Tamoxifen use and acute pancreatitis: A population-based cohort study

被引:0
|
作者
Hsu, Fan-Gen [1 ,2 ]
Hsieh, Yow-Wen [1 ,2 ]
Sheu, Ming-Jyh [1 ]
Lin, Che-Chen [3 ,4 ]
Lin, Cheng-Li [4 ]
Hsu, Chung Y. [5 ]
Lee, Chang-Yin [6 ,7 ]
Chang, Mei-Yin [8 ]
Chang, Kuang-Hsi [9 ]
机构
[1] China Med Univ, Sch Pharm, Taichung, Taiwan
[2] China Med Univ Hosp, Dept Pharm, Taichung, Taiwan
[3] Taichung Vet Gen Hosp, Healthcare Serv Res Ctr, Taichung, Taiwan
[4] China Med Univ Hosp, Management Off Hlth Data, Taichung, Taiwan
[5] China Med Univ, Grad Inst Clin Med Sci, Taichung, Taiwan
[6] I Shou Univ, Sch Chinese Med Post Baccalaureate, Coll Med, Yancho Campus, Kaohsiung, Taiwan
[7] E DA Hosp, Dept Chinese Med, Kaohsiung, Taiwan
[8] Fooyin Univ, Sch Med & Hlth Sci, Dept Med Lab Sci & Biotechnol, Kaohsiung, Taiwan
[9] China Med Univ, Inst Biomed Sci, Taichung, Taiwan
来源
PLOS ONE | 2017年 / 12卷 / 03期
关键词
INDUCED HYPERTRIGLYCERIDEMIA; BREAST-CANCER; PHASE-II; RISK; DRUGS;
D O I
10.1371/journal.pone.0173089
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Several case reports have indicated that tamoxifen induced acute pancreatitis (AP); but no pharmacoepidemiological data support the claim. Therefore, we investigated whether tamoxifen use is correlated with the risk of AP in patients with breast cancer. Methods This population-based cohort study used the Taiwan National Health Insurance Research Database. A cohort of 22 005 patients aged >= 20 years with breast cancer from January 1, 2000 to December 31, 2009 was identified and the date of cancer diagnosis was set as the index date. The end point was developing AP during the follow-up. Hazard ratios (HRs) and 95% confidence intervals (CIs) were evaluated to determine the correlation between the risk of AP and tamoxifen use. Because the drug use varied over time, it was measured as a time-dependent covariate in the Cox proportional hazard model. The same approaches were applied in PS-matched cohorts. Results After adjustment for covariates and medication use including fluorouracil and doxorubicin, the risk of AP was not significant between tamoxifen users and tamoxifen nonusers (adjusted HR = 0.94, 95% CI = 0.74-1.19) in the non-matching cohorts. The results revealed no dose-response trend between tamoxifen use and the risk of AP (adjusted HR = 0.98, 95% CI = 0.96-1.00). The comorbidities DM and gallstones were associated with a significantly increased risk of AP. Similar trends were observed in PS-matched cohorts. Conclusions No significant correlation was observed between tamoxifen use and the risk of AP in patients with breast cancer.
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页数:9
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