Baik Seo Hyon, Kury Fabricio Sampaio Peres, McDonald Clement Joseph
All authors: US National Institutes of Health, Bethesda, MD.
J Clin Oncol. 2017 Oct 20;35(30):3401-3409. doi: 10.1200/JCO.2017.72.6109. Epub 2017 Aug 25.
Purpose To assess the relative risk of Alzheimer's disease (AD) among patients with prostate cancer who received androgen deprivation therapy (ADT), after adjustment for other cancer therapies. Methods Data from demographics, survival, diagnoses codes, procedure codes, and other information about beneficiaries age 67 years or older in the Medicare claims database was assessed to determine the unadjusted and adjusted risks of AD and of dementia from ADT. The prespecified survival analysis method was competing risk regression. Results Of the 1.2 million fee-for-service Medicare beneficiaries who developed prostate cancer in 2001 to 2014, 35% received ADT. Of these, 109,815 (8.9%) and 223,765 (18.8%) developed AD and dementia, respectively, and 26% to 33% died without either outcome. Unadjusted rates of AD and all-cause mortality per 1,000 patient-years were higher among ADT recipients; the unadjusted rates of AD were 17.0 and 15.5 per 1,000 person-years in recipients and nonrecipients, respectively, and the unadjusted rates of all-cause mortality were 73.0 and 51.6 per 1,000 person-years, respectively. The unadjusted rates for dementia in ADT recipients versus nonrecipients were 38.5 and 32.9, respectively, and the unadjusted rates of mortality were 60.2 versus 40.4, respectively. However, after analysis was adjusted for other cancer therapies and other covariates, patients with ADT treatment had no increased risk of AD (subdistribution hazard ratio [SHR], 0.98; 95% CI, 0.97 to 0.99) and had only a miniscule (1%) risk of dementia (SHR, 1.01; 95% CI, 1.01 to 1.02); patients treated with ADT were more likely to die before progression to AD (SHR, 1.24; 95% CI, 1.23 to 1.24) or dementia (SHR, 1.26; 95% CI, 1.25 to 1.26). The risks of AD and dementia were not associated with duration of ADT (ie, no dose effect). Other secondary analyses confirmed these results. Conclusion These data suggest that ADT treatment has no hazard for AD and no meaningful hazard for dementia among men age 67 years or older who are enrolled in Medicare.
目的 评估接受雄激素剥夺疗法(ADT)的前列腺癌患者在调整其他癌症治疗因素后的阿尔茨海默病(AD)相对风险。方法 对医疗保险理赔数据库中67岁及以上受益人的人口统计学、生存情况、诊断代码、程序代码及其他信息进行数据评估,以确定ADT导致AD和痴呆的未调整及调整后风险。预先设定的生存分析方法为竞争风险回归。结果 在2001年至2014年患前列腺癌的120万按服务收费的医疗保险受益人中,35%接受了ADT。其中,分别有109,815人(8.9%)和223,765人(18.8%)患上了AD和痴呆,26%至33%的人在未出现这两种结局的情况下死亡。ADT接受者中每1000患者年的AD和全因死亡率的未调整率较高;接受者和未接受者中AD的未调整率分别为每1000人年17.0和15.5,全因死亡率的未调整率分别为每1000人年73.0和51.6。ADT接受者与未接受者相比,痴呆的未调整率分别为38.5和32.9,死亡率的未调整率分别为60.2和40.4。然而,在对其他癌症治疗和其他协变量进行分析调整后,接受ADT治疗的患者患AD的风险没有增加(亚分布风险比[SHR],0.98;95%置信区间,0.97至0.99),患痴呆的风险仅微小增加(1%)(SHR,1.01;95%置信区间,1.01至1.02);接受ADT治疗的患者在进展为AD(SHR,1.24;95%置信区间,1.23至1.24)或痴呆(SHR,1.26;95%置信区间,1.25至1.26)之前更有可能死亡。AD和痴呆的风险与ADT持续时间无关(即无剂量效应)。其他二次分析证实了这些结果。结论 这些数据表明,对于参加医疗保险的67岁及以上男性,ADT治疗对AD无危害,对痴呆也无显著危害。