J Gastroenterol. 2010;24:431–4.
Shaheen NJ, et al. Upper endoscopy for gastroesophageal reflux disease: best practice advice from the clinical guidelines committee of the American College of Physicians. Ann. Intern. Med. 2012;157:808–16.
Kahrilas PJ, et al. American Gastroenterological association medical position statement on the management of gastroesophageal reflux disease. Gastroenterology. 2008;135:1383–91.
Jones R, Galmiche JP. Review: what do we mean by GERD?—definition and diagnosis. Aliment Pharmacol Ther. 2005;22:2–10.
Vakil, N. et al. [The Montreal definition and classification of gastroesophageal reflux disease: a global, evidence-based consensus paper]. Z. Gastroenterol. 45, 1125–1140 (2007).
Hirota WK, et al. ASGE guideline: the role of endoscopy in the surveillance of premalignant conditions of the upper GI tract. Gastrointest. Endosc. 2006;63:570–80.
Mahon D, et al. Randomized clinical trial of laparoscopic Nissen fundoplication compared with proton-pump inhibitors for treatment of chronic gastro-oesophageal reflux. Br J Surg. 2005;92:695–9.
Anvari M, et al. A randomized controlled trial of laparoscopic Nissen fundoplication versus proton pump inhibitors for the treatment of patients with chronic gastroesophageal reflux disease (GERD): 3-year outcomes. Surg Endosc. 2011;25:2547–54.
Grant AM, et al. Minimal access surgery compared with medical management for gastro-oesophageal reflux disease: five year follow-up of a randomised controlled trial (REFLUX). BMJ. 2013;346:f1908.
Spechler SJ. Barrett’s esophagus. N. Engl. J. Med. 2014;371:836–45.
Lagergren J, Bergström R, Lindgren A, Nyrén O. Symptomatic gastroesophageal reflux as a risk factor for esophageal adenocarcinoma. N. Engl. J. Med. 1999;340:825–31.
de Jonge PJF, van Blankenstein M, Grady WM, Kuipers EJ. Barrett’s oesophagus: epidemiology, cancer risk and implications for management. Gut. 2014;63:191–202.
Gorospe EC, Wang KK. Barrett oesophagus in 2013: risk stratification and surveillance in Barrett oesophagus. Nat Rev Gastroenterol Hepatol. 2014;11:82–4.
Weijenborg, P. Reflux perception and the esophageal mucosal barrier in gastroesophageal reflux disease. (University of Amsterdam, 2016).
Eloubeidi MA, Provenzale D. Clinical and demographic predictors of Barrett’s esophagus among patients with gastroesophageal reflux disease: a multivariable analysis in veterans. J. Clin. Gastroenterol. 2001;33:306–9.
Lao-Sirieix P, Fitzgerald RC. Screening for oesophageal cancer. Nat Rev Clin Oncol. 2012;9:278–87.
Spechler SJ, Sharma P, Souza RF, Inadomi JM, Shaheen NJ. American gastroenterological association technical review on the management of Barrett’s esophagus. Gastroenterology. 2011;140:e18–52.
Pohl H, et al. Length of Barrett’s oesophagus and cancer risk: implications from a large sample of patients with early oesophageal adenocarcinoma. Gut. 2016;65:196–201.
Alberta Health Services. Management of patients with early esophageal cancer, dysplastic and non-dysplastic Barrett’s esophagus: Clinical Practice Guideline. https://www.albertahealthservices.ca/assets/info/hp/cancer/if-hp-cancer-guide-gi011-barretts-esophagus.pdf (2014).
American Cancer Society. Treating Esophageal cancer by STAGE. https://www.cancer.org/cancer/esophagus-cancer/treating/by-stage.html.
Leddin D, et al. The 2012 SAGE wait times program: survey of access to gastroenterology in Canada. Can J Gastroenterol. 2013;27:83–9.
Armstrong, D. & Khanna, S. Gastrointestinal endoscopy in Canada: national trends from 2004-5 to 2008-9. Can. Journla Gastroenterol. Hepatol. Suppl A, 97A (2012).
Canadian Task for on Preventive Health Care Procedure Manual. (2014).
