Statin use and breast cancer survival: a nationwide cohort study in Scotland

被引:46
|
作者
Mc Menamin, Una C. [1 ,4 ]
Murray, Liam J. [1 ,3 ]
Hughes, Carmel M. [2 ]
Cardwell, Chris R. [1 ]
机构
[1] Queens Univ Belfast, Ctr Publ Hlth, Canc Epidemiol & Hlth Serv Res Grp, Belfast, Antrim, North Ireland
[2] Queens Univ Belfast, Sch Pharm, Belfast BT9 7BL, Antrim, North Ireland
[3] Queens Univ Belfast, Ctr Publ Hlth, Ctr Excellence Publ Hlth NI, Belfast, Antrim, North Ireland
[4] Queens Univ Belfast, Inst Clin Sci, Royal Victoria Hosp, Block B, Belfast BT12 6BA, Antrim, North Ireland
来源
BMC CANCER | 2016年 / 16卷
关键词
Statins; Breast Cancer; Scotland; Pharmacoepidemiology; RECURRENCE; MORTALITY; STAGE; RISK; BIAS; SIMVASTATIN; DIAGNOSIS; CELLS; TIME;
D O I
10.1186/s12885-016-2651-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Preclinical evidence suggests that statins could delay cancer progression. Previous epidemiological findings have been inconsistent and some have been limited by small sample sizes, as well as certain time-related biases. This study aimed to investigate whether breast cancer patients who were exposed to statins had reduced breast cancer-specific mortality. Methods: We conducted a retrospective cohort study of 15,140 newly diagnosed invasive breast cancer patients diagnosed from 2009 to 2012 within the Scottish Cancer Registry. Dispensed medication usage was obtained from linkages to the Scottish Prescribing Information System and breast cancer-specific deaths were identified from National Records of Scotland Death Records. Using time-dependent Cox regression models, hazard ratios (HR) and 95 % confidence intervals (CI) were calculated for the association between post-diagnostic exposure to statins (including simvastatin) and breast cancer-specific mortality. Adjustments were made for a range of potential confounders including age at diagnosis, year of diagnosis, cancer stage, grade, cancer treatments received, comorbidities, socioeconomic status and use of aspirin. Results: A total of 1,190 breast cancer-specific deaths occurred up to January 2015. Overall, after adjustment for potential confounders, there was no evidence of an association between statin use and breast cancer-specific death (adjusted HR 0.93, 95 % CI 0.77, 1.12). No significant associations were observed in dose-response analyses or in analysis of all-cause mortality. For simvastatin use specifically, a weak non-significant reduction in breast cancer-specific mortality was observed compared to non-users (adjusted HR 0.89, 95 % CI 0.73, 1.08). Statin use before diagnosis was weakly associated with a reduction in breast cancer-specific mortality (adjusted HR 0.85, 95 % CI 0.74, 0.98). Conclusion: Overall, we found little evidence of a protective association between post-diagnostic statin use and cancer-specific mortality in a large nation-wide cohort of breast cancer patients. These findings will help inform the decision whether to conduct randomised controlled trials of statins as an adjuvant treatment in breast cancer.
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页数:11
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