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Transarterial chemoembolization plus a PD‐1 inhibitor with or without lenvatinib for intermediate‐stage hepatocellular carcinoma

伦瓦提尼 医学 肝细胞癌 内科学 不利影响 胃肠病学 实体瘤疗效评价标准 联合疗法 阶段(地层学) 肿瘤科 回顾性队列研究 索拉非尼 进行性疾病 化疗 生物 古生物学
作者
Yan‐Jun Xiang,Li Wang,Hongming Yu,Xiaowei Li,Yuqiang Cheng,Weijun Wang,Jin‐Kai Feng,Meng‐Han Bo,Yingyi Qin,Yitao Zheng,Yunfeng Shan,Liping Zhou,Jian Zhai,Shuqun Cheng
出处
期刊:Hepatology Research [Wiley]
卷期号:52 (8): 721-729 被引量:29
标识
DOI:10.1111/hepr.13773
摘要

Abstract Aim Transarterial chemoembolization (TACE) combined with a PD‐1 inhibitor and TACE combined with a PD‐1 inhibitor and lenvatinib have recently been reported as promising treatments to improve the prognosis of hepatocellular carcinoma (HCC) patients. This study aims to compare the efficacy of these two treatments. Methods A retrospective study was conducted, and patients were recruited from two centers in China. Progression‐free survival (PFS) and overall survival (OS) were compared, and the objective response rate (ORR) and disease control rate (DCR) were evaluated according to the modified Response Evaluation Criteria in Solid Tumors (mRECIST). Treatment‐related adverse events (AEs) were analyzed to assess safety. Results The median follow‐up for the entire cohort was 11.4 months. Of the 103 patients included in this study, 56 received triple therapy, and 47 received doublet therapy. PFS was significantly higher in the triple therapy group than in the doublet therapy group (mPFS 22.5 vs. 14.0 months, P < 0.001). Similar results were obtained in terms of OS ( P = 0.001). The ORR and DCR were also better in the triple therapy group (64.3% vs. 38.3%, P = 0.010; 85.7% vs. 57.4%, P = 0.002). The most common AEs in the triple therapy group were decreased albumin (55.3%), decreased platelet count (51.8%) and hypertension (44.6%). Conclusions The combination of TACE with a PD‐1 inhibitor and lenvatinib in patients with BCLC stage B HCC might result in significantly improved clinical outcomes with a manageable safety profile compared with TACE with a PD‐1 inhibitor.
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