Ahmed K A, Abuodeh Y A, Echevarria M I, Arrington J A, Stallworth D G, Hogue C, Naghavi A O, Kim S, Kim Y, Patel B G, Sarangkasiri S, Johnstone P A S, Sahebjam S, Khushalani N I, Forsyth P A, Harrison L B, Yu M, Etame A B, Caudell J J
Department of Radiation Oncology.
Department of Radiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa.
Ann Oncol. 2016 Dec;27(12):2288-2294. doi: 10.1093/annonc/mdw417. Epub 2016 Sep 15.
The effect of immunologic and targeted agents on intracranial response rates in patients with melanoma brain metastases (MBMs) is not yet clearly understood. This report analyzes outcomes of intact MBMs treated with single-session stereotactic radiosurgery (SRS) and anti-PD-1 therapy, anti-CTLA-4 therapy, BRAF/MEK inhibitors(i), BRAFi, or conventional chemotherapy.
Patients were included if MBMs were treated with single-session SRS within 3 months of receiving systemic therapy. The primary end point of this study was distant MBM control. Secondary end points were local MBM control defined as a >20% volume increase on follow-up MRI, systemic progression-free survival, overall survival (OS) from both SRS and cranial metastases diagnosis, and neurotoxicity. Images were reviewed alongside two neuro-radiologists at our institution.
Ninety-six patients were treated to 314 MBMs over 119 SRS treatment sessions between January 2007 and August 2015. No significant differences were noted in age (P = 0.27), gender (P = 0.85), treated gross tumor volume (P = 0.26), or the diagnosis-specific graded prognostic assessment (P = 0.51) between the treatment cohorts. Twelve-month Kaplan-Meier (KM) distant MBM control rates were 38%, 21%, 20%, 8%, and 5% (P = 0.008) for SRS with anti-PD-1 therapies, anti-CTLA-4 therapy, BRAF/MEKi, BRAFi, and conventional chemotherapy, respectively. No significant differences were noted in the KM local MBM control rates among treatment groups (P = 0.25). Treatment with anti-PD-1 therapy, anti-CTLA-4 therapy, or BRAF/MEKi significantly improved OS on both univariate and multivariate analyses when compared with conventional chemotherapy.
In our institutional analysis of patients treated with SRS and various systemic immunologic and targeted melanoma agents, significant differences in distant MBM control and OS are noted. Prospective evaluation of the potential synergistic effect between these agents and SRS is warranted.
免疫治疗药物和靶向治疗药物对黑色素瘤脑转移(MBM)患者颅内反应率的影响尚不清楚。本报告分析了采用单次立体定向放射外科治疗(SRS)联合抗程序性死亡受体1(PD-1)治疗、抗细胞毒性T淋巴细胞相关抗原4(CTLA-4)治疗、BRAF/丝裂原活化蛋白激酶(MEK)抑制剂(i)、BRAF抑制剂(BRAFi)或传统化疗对完整MBM的治疗效果。
若MBM患者在接受全身治疗后3个月内接受单次SRS治疗,则纳入本研究。本研究的主要终点为远处MBM控制情况。次要终点包括局部MBM控制情况(定义为随访磁共振成像(MRI)显示体积增加>20%)、全身无进展生存期、自SRS和颅转移诊断后的总生存期(OS)以及神经毒性。图像由我院的两名神经放射科医生共同阅片。
2007年1月至2015年8月期间,119次SRS治疗共治疗了96例患者的314个MBM。各治疗组之间在年龄(P = 0.27)、性别(P = 0.85)、治疗的肿瘤总体积(P = 0.26)或诊断特异性分级预后评估(P = 0.51)方面均未观察到显著差异。采用SRS联合抗PD-1治疗、抗CTLA-4治疗、BRAF/MEK抑制剂、BRAF抑制剂和传统化疗的12个月Kaplan-Meier(KM)远处MBM控制率分别为38%、21%、20%、8%和5%(P = 0.008)。各治疗组之间的KM局部MBM控制率未观察到显著差异(P = 0.25)。与传统化疗相比,采用抗PD-1治疗、抗CTLA-4治疗或BRAF/MEK抑制剂治疗在单因素和多因素分析中均显著改善了OS。
在我们对接受SRS及各种全身免疫治疗和靶向黑色素瘤药物治疗的患者进行的机构分析中,观察到远处MBM控制和OS存在显著差异。有必要对这些药物与SRS之间潜在的协同效应进行前瞻性评估。