Aspirin, Statins, Non-aspirin NSAIDs, Metformin, and the Risk of Biliary Cancer: A Swedish Population-Based Cohort Study
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Published:2022-01-27
Issue:4
Volume:31
Page:804-810
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ISSN:1055-9965
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Container-title:Cancer Epidemiology, Biomarkers & Prevention
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language:en
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Short-container-title:
Author:
Marcano-Bonilla Lorena12ORCID, Schleck Cathy D.3, Harmsen William S.3, Sadr-Azodi Omid4, Borad Mitesh J.5, Patel Tushar6, Petersen Gloria M.7, Therneau Terry M.3, Roberts Lewis R.8ORCID, Brusselaers Nele9ORCID
Affiliation:
1. 1Clinical and Translational Science, Mayo Clinic Graduate School of Biomedical Sciences, Rochester, Minnesota. 2. 2University of Puerto Rico, School of Medicine, San Juan, Puerto Rico. 3. 3Division of Clinical Trials and Biostatistics, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota. 4. 4Unit of Surgery, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden. 5. 5Division of Hematology/Oncology, Mayo Clinic, Scottsdale, Arizona. 6. 6Department of Transplantation, Mayo Clinic, Jacksonville, Florida. 7. 7Division of Epidemiology, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota. 8. 8Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota. 9. 9Center for Translational Microbiome Research, Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Karolinska Hospital, Stockholm, Sweden.
Abstract
Abstract
Background:
Chemoprevention for biliary tract cancers (BTC), which comprise intrahepatic cholangiocarcinoma (iCCA), extrahepatic cholangiocarcinoma (eCCA), and gallbladder cancer, is controversial. We examined associations between low-dose aspirin, statins, NSAIDs, and metformin with BTC risk.
Methods:
We used a population-based cohort of 5.7 million persons over age 18 without personal history of cancer (except nonmelanoma skin cancer), receiving at least one commonly prescribed drug between July 1, 2005, and December 31, 2012, from the Swedish Prescribed Drug Registry. Hazard ratios (HR) were calculated using age-scaled multivariable-adjusted Cox models.
Results:
2,160 individuals developed BTC. Low-dose aspirin was not associated with BTC risk [HR, 0.93; 95% confidence interval (CI), 0.81–1.07], iCCA (HR, 1.21; 95% CI, 0.93–1.57), eCCA (HR, 0.80; 95% CI, 0.60–1.07), or gallbladder cancer (HR, 0.87; 95% CI, 0.71–1.06). Statins were associated with lower risk of BTC (HR, 0.66; 95% CI, 0.56–0.78), iCCA (HR, 0.69; 95% CI, 0.50–0.95), eCCA (HR 0.54; 95% CI, 0.38–0.76), and gallbladder cancer (HR, 0.72; 95% CI, 0.57–0.91). For all BTC subtypes, combined low-dose aspirin and statins were not associated with lower risk than statins alone. NSAIDs were associated with higher risk of BTC and its subtypes. Metformin was not associated with BTC risk (HR, 0.98; 95% CI, 0.82–1.18), iCCA (HR, 1.06; 95% CI, 0.77–1.48), eCCA (HR, 1.15; 95% CI, 0.82–1.61), or gallbladder cancer (HR, 0.84; 95% CI, 0.63–1.11).
Conclusions:
Statins were associated with a decreased risk of BTC and its subtypes. Low-dose aspirin alone was not associated with a decreased risk, and use of both was not associated with further decrease in risk beyond statins alone.
Impact:
Statins were most consistently associated with a decreased risk of BTC and its subtypes.
Publisher
American Association for Cancer Research (AACR)
Subject
Oncology,Epidemiology
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