Department of Epidemiology, Human Genetics, and Environmental Science, School of Public Health, University of Texas Health Science Center at Houston, Houston, Texas.
Department of Management Policy and Community Health, School of Public Health, University of Texas Health Science Center at Houston, Houston, Texas.
Pharmacotherapy. 2018 Oct;38(10):999-1009. doi: 10.1002/phar.2168. Epub 2018 Sep 4.
To examine the risks and compare the occurrences of major long-term side effects (sexual dysfunction, bone fractures, diabetes, cardiovascular morbidity, acute myocardial infarction [MI], and dementia) in patients with prostate cancer who received androgen-deprivation therapy (ADT) with those who did not.
Propensity score-matched retrospective cohort study using Medicare claims data.
National Cancer Institute's Surveillance, Epidemiology, and End Results Program-Medicare linked database.
A total of 201,797 patients 66 years or older who were diagnosed with any stage of prostate cancer between 1992 and 2009; of these, 94,528 patients received ADT; 107,269 patients did not.
We identified receipt of ADT and number of claims for ADT, and ascertained the long-term treatment-related side effects that occurred during 19 years of follow-up, from 1992-2010, from Medicare claims data. Cox proportional hazards models were used to estimate the incidences and hazard ratios (HRs) of newly developed side effects. Among all potential long-term side effects, the risk of bone fractures was highest (HR 1.39, 95% confidence interval [CI] 1.35-1.43), followed by diabetes (HR 1.21, 95% CI 1.18-1.24), dementia (HR 1.16, 95% CI 1.13-1.20), coronary heart disease (HR 1.12, 95% CI 1.09-1.14), and acute MI (HR 1.11, 95% CI 1.08-1.15) in those who received ADT compared with those who did not. The HRs for bone fractures and diabetes increased steadily as the number of ADT doses increased, indicating a linear trend in the dose-response relationship. Compared with patients who received active surveillance, ADT was associated with a 12% increased risk of sexual dysfunction (HR 1.12, 95% CI 1.05-1.20). The HR for sexual dysfunction increased to 1.68 (95% CI 1.59-1.77) when ADT was combined with radiation therapy and to 3.54 (95% CI 3.26-3.85) when ADT was combined with radiation and surgery.
The results of this study demonstrated that in men with prostate cancer, receipt of ADT was associated with higher risks of bone fractures, diabetes, dementia, coronary heart disease, acute MI, and sexual dysfunction than in those who did not receive ADT.
研究接受去势治疗(ADT)与未接受 ADT 的前列腺癌患者发生主要长期副作用(性功能障碍、骨折、糖尿病、心血管发病率、急性心肌梗死[MI]和痴呆)的风险和发生率。
使用医疗保险索赔数据进行倾向评分匹配回顾性队列研究。
国家癌症研究所的监测、流行病学和最终结果计划-医疗保险联合数据库。
1992 年至 2009 年间被诊断患有任何阶段前列腺癌且年龄在 66 岁或以上的共 201797 名患者;其中 94528 名患者接受 ADT;107269 名患者未接受 ADT。
我们从医疗保险索赔数据中确定了 ADT 的使用和 ADT 的索赔次数,并确定了在 19 年的随访期间(1992-2010 年)发生的长期治疗相关副作用。使用 Cox 比例风险模型估计新发生副作用的发生率和风险比(HR)。在所有潜在的长期副作用中,骨折风险最高(HR 1.39,95%置信区间[CI] 1.35-1.43),其次是糖尿病(HR 1.21,95% CI 1.18-1.24)、痴呆(HR 1.16,95% CI 1.13-1.20)、冠心病(HR 1.12,95% CI 1.09-1.14)和急性 MI(HR 1.11,95% CI 1.08-1.15)在接受 ADT 的患者中比未接受 ADT 的患者高。随着 ADT 剂量的增加,骨折和糖尿病的 HR 呈稳步上升趋势,表明剂量-反应关系呈线性趋势。与接受主动监测的患者相比,ADT 与性功能障碍风险增加 12%(HR 1.12,95% CI 1.05-1.20)相关。当 ADT 联合放疗时,性功能障碍的 HR 增加到 1.68(95% CI 1.59-1.77),当 ADT 联合放疗和手术时,HR 增加到 3.54(95% CI 3.26-3.85)。
这项研究的结果表明,在患有前列腺癌的男性中,与未接受 ADT 的患者相比,接受 ADT 与骨折、糖尿病、痴呆、冠心病、急性 MI 和性功能障碍的风险增加相关。