Proton Pump Inhibitors Reduce the Risk of Neoplastic Progression in Patients With Barrett's Esophagus

Background & Aims Acid exposure contributes to the development of Barrett's esophagus (BE) and its progression toward esophageal adenocarcinoma. Patients with BE are frequently treated with acid suppressants, but it is unclear whether these prevent the development of BE-related cancer. We i...

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Veröffentlicht in:Clinical gastroenterology and hepatology 2013-04, Vol.11 (4), p.382-388
Hauptverfasser: Kastelein, Florine, Spaander, Manon C.W, Steyerberg, Ewout W, Biermann, Katharina, Valkhoff, Vera E, Kuipers, Ernst J, Bruno, Marco J
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container_end_page 388
container_issue 4
container_start_page 382
container_title Clinical gastroenterology and hepatology
container_volume 11
creator Kastelein, Florine
Spaander, Manon C.W
Steyerberg, Ewout W
Biermann, Katharina
Valkhoff, Vera E
Kuipers, Ernst J
Bruno, Marco J
description Background & Aims Acid exposure contributes to the development of Barrett's esophagus (BE) and its progression toward esophageal adenocarcinoma. Patients with BE are frequently treated with acid suppressants, but it is unclear whether these prevent the development of BE-related cancer. We investigated whether acid suppression reduces the risk of neoplastic progression in patients with BE. Methods We performed a multicenter prospective cohort study of 540 patients with BE. We collected information on medication use at each surveillance visit, which was cross-checked with pharmacy records. Patients also completed a questionnaire about their use of over-the-counter medication. Incident cases of high-grade dysplasia and esophageal adenocarcinoma were identified during a median follow-up period of 5.2 years. Time-dependent Cox regression models were used to investigate the effect of acid suppression on the risk of neoplastic progression. Results Forty patients (7%) developed high-grade dysplasia or esophageal adenocarcinoma during the follow-up period. Use of histamine-2 receptor antagonists did not affect the incidence of neoplastic progression. However, use of proton pump inhibitors (PPIs) at inclusion in the study or during the follow-up period reduced the risk of neoplastic progression (hazard ratio, 0.41; 95% confidence interval, 0.18–0.93 and hazard ratio, 0.21; 95% confidence interval, 0.07–0.66). Prolonged use of PPIs and good adherence were associated with an additional protective effect. The prevalence of esophagitis decreased during PPI use, but length of BE was not affected. Conclusions In a multicenter prospective cohort study, PPI use was associated with a reduced risk of neoplastic progression in patients with BE.
doi_str_mv 10.1016/j.cgh.2012.11.014
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Patients with BE are frequently treated with acid suppressants, but it is unclear whether these prevent the development of BE-related cancer. We investigated whether acid suppression reduces the risk of neoplastic progression in patients with BE. Methods We performed a multicenter prospective cohort study of 540 patients with BE. We collected information on medication use at each surveillance visit, which was cross-checked with pharmacy records. Patients also completed a questionnaire about their use of over-the-counter medication. Incident cases of high-grade dysplasia and esophageal adenocarcinoma were identified during a median follow-up period of 5.2 years. Time-dependent Cox regression models were used to investigate the effect of acid suppression on the risk of neoplastic progression. Results Forty patients (7%) developed high-grade dysplasia or esophageal adenocarcinoma during the follow-up period. Use of histamine-2 receptor antagonists did not affect the incidence of neoplastic progression. However, use of proton pump inhibitors (PPIs) at inclusion in the study or during the follow-up period reduced the risk of neoplastic progression (hazard ratio, 0.41; 95% confidence interval, 0.18–0.93 and hazard ratio, 0.21; 95% confidence interval, 0.07–0.66). Prolonged use of PPIs and good adherence were associated with an additional protective effect. The prevalence of esophagitis decreased during PPI use, but length of BE was not affected. Conclusions In a multicenter prospective cohort study, PPI use was associated with a reduced risk of neoplastic progression in patients with BE.</description><identifier>ISSN: 1542-3565</identifier><identifier>EISSN: 1542-7714</identifier><identifier>DOI: 10.1016/j.cgh.2012.11.014</identifier><identifier>PMID: 23200977</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenocarcinoma - prevention &amp; control ; Aged ; Barrett Esophagus - complications ; Barrett Esophagus - drug therapy ; Cohort Studies ; Esophageal Adenocarcinoma ; Esophageal Neoplasms - prevention &amp; control ; Female ; Gastroenterology and Hepatology ; Gastroesophageal Reflux Disease ; Humans ; Male ; Medication ; Middle Aged ; Prospective Studies ; Proton Pump Inhibitors - therapeutic use ; Risk Factor ; Surveys and Questionnaires</subject><ispartof>Clinical gastroenterology and hepatology, 2013-04, Vol.11 (4), p.382-388</ispartof><rights>AGA Institute</rights><rights>2013 AGA Institute</rights><rights>Copyright © 2013 AGA Institute. Published by Elsevier Inc. 