Efficacy and safety of subsequent radiotherapy in patients with advanced-stage hepatocellular carcinoma treated with immune checkpoint inhibitors

被引:1
|
作者
Ning, Cong [1 ]
Jia, Jun [2 ]
Zhang, Xinmu [1 ]
Sun, Jing [2 ]
Wang, Yunchao [1 ]
Xue, Jingnan [1 ]
Zhang, Longhao [1 ]
Hou, Xiaorong [3 ]
Yang, Xiaobo [1 ]
Sang, Xinting [1 ]
Duan, Xuezhang [2 ]
Zhao, Haitao [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll CAMS, Peking Union Med Coll Hosp, Dept Liver Surg, State Key Lab Complex Severe & Rare Dis, 1 Shuai Fu Yuan, Beijing 100730, Peoples R China
[2] Peoples Liberat Army PLA Gen Hosp, Chinese PLA Med Sch, Dept Radiotherapy, Sr Dept Oncol,Med Ctr 5, 100 Xi Si Huan Middle Rd, Beijing 100039, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll CAMS, Peking Union Med Coll Hosp, Dept Radiat Oncol, Beijing, Peoples R China
关键词
Subsequent radiotherapy; immunotherapy; immune checkpoint inhibitors (ICIs); disease status; advanced-stage hepatocellular carcinoma; TRANSARTERIAL CHEMOEMBOLIZATION; THERAPY; CANCER; CABOZANTINIB; IPILIMUMAB; NIVOLUMAB; TRIAL;
D O I
10.21037/hbsn-23-134
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: This study aimed to evaluate the efficacy and safety of subsequent radiotherapy (RT) for patients with advanced-stage hepatocellular carcinoma (HCC) who had lesion enlargement or new lesions (NLs) during immune checkpoint inhibitor (ICI) therapy. Methods: 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.Results: 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. Conclusions: 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.
引用
收藏
页码:882 / 898
页数:17
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