Department of Radiation Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia.
Department of Biostatistics & Bioinformatics, Rollins School of Public Heath, Emory University, Atlanta, Georgia.
Int J Radiat Oncol Biol Phys. 2020 Sep 1;108(1):304-313. doi: 10.1016/j.ijrobp.2019.12.030. Epub 2020 Jan 24.
Radical treatment of metastases with stereotactic body radiation therapy (SBRT) is commonly implemented in patients receiving concurrent immune checkpoint inhibition (ICI), despite limited safety and toxicity data. The purpose of this study was to evaluate the safety and tolerability of lung SBRT with concurrent ICI.
Records from a single academic institution were reviewed to identify patients treated with lung SBRT and concurrent (within 30 days) ICI; a contemporaneous cohort receiving lung SBRT alone was included for reference. Treatment-related adverse effects occurring within 30 days (acute) and 180 days (subacute) of SBRT were evaluated.
Our study included 117 patients; 54 received SBRT with concurrent ICI (56 courses, 69 target lesions), and 63 received SBRT alone (68 courses, 79 lesions). Median follow-up was 9.2 months in the SBRT + ICI cohort. Among the patients, 67.9% received ICI monotherapy, 17.9% ICI/chemotherapy, and 14.3% ICI/ICI combinations; 25% received ICI between SBRT fractions, and 42.9% received ICI both before and after SBRT. The risk of grade 3 pneumonitis was higher in the SBRT + ICI versus SBRT alone cohort (10.7% vs 0%, P < .01) and any-grade pneumonitis was similar (33.9% vs 27.9%, SBRT + ICI vs SBRT, P = .47). The risk of any-grade pneumonitis appeared elevated with ICI/ICI combinations (62.5% vs 29.2%). Receipt of ICI, planning treatment volume, and lobes involved in SBRT were linked to high-grade pneumonitis. Subacute grade 3+ adverse effects occurred in 26.8% of SBRT + ICI and 2.9% of SBRT-alone patients.
Overall, concurrent lung SBRT + ICI is safe. Given the clinically meaningful risk of pneumonitis, closer monitoring should be considered for SBRT + ICI patients, especially those receiving radiation therapy with ICI/ICI combinations.
立体定向体部放射治疗(SBRT)根治转移性肿瘤,在接受免疫检查点抑制(ICI)治疗的患者中较为常见,尽管安全性和毒性数据有限。本研究的目的是评估同步 ICI 肺 SBRT 的安全性和耐受性。
对单机构的记录进行了回顾,以确定接受肺 SBRT 联合(30 天内)ICI 治疗的患者;同时纳入了同期接受单纯肺 SBRT 治疗的患者作为参考。评估 SBRT 后 30 天(急性)和 180 天(亚急性)内与治疗相关的不良反应。
本研究共纳入 117 例患者;54 例患者接受了 SBRT 联合 ICI(56 个疗程,69 个靶病灶),63 例患者接受了单纯 SBRT(68 个疗程,79 个病灶)。SBRT+ICI 组的中位随访时间为 9.2 个月。患者中,67.9%接受 ICI 单药治疗,17.9%接受 ICI/化疗,14.3%接受 ICI/ICI 联合治疗;25%在 SBRT 分次照射期间接受 ICI,42.9%在 SBRT 前后均接受 ICI。SBRT+ICI 组的 3 级肺炎发生率高于单纯 SBRT 组(10.7% vs 0%,P<.01),但任何级别的肺炎发生率相似(33.9% vs 27.9%,SBRT+ICI vs SBRT,P=.47)。ICI/ICI 联合治疗组任何级别的肺炎发生率较高(62.5% vs 29.2%)。接受 ICI、计划治疗体积和 SBRT 涉及的肺叶与高级别肺炎有关。SBRT+ICI 组有 26.8%的患者出现亚急性 3 级以上不良反应,单纯 SBRT 组有 2.9%的患者出现该不良反应。
总体而言,同步肺 SBRT+ICI 是安全的。鉴于肺炎的临床意义显著,SBRT+ICI 患者应密切监测,特别是接受 ICI/ICI 联合治疗的患者。