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Patients with BE are frequently treated with acid suppressants, but it is unclear whether these prevent the development of BE-related cancer. We investigated whether acid suppression reduces the risk of neoplastic progression in patients with BE. Methods We performed a multicenter prospective cohort study of 540 patients with BE. We collected information on medication use at each surveillance visit, which was cross-checked with pharmacy records. Patients also completed a questionnaire about their use of over-the-counter medication. Incident cases of high-grade dysplasia and esophageal adenocarcinoma were identified during a median follow-up period of 5.2 years. Time-dependent Cox regression models were used to investigate the effect of acid suppression on the risk of neoplastic progression. Results Forty patients (7%) developed high-grade dysplasia or esophageal adenocarcinoma during the follow-up period. Use of histamine-2 receptor antagonists did not affect the incidence of neoplastic progression. However, use of proton pump inhibitors (PPIs) at inclusion in the study or during the follow-up period reduced the risk of neoplastic progression (hazard ratio, 0.41; 95% confidence interval, 0.18–0.93 and hazard ratio, 0.21; 95% confidence interval, 0.07–0.66). Prolonged use of PPIs and good adherence were associated with an additional protective effect. The prevalence of esophagitis decreased during PPI use, but length of BE was not affected. Conclusions In a multicenter prospective cohort study, PPI use was associated with a reduced risk of neoplastic progression in patients with BE.</description><subject>Adenocarcinoma - prevention &amp; control</subject><subject>Aged</subject><subject>Barrett Esophagus - complications</subject><subject>Barrett Esophagus - drug therapy</subject><subject>Cohort Studies</subject><subject>Esophageal Adenocarcinoma</subject><subject>Esophageal Neoplasms - prevention &amp; control</subject><subject>Female</subject><subject>Gastroenterology and Hepatology</subject><subject>Gastroesophageal Reflux Disease</subject><subject>Humans</subject><subject>Male</subject><subject>Medication</subject><subject>Middle Aged</subject><subject>Prospective Studies</subject><subject>Proton Pump Inhibitors - therapeutic use</subject><subject>Risk Factor</subject><subject>Surveys and Questionnaires</subject><issn>1542-3565</issn><issn>1542-7714</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFu1DAQhiMEoqXwAFyQb3DZ4HHsZCMkJKjaUqmCqoA4Wl57svE2GwePg9S3x9EuHDhw8hz-75fnm6J4CbwEDvXbXWm3fSk4iBKg5CAfFaegpFg1DcjHx7lStTopnhHtOBetbJunxYmoBOdt05wWeBtDCiO7nfcTux57v_EpRGJ36GaLLPXI7jzds9CxzximwVDylmVoG5HIZ9Jn2CSPYyL2w6eefTQxYkqviV1QmHqznel58aQzA-GL43tWfL-8-Hb-aXXz5er6_MPNykoFadUI67BVUAlV18hb5QyXXFm1_NVxXBtQlenM2holneJgRd5QdRtRrx1vN9VZ8ebQO8Xwc0ZKeu_J4jCYEcNMGipoYd1wCTkKh6iNgShip6fo9yY-aOB6sat3OtvVi10NoLPdzLw61s-bPbq_xB-dOfDuEMC85C-PUZPNZiw6H9Em7YL_b_37f2g7-NFbM9zjA9IuzHHM9jRoEprrr8t5l-tCLpGQ1fwGZ0KesQ</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Kastelein, Florine</creator><creator>Spaander, Manon C.W</creator><creator>Steyerberg, Ewout W</creator><creator>Biermann, Katharina</creator><creator>Valkhoff, Vera E</creator><creator>Kuipers, Ernst J</creator><creator>Bruno, Marco J</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20130401</creationdate><title>Proton Pump Inhibitors Reduce the Risk of Neoplastic Progression in Patients With Barrett's Esophagus</title><author>Kastelein, Florine ; 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Aims Acid exposure contributes to the development of Barrett's esophagus (BE) and its progression toward esophageal adenocarcinoma. Patients with BE are frequently treated with acid suppressants, but it is unclear whether these prevent the development of BE-related cancer. We investigated whether acid suppression reduces the risk of neoplastic progression in patients with BE. Methods We performed a multicenter prospective cohort study of 540 patients with BE. We collected information on medication use at each surveillance visit, which was cross-checked with pharmacy records. Patients also completed a questionnaire about their use of over-the-counter medication. Incident cases of high-grade dysplasia and esophageal adenocarcinoma were identified during a median follow-up period of 5.2 years. Time-dependent Cox regression models were used to investigate the effect of acid suppression on the risk of neoplastic progression. Results Forty patients (7%) developed high-grade dysplasia or esophageal adenocarcinoma during the follow-up period. Use of histamine-2 receptor antagonists did not affect the incidence of neoplastic progression. However, use of proton pump inhibitors (PPIs) at inclusion in the study or during the follow-up period reduced the risk of neoplastic progression (hazard ratio, 0.41; 95% confidence interval, 0.18–0.93 and hazard ratio, 0.21; 95% confidence interval, 0.07–0.66). Prolonged use of PPIs and good adherence were associated with an additional protective effect. The prevalence of esophagitis decreased during PPI use, but length of BE was not affected. Conclusions In a multicenter prospective cohort study, PPI use was associated with a reduced risk of neoplastic progression in patients with BE.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23200977</pmid><doi>10.1016/j.cgh.2012.11.014</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Adenocarcinoma - prevention & control
Aged
Barrett Esophagus - complications
Barrett Esophagus - drug therapy
Cohort Studies
Esophageal Adenocarcinoma
Esophageal Neoplasms - prevention & control
Female
Gastroenterology and Hepatology
Gastroesophageal Reflux Disease
Humans
Male
Medication
Middle Aged
Prospective Studies
Proton Pump Inhibitors - therapeutic use
Risk Factor
Surveys and Questionnaires
title Proton Pump Inhibitors Reduce the Risk of Neoplastic Progression in Patients With Barrett's Esophagus
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