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Hepatic arterial infusion chemotherapy plus camrelizumab and apatinib for advanced hepatocellular carcinoma.
Zuo, Mengxuan; Cao, Yuzhe; Yang, Yi; Zheng, Guanglei; Li, Da; Shao, Hongyan; Ma, Qiaoyun; Song, Peng; An, Chao; Li, Wang.
Afiliação
  • Zuo M; Department of Minimally Invasive Interventional Therapy, Sun Yat-Sen University Cancer Center, 651 Dongfeng East Road, Guangzhou, 510060, People's Republic of China.
  • Cao Y; State Key Laboratory of Oncology in South China, Guangzhou, People's Republic of China.
  • Yang Y; Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, People's Republic of China.
  • Zheng G; Department of Minimally Invasive Interventional Therapy, Sun Yat-Sen University Cancer Center, 651 Dongfeng East Road, Guangzhou, 510060, People's Republic of China.
  • Li D; State Key Laboratory of Oncology in South China, Guangzhou, People's Republic of China.
  • Shao H; Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, People's Republic of China.
  • Ma Q; Department of Hepatobiliary Surgery, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
  • Song P; Department of Minimally Invasive Interventional Therapy, Sun Yat-Sen University Cancer Center, 651 Dongfeng East Road, Guangzhou, 510060, People's Republic of China.
  • An C; State Key Laboratory of Oncology in South China, Guangzhou, People's Republic of China.
  • Li W; Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, People's Republic of China.
Hepatol Int ; 2024 Jul 03.
Article em En | MEDLINE | ID: mdl-38961006
ABSTRACT
BACKGROUND AND

AIMS:

There is limited information on combination of hepatic arterial infusion chemotherapy (HAIC) and systemic therapy for advanced hepatocellular carcinoma (Ad-HCC). We aim to compare the efficacy and safety of HAIC plus camrelizumab (a PD-1 inhibitor) and apatinib (an VEGFR-2 inhibitor) versus camrelizumab and apatinib for Ad-HCC.

METHODS:

From April 2019 to October 2022, 416 patients with Ad-HCC who received either HAIC plus camrelizumab and apatinib (TRIPLET protocol, n = 207) or camrelizumab and apatinib (C-A protocol, n = 209) were reviewed retrospectively. The propensity score matching (PSM) was used to reduce selective bias. Overall survival (OS) and progression-free survival (PFS) were compared using the Kaplan-Meier method with the log-rank test. Cox regression analyses of independent prognostic factors were evaluated.

RESULTS:

After PSM 11, 109 patients were assigned to two groups. The median OS of not reached in the TRIPLET group was significantly longer than that of 19.9 months in the C-A group (p < 0.001), while in the TRIPLET group, the median PFS of 11.5 months was significantly longer than that of 9.6 months in the C-A group (p < 0.001). Multivariate analyses showed that the factors significantly affected the OS were CTP grade, tumor number > 3, and TRIPLET treatment (p < 0.001). Grade 3/4 adverse events occurred at a rate of 82.1% vs. 71.3% in TRIPLET and C-A groups, respectively.

CONCLUSION:

The TRIPLET protocol has promising survival benefits in the management of patients with Ad-HCC, with acceptable safety. TRAIL REGISTRATION The study has been retrospectively registered at Chinese Clinical Trial Registry ( https//www.chictr.org.cn/ , ChiCTR2300075828).
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Hepatol Int Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Hepatol Int Ano de publicação: 2024 Tipo de documento: Article