Impact of 5α-reductase inhibitor and α-blocker therapy for benign prostatic hyperplasia on prostate cancer incidence and mortality

被引:16
作者
Van Rompay, Maria I. [1 ]
Nickel, J. Curtis [2 ]
Ranganathan, Gayatri [1 ]
Kantoff, Philip W. [3 ]
Solomon, Keith R. [4 ,5 ,6 ,9 ]
Lund, Jennifer L. [7 ]
McKinlay, John B. [1 ,8 ]
机构
[1] HealthCore NERI, 480 Pleasant St,Suite A100, Watertown, MA 02472 USA
[2] Queens Univ, Kingston Gen Hosp, Kingston, ON, Canada
[3] Weill Cornell Med Coll, Mem Sloan Kettering Canc Ctr, New York, NY USA
[4] Harvard Med Sch, Dept Orthopaed Surg, Boston, MA 02115 USA
[5] Boston Childrens Hosp, Dept Orthopaed Surg, Boston, MA USA
[6] Boston Childrens Hosp, Dept Urol, Boston, MA USA
[7] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27515 USA
[8] Harvard Med Sch, Massachusetts Gen Hosp, Boston, MA 02115 USA
[9] Appl Photophys, 100 Cummings Ctr,Suite 440C, Beverly, MA 01915 USA
基金
美国国家卫生研究院;
关键词
benign prostatic hyperplasia; dutasteride; finasteride; adrenergic alpha-antagonists; prostatic neoplasms; pharmacoepidemiology; #ProstateCancer; HIGH-GRADE; FINASTERIDE; RISK; MEN; DUTASTERIDE; PREVENTION; SURVIVAL;
D O I
10.1111/bju.14534
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objective To investigate the use of 5 alpha-reductase inhibitors (5ARIs) and alpha-blockers among men with benign prostatic hyperplasia (BPH) in relation to prostate cancer (PCa) incidence, severity and mortality. Patients and Methods A retrospective 20-year cohort study in men residing in Saskatchewan, aged 40-89 years, with a BPH-coded medical claim between 1995 and 2014, was conducted. Cox proportional hazards regression was used to compare incidence of PCa diagnosis, metastatic PCa, Gleason score 8-10 PCa, and PCa mortality among 5ARI users (n = 4 571), alpha-blocker users (n = 7 764) and non-users (n = 11 677). Results In comparison with both non-users and alpha-blocker users, 5ARI users had a similar to 40% lower risk of a PCa diagnosis (11.0% and 11.4% vs 5.8%, respectively), and alpha-blocker users had an 11% lower risk of a PCa diagnosis compared with non-users. Overall, the incidence of metastatic PCa and PCa mortality was not significantly different among 5ARI or alpha-blocker users compared with non-users (adjusted hazard ratios [HR] of metastatic PCa: 1.12 and 1.13, respectively, and PCa mortality: 1.11 and 1.18, respectively, P > 0.05 for both drugs), but both 5ARI and a-blocker users had similar to 30% higher risk of Gleason score 8-10 cancer, adjusted HR 1.37, 95% confidence interval [CI] 1.03-1.82, P = 0.03, and adjusted HR 1.28, 95% CI 1.03-1.59, P = 0.02, respectively compared with non-users. Conclusion The use of 5ARIs was associated with lower risk of PCa diagnosis, regardless of comparison group. Risk of high grade PCa was higher among both 5ARI users and alpha-blocker users compared with non-users; however, this did not translate into higher risk of PCa mortality.
引用
收藏
页码:511 / 518
页数:8
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