Testosterone treatment and the risk of aggressive prostate cancer in men with low testosterone levels

被引:30
|
作者
Walsh, Thomas J. [1 ,2 ]
Shores, Molly M. [1 ,2 ]
Krakauer, Chloe A. [2 ]
Forsberg, Christopher W. [2 ]
Fox, Alexandra E. [2 ]
Moore, Kathryn P. [2 ]
Korpak, Anna [2 ]
Heckbert, Susan R. [1 ,3 ]
Zeliadt, Steven B. [2 ]
Kinsey, Chloe E. [2 ]
Thompson, Mary Lou [1 ,2 ]
Smith, Nicholas L. [1 ,2 ,3 ]
Matsumoto, Alvin M. [2 ,4 ,5 ]
机构
[1] Univ Washington, Seattle, WA 98195 USA
[2] VA Puget Sound Hlth Care Syst, Seattle, WA 98108 USA
[3] Grp Hlth Cooperat Puget Sound, Grp Hlth Res Inst, Seattle, WA USA
[4] Univ Washington, Sch Med, Dept Med, Div Gerontol & Geriatr Med, Seattle, WA 98195 USA
[5] VA Puget Sound Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Seattle, WA USA
来源
PLOS ONE | 2018年 / 13卷 / 06期
基金
美国国家卫生研究院;
关键词
REPLACEMENT THERAPY; HYPOGONADAL MEN; ANDROGEN DEFICIENCY; OLDER MEN; PREVALENCE; METAANALYSIS; OUTCOMES; ANTIGEN; TRENDS; SAFETY;
D O I
10.1371/journal.pone.0199194
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
Purpose Testosterone treatment of men with low testosterone is common and, although relatively short-term, has raised concern regarding an increased risk of prostate cancer (CaP). We investigated the association between modest-duration testosterone treatment and incident aggressive CaP. Materials and methods Retrospective inception cohort study of male Veterans aged 40 to 89 years with a laboratory-defined low testosterone measurement from 2002 to 2011 and recent prostate specific antigen (PSA) testing; excluding those with recent testosterone treatment, prostate or breast cancer, high PSA or prior prostate biopsy. Histologically-confirmed incident aggressive prostate cancer or any prostate cancer were the primary and secondary outcomes, respectively. Results Of the 147,593 men included, 58,617 were treated with testosterone. 313 aggressive CaPs were diagnosed, 190 among untreated men (incidence rate (IR) 0.57 per 1000 person years, 95% CI 0.49-0.65) and 123 among treated men (IR 0.58 per 1000 person years; 95% CI 0.48-0.69). After adjusting for age, race, hospitalization during year prior to cohort entry, geography, BMI, medical comorbidities, repeated testosterone and PSA testing, testosterone treatment was not associated with incident aggressive CaP (HR 0.89; 95% CI 0.70-1.13) or any CaP (HR 0.90; 95% CI 0.81-1.01). No association between cumulative testosterone dose or formulation and CaP was observed. Conclusions Among men with low testosterone levels and normal PSA, testosterone treatment was not associated with an increased risk of aggressive or any CaP. The clinical risks and benefits of testosterone treatment can only be fully addressed by large, longer-term randomized controlled trials.
引用
收藏
页数:24
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