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Risk of gastric cancer, gastrointestinal cancers and other cancers: a comparison of treatment with pantoprazole and other proton pump inhibitors
Author(s) -
Schneider J. L.,
Kolitsopoulos F.,
Corley D. A.
Publication year - 2016
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/apt.13450
Subject(s) - pantoprazole , medicine , gastroenterology , cancer , hazard ratio , proton pump inhibitor , confounding , proportional hazards model , cumulative incidence , helicobacter pylori , cohort , omeprazole , confidence interval
Summary Background Proton pump inhibitors ( PPI s) have been shown to be carcinogenic in rodent studies. Aim As part of a long‐term post‐marketing surveillance study requested by the US Food and Drug Administration, to compare incidence rates of gastric and other cancers after sustained exposures to pantoprazole, a long‐acting PPI , compared with other shorter acting PPI s. Methods We conducted a cohort study within the membership of the Kaiser Permanente Northern California healthcare system and compared rates of gastric and other cancers among pantoprazole users and users of other PPI medications. The Cox proportional hazards model was used to adjust for potential confounders such as sex, age, receipt of treatment for Helicobacter pylori, cumulative PPI dose, total years PPI treatment and year of index date. The study was developed in consultation with, and approved by, the FDA . Results A total of 61 684 persons with at least a 240‐day supply of medication (34 178 pantoprazole and 27 686 other PPI s) were followed up for a total of 547 020 person‐years (274 700 vs. 272 321 person‐years, respectively). The primary analyses demonstrated comparable risks between the pantoprazole and other PPI groups for gastric cancer [hazard ratio ( HR ) = 0.68, 95% CI 0.24–1.93); colorectal, liver, pancreatic, or small bowel cancers ( HR = 0.95, 95% CI 0.65–1.40) or any cancer ( HR = 1.06, 95% CI 0.93–1.21). Conclusions We found no evidence that pantoprazole, a longer acting PPI , compared with shorter‐acting agents, conferred an excess risk of gastric cancer, other gastrointestinal cancers or all cancers for pantoprazole compared with other shorter‐acting PPI s.