An Yi, Jiang Wen, Kim Betty Y S, Qian Jack M, Tang Chad, Fang Penny, Logan Jennifer, D'Souza Neil M, Haydu Lauren E, Wang Xin A, Hess Kenneth R, Kluger Harriet, Glitza Isabella C, Mahajan Anita, Welsh James W, Lin Steven H, Yu James B, Davies Michael A, Hwu Patrick, Sulman Erik P, Brown Paul D, Chiang Veronica L S, Li Jing
Department of Therapeutic Radiology, Yale University School of Medicine, Yale-New Haven Hospital, United States.
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, United States.
Radiother Oncol. 2017 Oct;125(1):80-88. doi: 10.1016/j.radonc.2017.08.009. Epub 2017 Sep 12.
Numerous studies suggest that radiation can boost antitumor immune response by stimulating release of tumor-specific antigens. However, the optimal timing between radiotherapy and immune checkpoint blockade to achieve potentially synergistic benefits is unclear.
Multi-institutional retrospective analysis was conducted of ninety-nine metastatic melanoma patients from 2007 to 2014 treated with ipilimumab who later received stereotactic radiosurgery (SRS) for new brain metastases that developed after starting immunotherapy. All patients had complete blood count acquired before SRS. Primary outcomes were intracranial disease control and overall survival (OS).
The median follow-up time was 15.5months. In the MD Anderson cohort, patients who received SRS after 5.5months (n=20) of their last dose of ipilimumab had significantly worse intracranial control than patients who received SRS within 5.5months (n=51) (median 3.63 vs. 8.09months; hazard ratio [HR] 2.07, 95% confidence interval [CI] 1.03-4.16, p=0.041). OS was not different between the two arms. The improvement in intracranial control was confirmed in an independent validation cohort of 28 patients treated at Yale-New Haven Hospital. Circulating absolute lymphocyte count before SRS predicted for treatment response as those with baseline counts >1000/µL had reduced risk of intracranial recurrence compared with those with ≤1000/µL (HR 0.46, 95% CI 0.0.23-0.94, p=0.03).
In this multi-institutional study, patients who received SRS for new brain metastases within 5.5months after ipilimumab therapy had better intracranial disease control than those who received SRS later. Moreover, higher circulating lymphocyte count was associated with improved intracranial disease control.
众多研究表明,辐射可通过刺激肿瘤特异性抗原的释放来增强抗肿瘤免疫反应。然而,放疗与免疫检查点阻断之间实现潜在协同效益的最佳时机尚不清楚。
对2007年至2014年接受伊匹单抗治疗、后来因免疫治疗开始后出现的新发脑转移而接受立体定向放射外科治疗(SRS)的99例转移性黑色素瘤患者进行了多机构回顾性分析。所有患者在SRS前均进行了全血细胞计数。主要结局为颅内疾病控制和总生存期(OS)。
中位随访时间为15.5个月。在MD安德森队列中,末次剂量伊匹单抗5.5个月后接受SRS的患者(n = 20)的颅内控制情况明显差于末次剂量伊匹单抗5.5个月内接受SRS的患者(n = 51)(中位时间3.63个月对8.09个月;风险比[HR] 2.07,95%置信区间[CI] 1.03 - 4.16,p = 0.041)。两组的OS无差异。在耶鲁 - 纽黑文医院治疗的28例患者的独立验证队列中,证实了颅内控制情况的改善。SRS前的循环绝对淋巴细胞计数可预测治疗反应,因为基线计数>1000/µL的患者与≤1000/µL的患者相比,颅内复发风险降低(HR 0.46,95% CI 0.23 - 0.94,p = 0.03)。
在这项多机构研究中,伊匹单抗治疗后5.5个月内接受SRS治疗新发脑转移的患者比之后接受SRS的患者具有更好的颅内疾病控制。此外,较高的循环淋巴细胞计数与改善的颅内疾病控制相关。