4.6 Article

Comparative Effect of Initiating Metformin Versus Sulfonylureas on Breast Cancer Risk in Older Women

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EPIDEMIOLOGY
卷 28, 期 3, 页码 446-454

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/EDE.0000000000000635

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资金

  1. Pharmacoepidemiology Gillings Innovation Lab (PEGIL) for the Population-Based Evaluation of Drug Benefits and Harms in Older US Adults [GIL 200811.0010]
  2. Center for Pharmacoepidemiology, Department of Epidemiology, UNC Gillings School of Global Public Health
  3. CER Strategic Initiative of UNC's Clinical Translational Science Award [UL1TR001111]
  4. Cecil G. Sheps Center for Health Services Research, UNC
  5. UNC School of Medicine
  6. National Institute on Aging (NIA) [R01 AG023178]
  7. National Institutes of Health (NIH) [R01 CA174453, R01 HL118255, R21-HD080214]
  8. Comparative Effectiveness Research (CER) Strategic Initiative
  9. NC TraCS Institute
  10. UNC Clinical and Translational Science Award [UL1TR001111]
  11. Center for Pharmacoepidemiology
  12. Amgen
  13. AstraZeneca
  14. National Institutes of Health (NIH), National Heart Lung and Blood Institute (NHLBI) [R01 HL118255]
  15. NIH National Institute on Aging (NIA) [R01 AG023178]
  16. NIH National Center for Advancing Translational Sciences (NCATS) [1UL1TR001111]
  17. Center for Pharmacoepidemiology in the Department of Epidemiology, Gillings School of Global Public Health
  18. NIH/NCI [R01CA155342, R21CA175983, P01CA154292, HHSN261201100031C, R01CA149365]
  19. UNC Oncology Clinical Translational Research Training Program [5K12CA120780]
  20. Principal Investigator of a Research Starter Award from the Pharmaceutical Research and Manufacturers of America (PhRMA) Foundation

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Background: Several observational studies have reported that metformin may be associated with reduced risk of breast cancer; however, many of these studies were affected by time-related biases such as immortal time bias and time-window bias. This study aimed to examine the relative risk of breast cancer for older women initiating metformin versus sulfonylureas while avoiding such biases. Methods: The study cohort consisted of women aged 65 vertical bar who initiated monotherapy with metformin (n = 45,900) or sulfonylureas (n = 13,904) and were free of cancer and renal disease within 6 months before treatment initiation using 2007-2012 US Medicare claims data. We followed treatment initiators for incident breast cancer, and estimated hazard ratios using weighted Cox models. Unmeasured confounding by body mass index and smoking was further adjusted by propensity score calibration using external information from Medicare Current Beneficiary Survey 2006-2009 panels. Results: During 58,835 and 16,366 person-years of follow-up, 385 initiators of metformin treatment and 95 of sulfonylurea were diagnosed with breast cancer. Metformin initiators did not have a reduced risk of breast cancer compared with sulfonylurea initiators (hazard ratio: 1.2; 95% confidence interval: 0.94, 1.6). Externally controlling for body mass index and smoking did not affect the estimates. Conclusion: The findings of this study provide no support for a reduced risk of breast cancer after initiation of metformin compared with a clinical alternative in older women. This study is limited by the relatively short follow-up time and we cannot exclude the possible benefits of long-time metformin use on breast cancer risk.

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