Testosterone therapy and cancer risk

被引:18
作者
Eisenberg, Michael L. [1 ,2 ]
Li, Shufeng [1 ,3 ]
Betts, Paul [4 ]
Herder, Danielle [5 ]
Lamb, Dolores J. [5 ]
Lipshultz, Larry I. [5 ]
机构
[1] Stanford Univ, Sch Med, Dept Urol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Obstet Gynecol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Dermatol, Stanford, CA 94305 USA
[4] Texas Dept State Hlth Serv, Texas Canc Registry, Canc Epidemiol & Surveillance Branch, Austin, TX USA
[5] Baylor Coll Med, Scott Dept Urol, Houston, TX 77030 USA
关键词
testosterone; hypogonadism; neoplasms; PROSTATE-SPECIFIC ANTIGEN; LOW SERUM TESTOSTERONE; HYPOGONADAL MEN; REPLACEMENT THERAPY; TESTIM REGISTRY; OLDER MEN; SEXUAL FUNCTION; US TRIUS; MORTALITY; MASS;
D O I
10.1111/bju.12756
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 determine if testosterone therapy (TT) status modifies a man's risk of cancer. Patients and Methods The Urology clinic hormone database was queried for all men with a serum testosterone level and charts examined to determine TT status. Patient records were linked to the Texas Cancer Registry to determine the incidence of cancer. Men accrued time at risk from the date of initiating TT or the first office visit for men not on TT. Standardised incidence rates and time to event analysis were performed. Results In all, 247 men were on TT and 211 did not use testosterone. In all, 47 men developed cancer, 27 (12.8%) were not on TT and 20 (8.1%) on TT. There was no significant difference in the risk of cancer incidence based on TT (hazard ratio [HR] 1.0, 95% confidence interval [CI] 0.57-1.9; P = 1.8). There was no difference in prostate cancer risk based on TT status (HR 1.2, 95% CI 0.54-2.50). Conclusion There was no change in cancer risk overall, or prostate cancer risk specifically, for men aged >40 years using long-term TT.
引用
收藏
页码:317 / 321
页数:5
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