Liao Guixiang, Qian Yuting, Arooj Sumbal, Zhao Zhihong, Yan Maosheng, Li Zihuang, Yang Hongli, Zheng Tao, Li Gang, Li Xianming, Khan Muhammad
Department of Oncology, Shenzhen People's Hospital, The First Affiliated Hospital Of Southern University Of Science And Technology, Shenzhen, China.
Department of Radiation Oncology, Shenzhen People's Hospital, The Second College of Jinan University, Shenzhen, China.
Front Oncol. 2021 Oct 21;11:742971. doi: 10.3389/fonc.2021.742971. eCollection 2021.
Radiation therapy (RT) is the mainstay of brain metastases (BMs), and anti-PD-1 blockade has led to intracranial responses in non-small cell lung carcinoma (NSCLC) patients with BMs.
This study aimed to evaluate the efficacy and safety of adding anti-PD-1 blockade to RT in the management of NSCLC patients with BM in terms of survival outcome.
We retrospectively reviewed 70 NSCLC patients with BMs who were treated with whole brain radiation therapy (WBRT) between January 2016 and January 2021. Of the 70 patients, 29 additionally received anti-PD-1 therapy within 30 days of WBRT initiation. Baseline characteristics of the patients and efficacy outcomes such as progression-free survival (PFS) and overall survival (OS) were statistically compared using SPSS v26. Results were obtained using the Chi-square test/Fisher exact test, t-test, Kaplan-Meier, and Cox regression survival analyses.
The median survival for the entire cohort was 24 months (95% CI, 19.5-28.5). The median survival times for WBRT alone and WBRT plus anti-PD-1 therapy cohorts were 20 months (95% CI, 11.6-28.3) and 27 months (95% CI, 19.5-28.5), respectively (). There was no statistical difference in PFS for the treatment cohorts (median PFS for WBRT alone: 7 months . 12 months for WBRT plus anti-PD-1, ). In EGFR wild-type subgroup (n=31), both PFS () and OS () were significantly improved. Only the treatment group (WBRT plus anti-PD-1) was a significant predictor of OS on univariate and multivariate analyses (). There were no significant differences in adverse events among the treatment groups.
NSCLC patients with BM receiving additional anti-PD-1 therapy may derive better OS than WBRT alone without any increase in adverse events. Prospective well-designed studies are warranted to validate and elucidate the additive effects of the two modalities in this group of patients.
放射治疗(RT)是脑转移瘤(BMs)的主要治疗方法,抗程序性死亡蛋白1(PD-1)阻断疗法已使患有BMs的非小细胞肺癌(NSCLC)患者出现颅内反应。
本研究旨在从生存结局方面评估在接受RT治疗的NSCLC伴BM患者中加用抗PD-1阻断疗法的疗效和安全性。
我们回顾性分析了2016年1月至2021年1月期间接受全脑放射治疗(WBRT)的70例NSCLC伴BM患者。在这70例患者中,29例在WBRT开始后30天内额外接受了抗PD-1治疗。使用SPSS v26对患者的基线特征以及无进展生存期(PFS)和总生存期(OS)等疗效结局进行统计学比较。结果通过卡方检验/费舍尔精确检验、t检验、Kaplan-Meier法和Cox回归生存分析得出。
整个队列的中位生存期为24个月(95%置信区间,19.5 - 28.5)。单纯WBRT组和WBRT联合抗PD-1治疗组的中位生存时间分别为20个月(9t%置信区间,11.6 - 28.3)和27个月(95%置信区间,19.5 - 28.5)()。治疗组的PFS无统计学差异(单纯WBRT的中位PFS:7个月。WBRT联合抗PD-1为12个月,)。在表皮生长因子受体(EGFR)野生型亚组(n = 31)中,PFS()和OS()均显著改善。单因素和多因素分析显示,只有治疗组(WBRT联合抗PD-1)是OS的显著预测因素()。各治疗组之间不良事件无显著差异。
接受额外抗PD-1治疗的NSCLC伴BM患者可能比单纯接受WBRT有更好的OS,且不良事件无增加。需要进行前瞻性精心设计的研究来验证和阐明这两种治疗方式在该组患者中的附加效应。