Gramatzki Dorothee, Rogers James Louis, Neidert Marian Christoph, Hertler Caroline, Le Rhun Emilie, Roth Patrick, Weller Michael
Department of Neurology & Brain Tumor Center, Clinical Neuroscience Center, University Hospital and University of Zurich, Switzerland.
Department of Neurosurgery, Clinical Neuroscience Center, University Hospital Zurich and University of Zurich, Switzerland.
Neurooncol Pract. 2020 Apr 25;7(5):514-521. doi: 10.1093/nop/npaa022. eCollection 2020 Oct.
Antidepressant drugs have shown antitumor activity in preclinical glioblastoma studies. Antidepressant drug use, as well as its association with survival, in glioblastoma patients has not been well characterized on a population level.
Patient characteristics, including the frequency of antidepressant drug use, were assessed in a glioblastoma cohort diagnosed in a 10-year time frame between 2005 and 2014 in the Canton of Zurich, Switzerland. Cox proportional hazards regression models were applied for multivariate analysis. Kaplan-Meier survival curves were used to estimate overall survival (OS) data and the log-rank test was performed for comparisons.
A total of 404 patients with isocitrate dehydrogenase wild-type glioblastoma were included in this study. Sixty-five patients (16.1%) took antidepressant drugs at some point during the disease course. Patients were most commonly prescribed selective serotonin reuptake inhibitors at any time (N = 46, 70.8%). Nineteen patients (29.2%) were on antidepressant drugs at the time of their tumor diagnosis. No differences were observed in OS between those patients who had taken antidepressants at some point in their disease course and those who had not ( = .356). These data were confirmed in a multivariate analysis including age, Karnofsky Performance Scale (KPS), sex, extent of resection, O-methylguanine DNA methyltransferase () promoter methylation status, and first-line treatment as cofounders ( = .315). Also, there was no association of use of drugs modulating voltage-dependent potassium channels (citalopram; escitalopram) with survival ( = .639).
This signal-seeking study does not support the hypothesis that antidepressants have antitumor efficacy in glioblastoma on a population level.
在临床前胶质母细胞瘤研究中,抗抑郁药物已显示出抗肿瘤活性。在胶质母细胞瘤患者中,抗抑郁药物的使用情况及其与生存率的关联在人群层面尚未得到充分描述。
对2005年至2014年期间在瑞士苏黎世州诊断的胶质母细胞瘤队列患者的特征进行评估,包括抗抑郁药物的使用频率。采用Cox比例风险回归模型进行多变量分析。使用Kaplan-Meier生存曲线估计总生存(OS)数据,并进行对数秩检验以作比较。
本研究共纳入404例异柠檬酸脱氢酶野生型胶质母细胞瘤患者。65例患者(16.1%)在病程中的某个时间点服用过抗抑郁药物。患者在任何时候最常被处方的是选择性5-羟色胺再摄取抑制剂(N = 46,70.8%)。19例患者(29.2%)在肿瘤诊断时正在服用抗抑郁药物。在病程中某个时间点服用过抗抑郁药物的患者与未服用过的患者之间,总生存情况未观察到差异(P = 0.356)。在一项多变量分析中,纳入年龄、卡氏功能状态评分(KPS)、性别、切除范围、O-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化状态及一线治疗作为协变量后,这些数据得到了证实(P = 0.315)。此外,使用调节电压依赖性钾通道的药物(西酞普兰;艾司西酞普兰)与生存率之间也无关联(P = 0.639)。
这项探索性研究不支持抗抑郁药物在人群层面上对胶质母细胞瘤具有抗肿瘤疗效这一假设。