Moher, D., Liberati, A., Tetzlaff, J. & Altman, D. G. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann. Intern. Med. 151, 264–269, W64 (2009).
Shea BJ, et al. Development of AMSTAR: a measurement tool to assess the methodological quality of systematic reviews. BMC Med Res Methodol. 2007;7:10.
McGowan J, et al. PRESS peer review of electronic search strategies: 2015 Guideline Statement. J. Clin. Epidemiol. 2016;75:40–6.
Reference Manager 12. (Thomson Reuters, 2011).
DistillerSR. (Evidence Partners, 2011).
Khangura S, Konnyu K, Cushman R, Grimshaw J, Moher D. Evidence summaries: the evolution of a rapid review approach. Syst. Rev. 2012;1:10.
Higgins, J. & Green, S. Cochrane handbook for systematic reviews of interventions. (Wiley Online Library, 2008).
Wells, G. et al. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. (2000).
Shea BJ, et al. Development of AMSTAR: a measurement tool to assess the methodological quality of systematic reviews. BMC Med. Res. Methodol. 2007;7:10.
Shea BJ, et al. AMSTAR 2: a critical appraisal tool for systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both. BMJ. 2017;358:j4008.
Pieper D, Antoine S-L, Mathes T, Neugebauer EAM, Eikermann M. Systematic review finds overlapping reviews were not mentioned in every other overview. J. Clin. Epidemiol. 2014;67:368–75.
Review Manager (RevMan). (The Nordic Cochrane Centre, The Cochrane Collaboration, 2014).
Atkins D, et al. Grading quality of evidence and strength of recommendations. BMJ. 2004;328:1490.
Balshem H, et al. GRADE guidelines: 3. Rating the quality of evidence. J Clin Epidemiol. 2011;64:401–6.
Rubenstein JH, Sonnenberg A, Davis J, McMahon L, Inadomi JM. Effect of a prior endoscopy on outcomes of esophageal adenocarcinoma among United States veterans. Gastrointest. Endosc. 2008;68:849–55.
Hammad TA, Thrift AP, El-Serag HB, Husain NS. Missed opportunities for screening and surveillance of Barrett’s esophagus in veterans with esophageal adenocarcinoma. Dig. Dis. Sci. 2019;64:367–72.
Chang JY, et al. Population screening for barrett esophagus: a prospective randomized pilot study. Mayo Clin. Proc. 2011;86:1174–80.
Sami SS, et al. A randomized comparative effectiveness trial of novel endoscopic techniques and approaches for Barrett’s esophagus screening in the community. Am. J. Gastroenterol. 2015;110:148–58.
Jobe BA, et al. Office-based unsedated small-caliber endoscopy is equivalent to conventional sedated endoscopy in screening and surveillance for Barrett’s esophagus: a randomized and blinded comparison. Am. J. Gastroenterol. 2006;101:2693–703.
Mori A, et al. Unsedated transnasal ultrathin esophagogastroduodenoscopy may provide betterdiagnostic performance in gastroesophageal reflux disease. Dis. Esophagus. 2011;24:92–8.
Chak A, et al. Comparative acceptability of transnasal esophagoscopy and esophageal capsule esophagoscopy: a randomized, controlled trial in veterans. Gastrointest. Endosc. 2014;80:774–82.
Zaman A, et al. A randomized trial of peroral versus transnasal unsedated endoscopy using an ultrathin videoendoscope. Gastrointest. Endosc. 1999;49:279–84.
Ferguson DD, et al. Enhanced magnification-directed biopsies do not increase the detection of intestinal metaplasia in patients with GERD. Am. J. Gastroenterol. 2006;101:1611–6.
Wani IR, Showkat HI, Bhargav DK, Samer M. Prevalence and risk factors for Barrett’s esophagus in patients with GERD in Northern India; do methylene blue-directed biopsies improve detection of Barrett’s esophagus compared the conventional method? Middle East J. Dig. Dis. 2014;6:228–36.
Zaman A, Hapke R, Sahagun G, Katon RM. Unsedated peroral endoscopy with a video ultrathin endoscope: patient acceptance, tolerance, and diagnostic accuracy. Am. J. Gastroenterol. 1998;93:1260–3.
