The effect of switch therapy to tenofovir versus entecavir maintenance on recurrence of hepatocellular carcinoma after surgery (SWITE): study protocol for a randomized controlled trial

被引:0
作者
Peng, Wei [1 ,2 ]
Yi, Mengshi [3 ]
Qi, Xin [4 ]
Qi, Weili [1 ]
Li, Chuan [1 ]
Wen, Tianfu [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Gen Surg, Div Liver Surg, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Chinese Evidence Based Med Ctr, Chengdu, Peoples R China
[3] Army Med Univ, Affiliated Hosp 1, Dept Hepatobiliary Surg, Chongqing, Peoples R China
[4] Sichuan Univ, West China Sch Med, Chengdu, Peoples R China
基金
中国国家自然科学基金;
关键词
Antiviral therapy; Entecavir; Hepatocellular carcinoma; Recurrence; Tenofovir disoproxil fumarate; HEPATITIS-B PATIENTS; ANALOGS; NUCLEOSIDE; SUPPRESSION; RESECTION; PATTERNS; RISK;
D O I
10.1186/s13063-023-07822-y
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
BackgroundAntiviral therapy has been reported to be associated with lower recurrence rate of hepatocellular carcinoma (HCC) for patients with hepatitis B virus (HBV) infection. While entecavir (ETV) and tenofovir disoproxil fumarate (TDF) were both recommended as first-line therapies for HBV patients, recent retrospective studies proposed a lower incidence rate of HCC occurrence or recurrence in those receiving TDF compared ETV. However, the survival benefits of switching to TDF therapy after prolonged ETV treatment before surgery remain uncertain. We delineate the rationale and design of SWITE, a randomized, open-label, phase III trial contrasting TDF switch therapy versus ETV maintenance in HBV-related HCC patients.Methods and analysisThis is a prospective, randomized, controlled, single-center study with two parallel groups of patients with HBV-related HCC who have received long-term ETV therapy before surgery. West China Hospital will enroll 238 patients, randomized in a 1:1 ratio to TDF switch therapy or ETV maintenance after surgery. The primary endpoint of this study is 3-year recurrence free survival (RFS), with the secondary endpoint being 3-year overall survival (OS) after curative surgery of HCC. Safety events will be diligently recorded.Ethics and disseminationThe study protocol aligns with the ethical guidelines of the 1975 Declaration of Helsinki. It was approved by ethics committee of West China Hospital (approval number: 2022-074) and was registered with chictr.org.cn (chiCTR2200057867). Informed consent will be obtained from all participants. The results of this trial will be published in peer-reviewed journals and presentations at national and international conferences relevant to this topic.Trial registrationchiCTR2200057867. Date of registration is March 20 2022.
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