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Hepatic Arterial Infusion Chemotherapy Combined With PD-1 Inhibitors Plus Lenvatinib Versus PD-1 Inhibitors Plus Lenvatinib for Advanced Hepatocellular Carcinoma.
Mei, Jie; Tang, Yu-Hao; Wei, Wei; Shi, Ming; Zheng, Lie; Li, Shao-Hua; Guo, Rong-Ping.
Affiliation
  • Mei J; Department of Liver Surgery, Sun Yat-Sen University Cancer Center, Guangzhou, China.
  • Tang YH; State Key Laboratory of Oncology in South China, Guangzhou, China.
  • Wei W; Collaborative Innovation Center for Cancer Medicine, Guangzhou, China.
  • Shi M; Department of Liver Surgery, Sun Yat-Sen University Cancer Center, Guangzhou, China.
  • Zheng L; State Key Laboratory of Oncology in South China, Guangzhou, China.
  • Li SH; Collaborative Innovation Center for Cancer Medicine, Guangzhou, China.
  • Guo RP; Department of Liver Surgery, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Front Oncol ; 11: 618206, 2021.
Article in En | MEDLINE | ID: mdl-33718175
ABSTRACT

BACKGROUND:

Lenvatinib combined with programmed cell death protein-1 (PD-1) inhibitors has resulted in good survival outcomes in the treatment of unresectable hepatocellular carcinoma (HCC). Hepatic artery infusion chemotherapy (HAIC) has also attracted attention due to its high response rates and favorable survival for advanced HCC patients. The present study aimed to compare the efficacy of HAIC combined with PD-1 inhibitors plus lenvatinib (HPL) and PD-1 inhibitors plus lenvatinib (PL) in patients with advanced HCC.

METHODS:

Between July 2018 and December 2019, patients diagnosed with advanced HCC who initially received HPL or PL treatment were reviewed for eligibility. Efficacy was evaluated according to tumor response and survival.

RESULTS:

In total, 70 patients met the criteria and were included in the present study, and they were divided into the HPL group (n = 45) and PL group (n = 25). The overall response rate (40.0 vs. 16.0%, respectively; p = 0.038) and disease control rate (77.6 vs. 44.0%, respectively; p < 0.001) were higher in the HPL group than in the PL group. The median overall survival was 15.9 months in the HPL group and 8.6 months in the PL group (p = 0.0015; HR = 0.6; 95% CI 0.43-0.83). The median progression-free survival was 8.8 months in the HPL group and 5.4 months in the PL group (p = 0.0320; HR = 0.74; 95% CI 0.55-0.98).

CONCLUSION:

Compared to PL, HPL was associated with a significantly better treatment response and survival benefits for patients with advanced HCC.
Key words

Full text: 1 Database: MEDLINE Language: En Journal: Front Oncol Year: 2021 Type: Article Affiliation country: China

Full text: 1 Database: MEDLINE Language: En Journal: Front Oncol Year: 2021 Type: Article Affiliation country: China