Rees, J. R., Lao-Sirieix, P., Wong, A. & Fitzgerald, R. C. Treatment for Barrett’s oesophagus. Cochrane Database Syst. Rev. CD004060 (2010) doi:10.1002/14651858.CD004060.pub2.
Heath EI, et al. Secondary chemoprevention of Barrett’s esophagus with celecoxib: results of a randomized trial. J. Natl. Cancer Inst. 2007;99:545–57.
Caldwell M, Byrne P, Walsh T, Hennessy T. A randomised trial on the effect of acid suppression on regression of Barrett’s oesophagus. Gastroenterology. 1996;110:A74.
Peters FT, et al. Endoscopic regression of Barrett’s oesophagus during omeprazole treatment; a randomised double blind study. Gut. 1999;45:489–94.
Weinstein, W. et al. Omeprazole-induced regression of Barrett’s esophagus: a 2 year, randomized, controlled double blind trial. 110, A294 (1996).
Overholt BF, et al. Five-year efficacy and safety of photodynamic therapy with Photofrin in Barrett’s high-grade dysplasia. Gastrointest. Endosc. 2007;66:460–8.
Ackroyd R, et al. Photodynamic therapy for dysplastic Barrett’s oesophagus: a prospective, double blind, randomised, placebo controlled trial. Gut. 2000;47:612–7.
Overholt BF, et al. Photodynamic therapy with porfimer sodium for ablation of high-grade dysplasia in Barrett’s esophagus: international, partially blinded, randomized phase III trial. Gastrointest. Endosc. 2005;62:488–98.
De Souza TF, et al. Systematic review and meta-analysis of endoscopic ablative treatment of Barrett’s esophagus. Rev. Gastroenterol. Peru Organo Of. Soc. Gastroenterol. Peru. 2014;34:217–24.
Li Y-M, Li L, Yu C-H, Liu Y-S, Xu C-F. A systematic review and meta-analysis of the treatment for Barrett’s esophagus. Dig. Dis. Sci. 2008;53:2837–46.
Fayter D, Corbett M, Heirs M, Fox D, Eastwood A. A systematic review of photodynamic therapy in the treatment of pre-cancerous skin conditions, Barrett’s oesophagus and cancers of the biliary tract, brain, head and neck, lung, oesophagus and skin. Health Technol. Assess. Winch. Engl. 2010;14:1–288.
Bright T, et al. Randomized trial of argon plasma coagulation versus endoscopic surveillance for barrett esophagus after antireflux surgery: late results. Ann. Surg. 2007;246:1016–20.
Ackroyd R, Tam W, Schoeman M, Devitt PG, Watson DI. Prospective randomized controlled trial of argon plasma coagulation ablation vs. endoscopic surveillance of patients with Barrett’s esophagus after antireflux surgery. Gastrointest. Endosc. 2004;59:1–7.
Qumseya BJ, et al. Disease progression in Barrett’s low-grade dysplasia with radiofrequency ablation compared with surveillance: systematic review and meta-analysis. Am. J. Gastroenterol. 2017;112:849–65.
Pandey G, Mulla M, Lewis WG, Foliaki A, Chan DSY. Systematic review and meta-analysis of the effectiveness of radiofrequency ablation in low grade dysplastic Barrett’s esophagus. Endoscopy. 2018;50:953–60.
Shaheen NJ, et al. Radiofrequency ablation in Barrett’s esophagus with dysplasia. N. Engl. J. Med. 2009;360:2277–88.
Parrilla P, et al. Long-term results of a randomized prospective study comparing medical and surgical treatment of Barrett’s esophagus. Ann. Surg. 2003;237:291–8.
Mackenzie G, et al. Preliminary results of a randomised controlled trial into the safety and efficacy of ala versus photofrin photodynamic therapy for high grade dysplasia in Barrett’s oesophagus. Gut. 2008;57:A14.
Mackenzie G, et al. Low incidence of esophageal adenocarcinoma following optimal regimen of ALA PDT for High Grade Dysplasia in Barrett’s Esophagus. Gastrointest. Endosc. 2007;65:AB132.
Mackenzie GD, et al. Optimal conditions for successful ablation of high-grade dysplasia in Barrett’s oesophagus using aminolaevulinic acid photodynamic therapy. Lasers Med. Sci. 2009;24:729–34.
