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Ulcer, Gastric Surgery and Pancreatic Cancer Risk: an Analysis from the International Pancreatic Cancer Case-Control Consortium (PanC4)

Abstract

Background: Peptic ulcer and its treatments have been associated to pancreatic cancer risk, although the evidence is inconsistent.

Methods: We pooled 10 case-control studies within the Pancreatic Cancer Case-control Consortium (PanC4), including 4717 pancreatic cancer cases and 9374 controls, and estimated summary odds ratios (OR) using multivariable logistic regression models.

Results: The OR for pancreatic cancer was 1.10 [95% confidence interval (CI) 0.98-1.23] for history of ulcer (OR = 1.08 for gastric and 0.97 for duodenal ulcer). The association was stronger for a diagnosis within 2 years before cancer diagnosis (OR = 2.43 for peptic, 1.75 for gastric, and 1.98 for duodenal ulcer). The OR was 1.53 (95% CI 1.15-2.03) for history of gastrectomy; however, the excess risk was limited to a gastrectomy within 2 years before cancer diagnosis (OR = 6.18, 95% CI 1.82-20.96), while no significant increased risk was observed for longer time since gastrectomy. No associations were observed for pharmacological treatments for ulcer, such as antacids, H2-receptor antagonists, or proton-pump inhibitors.

Conclusions: This uniquely large collaborative study does not support the hypothesis that peptic ulcer and its treatment materially affect pancreatic cancer risk. The increased risk for short-term history of ulcer and gastrectomy suggests that any such association is due to increased cancer surveillance.

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References
1.
Moller H, Lindvig K, Klefter R, MOSBECH J, Moller Jensen O . Cancer occurrence in a cohort of patients treated with cimetidine. Gut. 1989; 30(11):1558-62. PMC: 1434324. DOI: 10.1136/gut.30.11.1558. View

2.
Ji B, Chow W, Dai Q, McLaughlin J, Benichou J, Hatch M . Cigarette smoking and alcohol consumption and the risk of pancreatic cancer: a case-control study in Shanghai, China. Cancer Causes Control. 1995; 6(4):369-76. DOI: 10.1007/BF00051413. View

3.
Chan F, Leung W . Peptic-ulcer disease. Lancet. 2002; 360(9337):933-41. DOI: 10.1016/s0140-6736(02)11030-0. View

4.
Smout A, Bogaard J, van Hattum J, Akkermans L . Effects of cimetidine and ranitidine on interdigestive and postprandial lower esophageal sphincter pressures and plasma gastrin levels in normal subjects. Gastroenterology. 1985; 88(2):557-63. DOI: 10.1016/0016-5085(85)90521-9. View

5.
Tascilar M, van Rees B, Sturm P, Tytgat G, Hruban R, Goodman S . Pancreatic cancer after remote peptic ulcer surgery. J Clin Pathol. 2002; 55(5):340-5. PMC: 1769656. DOI: 10.1136/jcp.55.5.340. View