TACE plus lenvatinib and tislelizumab for intermediate-stage hepatocellular carcinoma beyond up-to-11 criteria: a multicenter cohort study

被引:2
|
作者
Chen, Song [1 ]
Tang, Shuangyan [2 ]
Shi, Feng [3 ]
Cai, Hongjie [2 ]
Wu, Zhiqiang [2 ]
Wang, Liguang [4 ]
Ma, Ping [5 ]
Zhou, Yuanmin [6 ]
Mai, Qicong [3 ]
Wang, Fan [2 ]
Lai, Jiaming [6 ]
Chen, Xiaoming [3 ]
Chen, Huanwei [4 ]
Guo, Wenbo [2 ]
机构
[1] Sun Yat Sen Univ Canc Ctr, Guangdong Prov Clin Res Ctr Canc, Dept Minimally Invas Intervent Therapy, State Key Lab Oncol South China, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Intervent Radiol, Guangzhou, Peoples R China
[3] Guangdong Prov Peoples Hosp, Dept Intervent Radiol, Guangzhou, Peoples R China
[4] First Peoples Hosp Foshan, Dept Hepatopancreat Surg, Foshan, Peoples R China
[5] Twelfth Peoples Hosp Guangzhou, Dept Oncol, Guangzhou, Peoples R China
[6] Sun Yat Sen Univ, Affiliated Hosp 1, Ctr Hepatopancreatobiliary Surg, Guangzhou, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
基金
中国国家自然科学基金;
关键词
hepatocellular carcinoma; intermediate-stage; up-to-eleven criteria; transartrial chemoembolization; combination therapy; TRANSARTERIAL CHEMOEMBOLIZATION; 1ST-LINE TREATMENT; SUBSTAGING SYSTEM; DOUBLE-BLIND; BCLC STAGE; SORAFENIB; SUBCLASSIFICATION; BEVACIZUMAB; VALIDATION; MANAGEMENT;
D O I
10.3389/fimmu.2024.1430571
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Intermediate-stage (BCLC-B) hepatocellular carcinoma (HCC) beyond the up-to-11 criteria represent a significant therapeutic challenge due to high and heterogeneous tumor burden. This study evaluated the effectiveness and safety of transarterial chemoembolization (TACE) in combination with lenvatinib and tislelizumab for these patients. Methods In this retrospective cohort study, patients with unresectable intermediate-stage HCC beyond the up-to-11 criteria were enrolled and divided into TACE monotherapy (T), TACE combined with lenvatinib (TL), or TACE plus lenvatinib and tislelizumab (TLT) group based on the first-line treatment, respectively. The primary endpoint was overall survival (OS). The secondary outcomes included progression-free survival (PFS), tumor response according to RESIST1.1 and modified RECIST, and adverse events (AEs). Results There were 38, 45, and 66 patients in the T, TL, and TLT groups, respectively. The TLT group exhibited significantly higher ORR and DCR than the other two groups, as assessed by either mRECIST or RECIST 1.1 (all P<0.05). Median PFS and OS were significantly longer in the TLT group compared with the T group (PFS: 8.5 vs. 4.4 months; OS: 31.5 vs. 18.5 months; all P<0.001) and TL group (PFS: 8.5 vs. 5.5 months; OS: 31.5 vs. 20.5 months; all P<0.05). The incidence of TRAEs was slightly higher in the TLT and TL groups than in the T group, while all the toxicities were tolerable. No treatment-related death occurred in all groups. Conclusions TACE combined with lenvatinib and tislelizumab significantly improved the survival benefit compared with TACE monotherapy and TACE plus lenvatinib in patients with intermediate-stage HCC beyond the up-to-11 criteria, with an acceptable safety profile.
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页数:11
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