Kelty CJ, Ackroyd R, Brown NJ, Brown SB, Reed MWR. Comparison of high- vs low-dose 5-aminolevulinic acid for photodynamic therapy of Barrett’s esophagus. Surg. Endosc. 2004;18:452–8.
Phoa KN, et al. Radiofrequency ablation vs endoscopic surveillance for patients with Barrett esophagus and low-grade dysplasia: a randomized clinical trial. JAMA. 2014;311:1209–17.
Dulai GS, Jensen DM, Cortina G, Fontana L, Ippoliti A. Randomized trial of argon plasma coagulation vs. multipolar electrocoagulation for ablation of Barrett’s esophagus. Gastrointest. Endosc. 2005;61:232–40.
Sharma P, et al. A randomised controlled trial of ablation of Barrett’s oesophagus with multipolar electrocoagulation versus argon plasma coagulation in combination with acid suppression: long term results. Gut. 2006;55:1233–9.
Almond LM, Hodson J, Barr H. Meta-analysis of endoscopic therapy for low-grade dysplasia in Barrett’s oesophagus. Br. J. Surg. 2014;101:1187–95.
Hage M, et al. Molecular evaluation of ablative therapy of Barrett’s oesophagus. J. Pathol. 2005;205:57–64.
Hage M, et al. 5-aminolevulinic acid photodynamic therapy versus argon plasma coagulation for ablation of Barrett’s oesophagus: a randomised trial. Gut. 2004;53:785–90.
Kelty CJ, et al. Endoscopic ablation of Barrett’s oesophagus: a randomized-controlled trial of photodynamic therapy vs. argon plasma coagulation. Aliment. Pharmacol. Ther. 2004;20:1289–96.
Ragunath K, et al. Endoscopic ablation of dysplastic Barrett’s oesophagus comparing argon plasma coagulation and photodynamic therapy: a randomized prospective trial assessing efficacy and cost-effectiveness. Scand. J. Gastroenterol. 2005;40:750–8.
Zoepf, T. et al. Photodynamic therapy (PDT) versus argon plasma, coagulation (APC) for ablative therapy of Barrett’s esophagus. in vol. 57 AB139 (Gastrointest Endosc, 2003).
Zöpf, T. et al. [Photodynamic therapy of dysplasias and early carcinomas in Barrett esophagus with a diode laser system—a pilot study]. Med. Klin. Munich Ger. 1983 96, 212–216 (2001).
Chadwick, G. et al. Systematic review comparing radiofrequency ablation and complete endoscopic resection in treating dysplastic Barrett’s esophagus: a critical assessment of histologic outcomes and adverse events. Gastrointest. Endosc. 79, 718-731.e3 (2014).
Fujii-Lau LL, et al. Recurrence of intestinal metaplasia and early neoplasia after endoscopic eradication therapy for Barrett’s esophagus: a systematic review and meta-analysis. Endosc. Int. Open. 2017;5:E430–49.
Desai, M. et al. Efficacy and safety outcomes of multimodal endoscopic eradication therapy in Barrett’s esophagus-related neoplasia: a systematic review and pooled analysis. Gastrointest. Endosc. 85, 482-495.e4 (2017).
Shaheen NJ, et al. Durability of radiofrequency ablation in Barrett’s esophagus with dysplasia. Gastroenterology. 2011;141:460–8.
van Vilsteren FGI, et al. Stepwise radical endoscopic resection versus radiofrequency ablation for Barrett’s oesophagus with high-grade dysplasia or early cancer: a multicentre randomised trial. Gut. 2011;60:765–73.
Yang S, et al. Screening for oesophageal cancer. Cochrane Database Syst Rev. 2012;12:CD007883.
Rice TW, et al. Superficial adenocarcinoma of the esophagus. J Thorac Cardiovasc Surg. 2001;122:1077–90.
Sanghi V, Thota PN. Barrett’s esophagus: novel strategies for screening and surveillance. Ther. Adv. Chronic Dis. 2019;10.
Lim YC, Fitzgerald RC. Diagnosis and treatment of Barrett’s oesophagus. Br. Med. Bull. 2013;107:117–32.
