Dinh Kathryn T, Reznor Gally, Muralidhar Vinayak, Mahal Brandon A, Nezolosky Michelle D, Choueiri Toni K, Hoffman Karen E, Hu Jim C, Sweeney Christopher J, Trinh Quoc-Dien, Nguyen Paul L
Kathryn T. Dinh, Vinayak Muralidhar, and Brandon A. Mahal, Harvard Medical School; Gally Reznor, Brandon A. Mahal, Michelle D. Nezolosky, Toni K. Choueiri, Christopher J. Sweeney, and Paul L. Nguyen, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Harvard Medical School; Quoc-Dien Trinh, Brigham and Women's Hospital, Harvard Medical School, Boston, MA; Karen E. Hoffman, The University of Texas MD Anderson Cancer Center, Houston, TX; and Jim C. Hu, Weill Cornell Medical College, James Buchanan Brady Foundation, New York, NY.
J Clin Oncol. 2016 Jun 1;34(16):1905-12. doi: 10.1200/JCO.2015.64.1969. Epub 2016 Apr 11.
Androgen deprivation therapy (ADT) may contribute to depression, yet several studies have not demonstrated a link. We aimed to determine whether receipt of any ADT or longer duration of ADT for prostate cancer (PCa) is associated with an increased risk of depression.
We identified 78,552 men older than age 65 years with stage I to III PCa using the SEER-Medicare-linked database from 1992 to 2006, excluding patients with psychiatric diagnoses within the prior year. Our primary analysis was the association between pharmacologic ADT and the diagnosis of depression or receipt of inpatient or outpatient psychiatric treatment using Cox proportional hazards regression. Drug data for treatment of depression were not available. Our secondary analysis investigated the association between duration of ADT and each end point.
Overall, 43% of patients (n = 33,882) who received ADT, compared with patients who did not receive ADT, had higher 3-year cumulative incidences of depression (7.1% v 5.2%, respectively), inpatient psychiatric treatment (2.8% v 1.9%, respectively), and outpatient psychiatric treatment (3.4% v 2.5%, respectively; all P < .001). Adjusted Cox analyses demonstrated that patients with ADT had a 23% increased risk of depression (adjusted hazard ratio [AHR], 1.23; 95% CI, 1.15 to 1.31), 29% increased risk of inpatient psychiatric treatment (AHR, 1.29; 95% CI, 1.17 to 1.41), and a nonsignificant 7% increased risk of outpatient psychiatric treatment (AHR, 1.07; 95% CI, 0.97 to 1.17) compared with patients without ADT. The risk of depression increased with duration of ADT, from 12% with ≤ 6 months of treatment, 26% with 7 to 11 months of treatment, to 37% with ≥ 12 months of treatment (P trend < .001). A similar duration effect was seen for inpatient (P trend < .001) and outpatient psychiatric treatment (P trend < .001).
Pharmacologic ADT increased the risk of depression and inpatient psychiatric treatment in this large study of elderly men with localized PCa. This risk increased with longer duration of ADT. The possible psychiatric effects of ADT should be recognized by physicians and discussed with patients before initiating treatment.
雄激素剥夺疗法(ADT)可能导致抑郁,但多项研究尚未证实两者之间存在关联。我们旨在确定接受任何ADT或较长时间的前列腺癌(PCa)ADT治疗是否与抑郁风险增加相关。
我们使用1992年至2006年的SEER-医疗保险关联数据库,识别出78552名年龄在65岁以上、患有I至III期PCa的男性,排除前一年有精神疾病诊断的患者。我们的主要分析是使用Cox比例风险回归分析药物性ADT与抑郁诊断或接受住院或门诊精神科治疗之间的关联。没有可用于治疗抑郁症的药物数据。我们的次要分析调查了ADT持续时间与每个终点之间的关联。
总体而言,接受ADT的患者中有43%(n = 33882),与未接受ADT的患者相比,3年累积抑郁发病率更高(分别为7.1%和5.2%)、住院精神科治疗(分别为2.8%和1.9%)以及门诊精神科治疗(分别为3.4%和2.5%;所有P <.001)。校正后的Cox分析表明,与未接受ADT的患者相比,接受ADT的患者抑郁风险增加23%(校正风险比[AHR],1.23;95%CI,1.15至1.31),住院精神科治疗风险增加29%(AHR,1.29;95%CI,1.17至1.41),门诊精神科治疗风险增加7%(无统计学意义;AHR,1.07;95%CI,0.97至1.17)。抑郁风险随着ADT持续时间的增加而增加,治疗≤6个月时为12%,7至11个月时为26%,≥12个月时为37%(P趋势<.001)。住院(P趋势<.001)和门诊精神科治疗(P趋势<.001)也观察到类似的持续时间效应。
在这项针对老年局限性PCa男性的大型研究中,药物性ADT增加了抑郁和住院精神科治疗的风险。这种风险随着ADT持续时间的延长而增加。医生在开始治疗前应认识到ADT可能的精神影响并与患者进行讨论。