Neoadjuvant therapy of sequential TACE, camrelizumab, and apatinib for single huge hepatocellular carcinoma (NEO-START): study protocol for a randomized controlled trial

被引:7
作者
Hao, Yun [1 ]
Xie, Fei [2 ]
Zhou, Yongjie [3 ]
Li, Chuan [1 ]
Zhang, Xiaoyun [1 ]
Shen, Junyi [1 ]
Yao, Minghong [4 ]
Sun, Xin [4 ]
Zhou, Jin [1 ]
Wen, Tianfu [1 ]
Peng, Wei [1 ,4 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Gen Surg, Div Liver Surg, Chengdu, Peoples R China
[2] First Peoples Hosp Neijiang, Dept Hepat Biliary Pancreat Surg, Neijiang, Peoples R China
[3] Sichuan Univ, West China Hosp, Lab Liver Transplantat, Key Lab Transplant Engn & Immunol,NHC, Chengdu, Peoples R China
[4] Sichuan Univ, West China Hosp, Chinese Evidence based Med Ctr, Chengdu, Peoples R China
关键词
Hepatocellular carcinoma; Neoadjuvant therapy; Camrelizumab; Apatinib; Transarterial chemoembolization; PREOPERATIVE TRANSARTERIAL CHEMOEMBOLIZATION; RESECTION; SURGERY; CM;
D O I
10.1186/s13063-024-08340-1
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundThe high recurrence rate after liver resection emphasizes the urgent need for neoadjuvant therapy in hepatocellular carcinoma (HCC) to enhance the overall prognosis for patients. Immune checkpoint inhibitors, camrelizumab combined with an anti-angiogenic tyrosine kinase inhibitor (TKI) apatinib, have emerged as a first-line treatment option for patients with unresectable HCC, yet its neoadjuvant application in combination with transarterial chemoembolization (TACE) in HCC remains unexplored. Therefore, this study aims to investigate the efficacy and safety of sequential TACE, camrelizumab, and apatinib as a neoadjuvant therapy for single, huge HCC.MethodsThis multi-center, open-label randomized phase 3 trial will be conducted at 7 tertiary hospitals. Patients with single huge (>= 10 cm in diameter), resectable HCC will be randomly assigned in a 1:1 ratio to arm of surgery alone or arm of neoadjuvant therapy followed by surgery. In the neoadjuvant therapy group, patients will receive TACE within 1 week after randomization, followed by camrelizumab (200 mg q2w, 4 cycles), along with apatinib (250 mg qd, 2 months). Patients will receive liver resection after neoadjuvant therapy unless the disease is assessed as progressive. The primary outcome is recurrence-free survival (RFS) at 1 year. The planned sample size of 60 patients will be calculated to permit the accumulation of sufficient RFS events in 1 year to achieve 80% power for the RFS primary endpoint.DiscussionSynergistic effects provided by multimodality therapy of locoregional treatment, TKI, and anti-programmed cell death 1 inhibitor significantly improved overall survival for patients with unresectable HCC. Our trial will investigate the efficacy and safety of the triple combination of TACE, camrelizumab, and apatinib as a neoadjuvant strategy for huge, resectable HCC.Trial registrationwww.chitr.org.cn ChiCTR2300078086. Registered on November 28, 2023. Start recruitment: 1st January 2024. Expected completion of recruitment: 15th June 2025.
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