Robinson KA, et al. Integration of existing systematic reviews into new reviews: identification of guidance needs. Syst. Rev. 2014;3:60.
Schulz KF, Altman DG, Moher D. CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials. BMJ. 2010;340:c332.
Moher D, et al. Does quality of reports of randomised trials affect estimates of intervention efficacy reported in meta-analyses? Lancet. 1998;352:609–13.
Clarke M. Standardising outcomes for clinical trials and systematic reviews. Trials. 2007;8:39.
de Gelder R, et al. Interpreting overdiagnosis estimates in population-based mammography screening. Epidemiol Rev. 2011;33:111–21.
Pohl H, Welch HG. The role of overdiagnosis and reclassification in the marked increase of esophageal adenocarcinoma incidence. J. Natl. Cancer Inst. 2005;97:142–6.
We would like to acknowledge the contribution of the following individuals: Raymond Daniel for reference acquisition and management for the projects. Doreen Whelan for screening of titles and abstract and full-text articles for KQ1 and Vesa Basha for screening full-text articles for KQ1. The Public Health Agency of Canada Global Health and Guidelines Division: Marion Doull (Conceptualization [KQ1, KQ2, KQ3], Writing—review & editing [KQ1, KQ2]), Alejandra Jaramillo-Garcia (Writing—review & editing [KQ1, KQ2]), Heather Limburg (Conceptualization [KQ3], Writing—review & editing [KQ1, KQ2, KQ3]), Mark Avey (Writing—review & editing [KQ3]), Susan Courage (Writing—review & editing [KQ3]), Bradley Mitchelmore (Writing—review & editing [KQ3]), Rachel Rodin (Conceptualization [KQ1, KQ2, KQ3], Writing—review & editing [KQ1, KQ2, KQ3]). Members of the Esophageal Adenocarcinoma Working Group: Stéphane Groulx [chair], Scott Klarenbach, Harminder Singh, Brett D. Thombs, and Brenda Wilson (Conceptualization (KQ1, KQ2, KQ3), Writing—review & editing (KQ1, KQ2, KQ3))
External Working Group clinical experts: Laura Targownik and Paul James Belletrutti (Conceptualization (KQ1, KQ2, KQ3), Writing—review & editing (KQ1, KQ2, KQ3)). Canadian Task Force on Preventive Health Care members not part of the Esophageal Adenocarcinoma Working Group: Heather Colquhoun (Writing—review & editing [KQ1, KQ2, KQ3]), Roland Grad (Writing—review & editing [KQ1, KQ2]), Eddy Lang (Writing—review & editing [KQ1, KQ2]), John C. LeBlanc (Writing—review & editing [KQ1, KQ2, KQ3]), Gabriela A. Lewin (Writing—review & editing [KQ1, KQ2]), Ainsley Moore, (Writing—review & editing [KQ3]), Nav Persaud (Writing—review & editing [KQ3]), Donna L. Reynolds (Writing—review & editing [KQ1, KQ2, KQ3]), John J. Riva (Writing—review & editing [KQ3]), Guylene Theriault (Writing—review & editing [KQ1, KQ2, KQ3]), Cello Tonelli (Writing—review & editing [KQ1, KQ2]). Stakeholders: Ed Kucharski (Writing—review & editing [KQ1, KQ2]), Bruce Greenwald (Writing—review & editing [KQ1, KQ2]), Carole Mayer (Writing—review & editing [KQ1, KQ2, KQ3]), Marjorie Morrison (Writing—review & editing [KQ1, KQ2, KQ3]), Shawn Chirrey (Writing—review & editing [KQ1, KQ2, KQ3]), Christopher Teshima (Writing—review & editing [KQ1, KQ2, KQ3]), Arthur Zalev (Writing—review & editing [KQ1, KQ2, KQ3]), Grigorios Leontiadis (Writing—review & editing [KQ3]), Gilles Plourde (Writing—review & editing [KQ1, KQ2, KQ3]), Huiming Yang (Writing—review & editing [KQ1, KQ2]). External reviewer: Edoardo Savarino (Writing—review & editing [KQ1, KQ2]). Detailed descriptions of Task Force members are available at https://canadiantaskforce.ca.
