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  4. Sitagliptin May Reduce Breast Cancer Risk in Women With Type 2 Diabetes
 
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Sitagliptin May Reduce Breast Cancer Risk in Women With Type 2 Diabetes

Journal
Clinical Breast Cancer
Journal Volume
17
Journal Issue
3
Pages
211-218
Date Issued
2017
Author(s)
CHIN-HSIAO TSENG  
DOI
10.1016/j.clbc.2016.11.002
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85008220555&doi=10.1016%2fj.clbc.2016.11.002&partnerID=40&md5=1f61642861284850bcb6271fa09cef8f
https://scholars.lib.ntu.edu.tw/handle/123456789/496060
Abstract
Breast cancer risk associated with sitagliptin use was evaluated in female patients with diabetes. The overall hazard ratio was 0.718 (95% confidence interval, 0.573-0.901). When evaluated by the tertiles of cumulative duration and cumulative dose, a significant risk reduction was noted in the third tertiles (ie, > 12.73 months and > 33,800 mg, respectively). The findings supported a reduced risk after prolonged use of sitagliptin. Background Whether sitagliptin may affect breast cancer risk remains to be answered. This study evaluated such an association in Taiwanese female patients with type 2 diabetes. Methods A retrospective cohort of female patients with newly diagnosed type 2 diabetes at an age ≥ 25 years between 1999 and 2010 was recruited from the National Health Insurance database. A total of 32,457 ever-users and 396,021 never-users of sitagliptin were followed until December 31, 2011. The treatment effect was estimated by Cox regression incorporated with the inverse probability of treatment weighting using propensity score. Sensitivity analyses were conducted in a matched cohort. Results During follow-up, 78 ever-users and 2204 never-users were diagnosed with breast cancer, representing an incidence of 150.44 and 215.87 per 100,000 person-years, respectively. The hazard ratio (95% confidence intervals [CIs]) for ever- versus never-users was 0.718 (95% CI, 0.573-0.901). The hazard ratio for the first, second, and third tertile of cumulative duration < 5.73, 5.73-12.73, and > 12.73 months was 0.783 (95% CI, 0.523-1.171), 1.021 (95% CI, 0.723-1.441), and 0.455 (95% CI, 0.296-0.700), respectively; and was 0.823 (95% CI, 0.554-1.222), 0.918 (95% CI, 0.639-1.317), and 0.499 (95% CI, 0.331-0.753) for cumulative dose < 14,400, 14,400-33,800, and > 33,800 mg, respectively. Findings were supported by analyses in the matched cohort. Conclusions Sitagliptin may reduce breast cancer risk in female patients with type 2 diabetes mellitus, especially 1 year after its use. ? 2016 Elsevier Inc.
Subjects
Incretin; National Health Insurance; Population-based study; Propensity score; Taiwan
SDGs

[SDGs]SDG3

Other Subjects
exendin 4; metformin; pioglitazone; rosiglitazone; saxagliptin; sitagliptin; sulfonylurea; vildagliptin; antidiabetic agent; sitagliptin; adult; age; Article; breast cancer; cancer risk; cohort analysis; drug effect; drug use; female; follow up; human; major clinical study; non insulin dependent diabetes mellitus; retrospective study; risk reduction; Taiwanese; breast tumor; incidence; middle aged; non insulin dependent diabetes mellitus; prognosis; risk factor; Taiwan; Adult; Breast Neoplasms; Diabetes Mellitus, Type 2; Female; Follow-Up Studies; Humans; Hypoglycemic Agents; Incidence; Middle Aged; Prognosis; Retrospective Studies; Risk Factors; Sitagliptin Phosphate; Taiwan
Publisher
Elsevier Inc.
Type
journal article

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