Ning Cong, Jia Jun, Zhang Xinmu, Sun Jing, Wang Yunchao, Xue Jingnan, Zhang Longhao, Hou Xiaorong, Yang Xiaobo, Sang Xinting, Duan Xuezhang, Zhao Haitao
Department of Liver Surgery, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College (CAMS & PUMC), Beijing, China.
Department of Radiotherapy, Senior Department of Oncology, The Fifth Medical Center of People's Liberation Army (PLA) General Hospital, Chinese PLA Medical School, Beijing, China.
Hepatobiliary Surg Nutr. 2023 Dec 1;12(6):882-897. doi: 10.21037/hbsn-23-134. Epub 2023 May 31.
The development of immunotherapy resistance is associated with a poor prognosis in patients diagnosed with hepatocellular carcinoma (HCC) who are undergoing treatment with immune checkpoint inhibitors (ICI). This study aimed to evaluate the efficacy and safety of subsequent radiotherapy (RT) for patients with advanced-stage HCC who had lesion enlargement or new lesions (NLs) during ICI therapy.
This retrospective observational study enrolled 36 patients with advanced-stage HCC who underwent subsequent RT for lesion enlargement or NLs during ICI therapy from two centers. The primary endpoints were progression-free survival (PFS) and overall survival (OS). The secondary endpoints included objective response rate (ORR), disease control rate (DCR), 1- and 2-year local control (LC) rates, in-field PFS (IFPFS), out-field PFS (OFPFS), and safety.
The median follow-up time was 15.3 months. The median PFS was 7.4 months [95% confidence interval (CI): 3.1-11.7 months], and the median OS was 18.8 months (95% CI: 17.1-20.5 months). ORR and DCR were 38.9% and 72.2%, respectively. In addition, the median IFPFS was 17.8 months (95% CI: 11.5-24.2 months), median OFPFS was 7.9 months (95% CI: 3.4-12.5 months), and estimated 1- and 2-year LC rates were 67.1% and 31.9%, respectively. The most common treatment-related adverse events (all grades) were diarrhea (33.3%), rash (30.6%), and malaise (27.8%); a total of 14 (38.9%) patients developed grade 3-4 AEs.
Subsequent RT showed reliable antitumor effects and an acceptable safety profile in patients with advanced-stage HCC who had unsatisfactory response to ICI therapy; therefore, it could serve as an optional salvage strategy.
免疫治疗耐药的发生与接受免疫检查点抑制剂(ICI)治疗的肝细胞癌(HCC)患者的不良预后相关。本研究旨在评估后续放疗(RT)对在ICI治疗期间出现病灶增大或新病灶(NLs)的晚期HCC患者的疗效和安全性。
这项回顾性观察性研究纳入了36例晚期HCC患者,这些患者来自两个中心,在ICI治疗期间因病灶增大或NLs接受了后续RT。主要终点为无进展生存期(PFS)和总生存期(OS)。次要终点包括客观缓解率(ORR)、疾病控制率(DCR)、1年和2年局部控制(LC)率、靶区内PFS(IFPFS)、靶区外PFS(OFPFS)和安全性。
中位随访时间为15.3个月。中位PFS为7.4个月[95%置信区间(CI):3.1 - 11.7个月],中位OS为18.8个月(95%CI:17.1 - 20.5个月)。ORR和DCR分别为38.9%和72.2%。此外,中位IFPFS为17.8个月(95%CI:11.5 - 24.2个月),中位OFPFS为7.9个月(95%CI:3.4 - 12.5个月),估计1年和2年LC率分别为67.1%和31.9%。最常见的治疗相关不良事件(所有级别)为腹泻(33.3%)、皮疹(30.6%)和不适(27.8%);共有14例(38.9%)患者发生3 - 4级不良事件。
对于对ICI治疗反应不佳的晚期HCC患者,后续RT显示出可靠的抗肿瘤效果和可接受的安全性;因此,它可作为一种可选的挽救策略。