Patients with hepatocellular carcinoma extrahepatic metastases can benefit from hepatic arterial infusion chemotherapy combined with lenvatinib plus programmed death-1 inhibitors

被引:11
作者
Guan, Renguo [1 ,2 ,3 ]
Zhang, Nan [8 ]
Deng, Min [6 ]
Lin, Ye [4 ]
Huang, Guanjie [7 ]
Fu, Yizhen [1 ,2 ,3 ]
Zheng, Zehao [1 ,2 ,3 ]
Wei, Wei [1 ,2 ,3 ]
Zhong, Chong [5 ]
Zhao, Haitao [8 ]
Mei, Jie [1 ,2 ,3 ]
Guo, Rongping [1 ,2 ,3 ]
机构
[1] Sun Yat Sen Univ, Canc Ctr, Dept Liver Surg, 651 Dongfeng East Rd, Guangzhou 510060, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Guangzhou, Peoples R China
[3] Sun Yat sen Univ, Guangdong Prov Clin Res Ctr Canc, Guangzhou, Peoples R China
[4] Southern Med Univ, Guangdong Prov Peoples Hosp, Guangdong Acad Med Sci, Dept Gen Surg, Ganzhou, Peoples R China
[5] Guangzhou Univ Chinese Med, Dept Hepatobiliary Surg, Affiliated Hosp 1, 16,Baiyun Airport Rd, Guangzhou 510450, Guangdong, Peoples R China
[6] Sun Yat Sen Univ, Affiliated Hosp 7, Dept Gen Surg, Shenzhen, Peoples R China
[7] Maoming Peoples Hosp, Dept Oncol, Maoming, Guangdong, Peoples R China
[8] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Liver Surg, 1 Shuaifuyuan, Beijing 100730, Peoples R China
基金
中国国家自然科学基金;
关键词
extrahepatic metastases; hepatic arterial infusion chemotherapy; hepatocellular carcinoma; lenvatinib; PD-1; inhibitors; prognosis; EFFICACY; SAFETY; BEVACIZUMAB; GUIDELINES;
D O I
10.1097/JS9.0000000000001378
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Lenvatinib plus programmed death-1 (PD-1) inhibitors (LEN-P) have been recommended in China for patients with advanced hepatocellular carcinoma (HCC). However, they provide limited survival benefits to patients with extrahepatic metastases. We aimed to investigate whether combining hepatic arterial infusion chemotherapy (HAIC) with LEN-P could improve its efficacy. Materials and methods: This multicenter cohort study included patients with HCC extrahepatic metastases who received HAIC combined with LEN-P (HAIC-LEN-P group, n=127) or LEN-P alone (n=103) as the primary systemic treatment between January 2019 and December 2022. Baseline data were balanced using a one-to-one propensity score matching (PSM) and inverse probability of treatment weighting (IPTW). Results: After PSM, the HAIC-LEN-P group significantly extended the median overall survival (mOS) and median progression-free survival (mPFS), compared with the LEN-P group (mOS: 27.0 months vs. 9.0 months, P<0.001; mPFS: 8.0 months vs. 3.0 months, P=0.001). After IPTW, the mOS [hazard ratio (HR)=0.384, P<0.001] and mPFS (HR=0.507, P<0.001) were significantly higher in the HAIC-LEN-P group than in the LEN-P group. The HAIC-LEN-P group's objective response rate was twice as high as that of the LEN-P group (PSM cohort: 67.3% vs. 29.1%, P<0.001; IPTW cohort: 66.1% vs. 27.8%, P<0.001). Moreover, the HAIC-LEN-P group exhibited no noticeable increase in the percentages of grade 3 and 4 adverse events compared with the LEN-P group (P>0.05). Conclusion: HAIC can improve the efficacy of LEN-P in patients with HCC extrahepatic metastases and may be an alternative treatment for advanced HCC management.
引用
收藏
页码:4062 / 4073
页数:12
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