CH: Conceptualization (KQ1, KQ2, KQ3), data curation (KQ1, KQ2, KQ3), formal analysis (KQ1, KQ2, KQ3), investigation (KQ1, KQ2, KQ3), methodology (KQ1, KQ2, KQ3), project administration (KQ1, KQ2), supervision (KQ1, KQ2, KQ3), validation (KQ1, KQ2, KQ3), visualization (KQ1, KQ2, KQ3), writing—original draft (KQ1, KQ2, KQ3), writing—review and editing (KQ1, KQ2, KQ3). NA: data curation (KQ3), formal analysis (KQ3), investigation (KQ3), methodology (KQ3), project administration (KQ3), supervision (KQ3), validation (KQ3), visualization (KQ3), writing—original draft (KQ3), writing—review and editing (KQ3). AB: conceptualization (KQ1, KQ2, KQ3), data curation (KQ1, KQ2, KQ3), formal analysis (KQ1, KQ2), investigation (KQ1, KQ2, KQ3), project administration (KQ1, KQ2, KQ3), validation (KQ1, KQ2), writing—original draft (KQ3), writing—review and editing (KQ1, KQ2, KQ3). MT: data curation (KQ1, KQ3), investigation (KQ1, KQ3), validation (KQ1, KQ3), writing—review & editing (KQ1, KQ3). BS: methodology (KQ1, KQ2, KQ3), writing—review and editing (KQ1, KQ2, KQ3). KP: data curation (KQ3), investigation (KQ3), validation (KQ3), writing—review and editing (KQ3). LB: writing—review and editing (KQ2). AC: conceptualization (KQ3), writing—review and editing (KQ1, KQ3). KD: writing—review and editing (KQ2). LF: conceptualization (KQ3), writing—review and editing (KQ3). DEM: conceptualization (KQ3), writing—review and editing (KQ1, KQ2, KQ3). BJS: methodology (KQ1, KQ2, KQ3), writing—review and editing (KQ1, KQ2, KQ3). BH: methodology (KQ1, KQ2, KQ3), resources (KQ1, KQ2, KQ3), supervision (KQ1, KQ2, KQ3), writing—review and editing (KQ1, KQ2, KQ3). JL: funding acquisition (KQ1, KQ2, KQ3), methodology (KQ1, KQ2, KQ3), supervision (KQ1, KQ2, KQ3), writing—review and editing (KQ1, KQ2, KQ3). DM: funding acquisition (KQ1, KQ2, KQ3), methodology (KQ1, KQ2), supervision (KQ1, KQ2), writing—review and editing (KQ1, KQ2). AS: conceptualization (KQ1, KQ2, KQ3), data curation (KQ3), formal analysis (KQ3), investigation (KQ3), methodology (KQ1, KQ2, KQ3), project administration (KQ1, KQ2, KQ3), supervision (KQ1, KQ2, KQ3), validation (KQ3), visualization (KQ3), writing—original draft (KQ3), writing—review and editing (KQ1, KQ2, KQ3).
Funding for the systematic reviews and overview of reviews was provided by the Public Health Agency of Canada, with funds distributed by the Nova Scotia Health Research Foundation. This funding supported the development of the protocol, execution of search strategies, collection of the data, data management, analyses and writing of the technical reports. Staff at the Global Health and Guidelines Division at the Public Health Agency of Canada reviewed and provided feedback on the protocol and draft technical reports, but was not involved in the study selection, data extraction, or analysis.
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DM is Co-Editor-in-Chief with Systematic Reviews. BH has previously received honoraria from Cornerstone Research Group for the provision of methodologic advice related to systematic reviews and meta-analysis.
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Hamel, C., Ahmadzai, N., Beck, A. et al. Screening for esophageal adenocarcinoma and precancerous conditions (dysplasia and Barrett’s esophagus) in patients with chronic gastroesophageal reflux disease with or without other risk factors: two systematic reviews and one overview of reviews to inform a guideline of the Canadian Task Force on Preventive Health Care (CTFPHC). Syst Rev 9, 20 (2020). https://doi.org/10.1186/s13643-020-1275-2
- Esophageal adenocarcinoma
- Gastroesophageal reflux disease
- Barrett’s esophagus
- Patient values and preferences
- Systematic review
- Overview of reviews