Loeb Stacy, Folkvaljon Yasin, Damber Jan-Erik, Alukal Joseph, Lambe Mats, Stattin Pär
Stacy Loeb and Joseph Alukal, New York University, New York, NY; Yasin Folkvaljon, Uppsala University Hospital; Pär Stattin, Uppsala University, Uppsala; Jan-Erik Damber, University of Gothenburg, Gothenburg; Mats Lambe, Karolinska Institutet, Stockholm; and Pär Stattin, Umeå University Hospital, Umeå, Sweden.
J Clin Oncol. 2017 May 1;35(13):1430-1436. doi: 10.1200/JCO.2016.69.5304. Epub 2017 Mar 13.
Purpose The association between exposure to testosterone replacement therapy (TRT) and prostate cancer risk is controversial. The objective was to examine this association through nationwide, population-based registry data. Methods We performed a nested case-control study in the National Prostate Cancer Register of Sweden, which includes all 38,570 prostate cancer cases diagnosed from 2009 to 2012, and 192,838 age-matched men free of prostate cancer. Multivariable conditional logistic regression was used to examine associations between TRT and risk of prostate cancer (overall, favorable, and aggressive). Results Two hundred eighty-four patients with prostate cancer (1%) and 1,378 control cases (1%) filled prescriptions for TRT. In multivariable analysis, no association was found between TRT and overall prostate cancer risk (odds ratio [OR], 1.03; 95% CI, 0.90 to 1.17). However, patients who received TRT had more favorable-risk prostate cancer (OR, 1.35; 95% CI, 1.16 to 1.56) and a lower risk of aggressive prostate cancer (OR, 0.50; 95% CI, 0.37 to 0.67). The increase in favorable-risk prostate cancer was already observed within the first year of TRT (OR, 1.61; 95% CI, 1.10 to 2.34), whereas the lower risk of aggressive disease was observed after > 1 year of TRT (OR, 0.44; 95% CI, 0.32 to 0.61). After adjusting for previous biopsy findings as an indicator of diagnostic activity, TRT remained significantly associated with more favorable-risk prostate cancer and lower risk of aggressive prostate cancer. Conclusion The early increase in favorable-risk prostate cancer among patients who received TRT suggests a detection bias, whereas the decrease in risk of aggressive prostate cancer is a novel finding that warrants further investigation.
目的 睾酮替代疗法(TRT)与前列腺癌风险之间的关联存在争议。本研究的目的是通过全国性的基于人群的登记数据来探讨这种关联。方法 我们在瑞典国家前列腺癌登记处进行了一项巢式病例对照研究,该登记处纳入了2009年至2012年诊断的所有38570例前列腺癌病例,以及192838例年龄匹配的无前列腺癌男性。采用多变量条件逻辑回归分析来研究TRT与前列腺癌风险(总体、预后良好和侵袭性)之间的关联。结果 284例前列腺癌患者(1%)和1378例对照(1%)开具了TRT处方。在多变量分析中,未发现TRT与总体前列腺癌风险之间存在关联(比值比[OR],1.03;95%可信区间[CI],0.90至1.17)。然而,接受TRT的患者患预后良好风险前列腺癌的比例更高(OR,1.35;95%CI,1.16至1.56),而侵袭性前列腺癌的风险较低(OR,0.50;95%CI,0.37至0.67)。在TRT的第一年就已观察到预后良好风险前列腺癌的增加(OR,1.6