Chang Chun-Hung, Chen Shaw-Ji, Liu Chieh-Yu
Department of Psychiatry, China Medical University Hospital, Taichung, Taiwan, ROC; Institute of Clinical Medicine, China Medical University, Taichung, Taiwan, ROC; Sunshine Psychiatric Hospital, Taichung, Taiwan, ROC.
Department of Psychiatry, Mackay Memorial Hospital Taitung Branch, Taitung, Taiwan, ROC; Mackay Junior College of Medicine, Nursing, and Management, Taipei, Taiwan, ROC; Institute of Medical Sciences, Tzu Chi university, Hualien, Taiwan, ROC.
J Affect Disord. 2015 Aug 15;182:44-9. doi: 10.1016/j.jad.2015.04.027. Epub 2015 Apr 23.
Previous studies have posited conflicting results regarding depressive disorders among breast cancer survivors who received adjuvant therapies including chemotherapy, radiotherapy, selective estrogen receptor modulator (e.g. tamoxifen), third-generation aromatase inhibitors (AIs; e.g. anastrozole, letrozole or exemestane), and monoclonal antibody (e.g. trastuzumab). We therefore performed a population-based study with a defined breast cancer cohort to investigate the risk of depressive disorders in breast cancer patients who received adjuvant therapies.
We conducted a retrospective study of a breast cancer cohort of 36,586 participants who were selected from the National Health Insurance Research Database(NHIRD) in Taiwan. Patients were observed for a maximum of 6 years to determine the incidences of newly onset depressive disorders. Kaplan-Meier and Cox regression analyses were used to identify the risk factors associated with depressive disorders in breast cancer patients who underwent adjuvant therapies
Of the total 36,586 patients, 1342 (3.7%) were ascertained with depressive disorders. The Cox multivariate proportional hazards analysis showed that age of 40-59 (adjusted hazard ratio (aHR) 1.327, 95% CI 1.123-1.567, p=0.001), chemotherapy (aHR 1.555, 95% CI 1.387-1.743, p<0.001), radiotherapy (aHR 1.385 95% CI 1.220-1.571, p<0.001), tamoxifen (aHR 1.458, 95% CI 1.110-1.914, p=0.007), AIs (aHR 1.360, 95% CI 1.193-1.550, p<0.001), and trastuzumab (aHR 1.458, 95% CI 1.110-1.914, p=0.007) were independent risk factors for developing depressive disorders.
The dosage effect of adjuvant treatments, cancer staging, genetic or environmental confounders associated with the risk of depressive disorders were not comprehensively evaluated.
Developing depressive disorders are at higher risk in breast cancer survivors aged 40-59 who received adjuvant treatments including chemotherapy, radiotherapy, tamoxifen, AIs or trastuzumab. Psychological evaluation and support are necessarily needed in breast cancer survivors who received adjuvant therapies.
先前的研究对于接受辅助治疗(包括化疗、放疗、选择性雌激素受体调节剂(如他莫昔芬)、第三代芳香化酶抑制剂(AIs;如来曲唑、阿那曲唑或依西美坦)以及单克隆抗体(如曲妥珠单抗))的乳腺癌幸存者中抑郁症的情况得出了相互矛盾的结果。因此,我们开展了一项基于人群的研究,以一个明确的乳腺癌队列来调查接受辅助治疗的乳腺癌患者患抑郁症的风险。
我们对从台湾国民健康保险研究数据库(NHIRD)中选取的36586名参与者组成的乳腺癌队列进行了一项回顾性研究。对患者进行最长6年的观察,以确定新发抑郁症的发生率。采用Kaplan-Meier法和Cox回归分析来确定接受辅助治疗的乳腺癌患者中与抑郁症相关的风险因素。
在总共36586名患者中,有1342名(3.7%)被确诊患有抑郁症。Cox多变量比例风险分析显示,年龄在40 - 59岁(调整后风险比(aHR)1.327,95%置信区间1.123 - 1.567,p = 0.001)、化疗(aHR 1.555,CI 1.387 - 1.743,p < 0.001)、放疗(aHR 1.385,95%置信区间1.220 - 1.571,p < 0.001)、他莫昔芬(aHR 1.458,95%置信区间1.110 - 1.914,p = 0.007)、AIs(aHR 1.360,95%置信区间1.193 - 1.550,p < 0.001)以及曲妥珠单抗(aHR 1.458,95%置信区间1.110 - 1.914,p = 0.007)是发生抑郁症的独立风险因素。
辅助治疗的剂量效应、癌症分期、与抑郁症风险相关的遗传或环境混杂因素未得到全面评估。
年龄在40 - 59岁且接受过包括化疗、放疗、他莫昔芬、AIs或曲妥珠单抗在内的辅助治疗的乳腺癌幸存者患抑郁症的风险更高。接受辅助治疗的乳腺癌幸存者需要进行心理评估和获得心理支持。