医学
阿替唑单抗
肝细胞癌
贝伐单抗
内科学
肿瘤科
不利影响
无进展生存期
放射治疗
中性粒细胞减少症
全身疗法
化疗
放射科
癌症
乳腺癌
无容量
免疫疗法
作者
Kang Wang,Yan‐Jun Xiang,Hongming Yu,Yuqiang Cheng,Zong‐Han Liu,Jing-Ya Zhong,Shuang Feng,Qian‐Zhi Ni,Hongfei Zhu,Weiwei Pan,Jingjing Li,Chao Liang,Hongkun Zhou,Yan Meng,Wan Yee Lau,Shuqun Cheng
标识
DOI:10.3389/fimmu.2023.1107542
摘要
Background and aims The efficacy and safety of systemic atezolizumab and bevacizumab (atezo/bev) in treatment of patients with unresectable hepatocellular carcinoma (HCC) have been demonstrated. However, the efficacy of this treatment in patients with HCC and extrahepatic portal vein tumor thrombus (ePVTT) is not satisfactory. This study aimed to study the efficacy and safety of combining intensity-modulated radiotherapy (IMRT) with systemic atezo/bev in treatment of these patients. Methods This multicenter prospective study included patients with ePVTT treated with IMRT combined with atezo/bev from March to September 2021 in three centers in China. The outcomes of this study included objective response rate (ORR), overall survival (OS), progression-free survival (PFS), time to progression (TTP), and association between response and tumor mutational burden (TMB). Treatment-related adverse events (TRAEs) were analyzed to assess safety. Results Of 30 patients in this study, the median follow-up was 7.4 months. Based on the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1, the ORR was 76.6%, the median OS for the entire cohort was 9.8 months, the median PFS was 8.0 months, and the median TTP was not reached. This study failed to establish a significant correlation between TMB with any of the following outcomes, including ORR, OS, PFS or TTP. The most common TRAEs at all levels were neutropenia (46.7%), and the most common grade 3/4 TRAE was hypertension (16.7%). There was no treatment-related deaths. Conclusions IMRT combined with atezo/bev showed encouraging treatment efficacy with an acceptable safety profile, making this treatment to be a promising option for HCC patients with ePVTT. Further studies are required to support the findings of this preliminary study. Clinical trial registration http://www.chictr.org.cn , Identifier ChiCTR2200061793.
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