Bang Andrew, Wilhite Tyler J, Pike Luke R G, Cagney Daniel N, Aizer Ayal A, Taylor Allison, Spektor Alexander, Krishnan Monica, Ott Patrick A, Balboni Tracy A, Hodi F Stephen, Schoenfeld Jonathan D
Department of Radiation Oncology, Brigham and Women's Hospital/Dana-Farber Cancer Institute, Boston, Massachusetts; Division of Radiation Oncology, University of Ottawa, Ottawa, Ontario, Canada.
Harvard Medical School, Boston, Massachusetts.
Int J Radiat Oncol Biol Phys. 2017 Jun 1;98(2):344-351. doi: 10.1016/j.ijrobp.2017.02.003. Epub 2017 Feb 11.
To analyze immune-related adverse events (ir-AEs) in patients treated with radiation and immune checkpoint blockade.
We retrospectively reviewed records from patients with metastatic non-small cell lung cancer, melanoma, or renal cell cancer who received at least 1 cycle of a CTLA-4 or PD-1 inhibitor and radiation. Immune-related adverse events, defined using Common Terminology Criteria for Adverse Events version 4.0, were tabulated in relation to treatment variables, and associations with sequencing and timing were assessed.
We identified 133 patients, of whom 28 received a CTLA-4 inhibitor alone, 88 received a PD-1 inhibitor alone, and 17 received both classes of inhibitors either sequentially (n=13) or concurrently (n=4). Fifty-six patients received radiation within 14 days of an immune checkpoint inhibitor. Forty-six patients experienced at least 1 ir-AE (34.6%). Patients receiving both CTLA-4 and PD-1 inhibitors experienced more any-grade ir-AEs as compared with either individually (71% vs 29%, P=.0008). Any-grade ir-AEs occurred in 39% of patients in whom radiation was administered within 14 days of immunotherapy, compared with 23% of other patients (P=.06) and more often in patients who received higher equivalent dose in 2-Gy fractions (EQD2) EQD2 (P=.01). However, most toxicities were mild. There were no associations between site irradiated and specific ir-AEs.
Our data suggest the combination of focal palliative radiation and CTLA-4 and/or PD-1 inhibitors is well tolerated, with manageable ir-AEs that did not seem to be associated with the particular site irradiated. Although conclusions are limited by the heterogeneity of patients and treatments, and future confirmatory studies are needed, this information can help guide clinical practice for patients receiving immune checkpoint therapy who require palliative radiation therapy.
分析接受放疗和免疫检查点阻断治疗的患者的免疫相关不良事件(ir-AEs)。
我们回顾性分析了转移性非小细胞肺癌、黑色素瘤或肾细胞癌患者的记录,这些患者接受了至少1个周期的CTLA-4或PD-1抑制剂及放疗。使用不良事件通用术语标准第4.0版定义的免疫相关不良事件,根据治疗变量进行列表,并评估与治疗顺序和时间的相关性。
我们确定了133例患者,其中28例仅接受CTLA-4抑制剂,88例仅接受PD-1抑制剂,17例先后(n = 13)或同时(n = 4)接受两类抑制剂。56例患者在免疫检查点抑制剂治疗的14天内接受了放疗。46例患者发生了至少1次ir-AE(34.6%)。与单独使用CTLA-4或PD-1抑制剂相比,同时接受这两种抑制剂的患者发生任何级别的ir-AE的比例更高(71%对29%,P = 0.0008)。在免疫治疗14天内接受放疗的患者中,39%发生了任何级别的ir-AE,而其他患者为23%(P = 0.06),且在接受更高等效剂量(以2 Gy分割)的患者中更常见(P = 0.01)。然而,大多数毒性反应较轻。照射部位与特定的ir-AE之间无相关性。
我们的数据表明,局部姑息性放疗与CTLA-4和/或PD-1抑制剂联合使用耐受性良好,ir-AEs可控,且似乎与特定的照射部位无关。尽管结论受患者和治疗的异质性限制,且需要未来的验证性研究,但这些信息有助于指导接受免疫检查点治疗且需要姑息性放疗的患者的临床实践。