Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, USA.
Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Radiother Oncol. 2020 Oct;151:141-148. doi: 10.1016/j.radonc.2020.07.035. Epub 2020 Jul 24.
Immune checkpoint inhibitor with radiation therapy (ICI + RT) is under investigation for improved patient outcome, so we performed a systematic review/meta-analysis of toxicities for ICI + RT compared to immune checkpoint inhibitor (ICI) therapy alone.
A PRISMA-compliant systematic review of studies in MEDLINE (PubMed) and in the National Comprehensive Cancer Network guidelines was conducted, with primary outcome grade 3 + toxicity. Criteria for ICI alone were: phase III/IV trials that compared immunotherapy to placebo, chemotherapy, or alternative immunotherapy; and for ICI + RT: prospective/retrospective studies with an arm treated with ICI + RT. Meta-analysis was performed by random effects models using the DerSimonian and Laird method. The I statistic and Cochran's Q test were used to assess heterogeneity, while funnel plots and Egger's test assessed publication bias.
This meta-analysis included 51 studies (n = 15,398), with 35 ICI alone (n = 13,956) and 16 ICI + RT studies (n = 1,442). Our models showed comparable grade 3-4 toxicities in ICI + RT (16.3%; 95% CI, 11.1-22.3%) and ICI alone (22.3%; 95% CI, 18.1-26.9%). Stratification by timing of radiation and irradiated site showed no significant differences, but anti-CTLA-4 therapy and melanoma showed increased toxicity. The grade 5 toxicities were 1.1% and 1.9% for ICI alone and ICI + RT respectively. There was significant heterogeneity, but not publication bias.
The random effects model showed comparable grade 3-4 toxicity in using ICI + RT compared to ICI alone in CNS melanoma metastases, NSCLC, and prostate cancer. ICI + RT is safe for future clinical trials in these cancers.
免疫检查点抑制剂联合放疗(ICI+RT)在改善患者预后方面的研究正在进行中,因此我们对ICI+RT 与单独使用免疫检查点抑制剂(ICI)治疗的毒性进行了系统评价/荟萃分析。
我们对 MEDLINE(PubMed)和国家综合癌症网络指南中的研究进行了符合 PRISMA 标准的系统评价,主要结局为 3+级毒性。单独使用 ICI 的标准为:比较免疫治疗与安慰剂、化疗或其他免疫治疗的 III/IV 期试验;ICI+RT 的标准为:前瞻性/回顾性研究,其中一个臂接受 ICI+RT 治疗。使用随机效应模型和 DerSimonian 和 Laird 方法进行荟萃分析。使用 I 统计量和 Cochran's Q 检验评估异质性,而漏斗图和 Egger 检验评估发表偏倚。
本荟萃分析纳入了 51 项研究(n=15398),其中 35 项为单独使用 ICI(n=13956),16 项为 ICI+RT 研究(n=1442)。我们的模型显示,ICI+RT(16.3%;95%CI,11.1-22.3%)和单独使用 ICI(22.3%;95%CI,18.1-26.9%)的 3-4 级毒性相当。按放疗时间和照射部位分层,差异无统计学意义,但抗 CTLA-4 治疗和黑色素瘤显示毒性增加。单独使用 ICI 和 ICI+RT 的 5 级毒性分别为 1.1%和 1.9%。存在显著的异质性,但无发表偏倚。
随机效应模型显示,在 CNS 黑色素瘤转移、非小细胞肺癌和前列腺癌中,ICI+RT 与单独使用 ICI 相比,3-4 级毒性相当。ICI+RT 在这些癌症的未来临床试验中是安全的。