Efficacy and safety of radiotherapy to delay second-line systemic therapy in patients with oligoprogressive hepatocellular carcinoma: study protocol of a multicentre, single-arm, phase II trial.

IF 4.3 2区 医学 Q2 ONCOLOGY
Therapeutic Advances in Medical Oncology Pub Date : 2025-04-23 eCollection Date: 2025-01-01 DOI:10.1177/17588359251334538
Haohua Wang, Xiang Zhang, Kunli Zhu, Shumei Jiang, Tianxing Liu, Rui Feng, Xue Dou, Lei Xu, Junyi He, Fang Shi, Jinbo Yue
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引用次数: 0

Abstract

Background: Hepatocellular carcinoma (HCC) is a highly aggressive cancer with a paucity of efficacious treatment options, particularly in advanced stages following first-line systemic therapy (FLST).

Objectives: The objective of this trial is to assess the efficacy and safety of radiotherapy as a treatment option to prolong progression-free survival (PFS) and delay the necessity for second-line systemic therapy (SLST) in patients with oligoprogressive HCC following FLST.

Design: Multicentre, single-arm, phase II trial.

Methods and analysis: This prospective, multicentre, single-arm phase II clinical trial will enrol 36 patients with oligoprogressive advanced HCC following FLST. A comprehensive clinical imaging evaluation will be conducted to confirm the presence of oligoprogressive disease, categorized as metachronous oligoprogression, repeat oligoprogression or induced oligoprogression. Furthermore, patients must have demonstrated stability of the primary HCC for a minimum of 3 months during FLST. Eligible patients will receive radiotherapy for all oligoprogressive lesions with a biologically effective dose (LQ, α/β = 10) of at least 60 Gy while continuing their current FLST until disease progression necessitates SLST. The primary endpoint is PFS, with secondary endpoints including objective remission rate, overall survival (OS), disease control rate, safety and duration of disease remission.

Ethics: The final protocol was approved by the Ethics Committee of the Affiliated Cancer Hospital of Shandong First Medical University.

Discussion: Given the greater number of options for FLST in advanced HCC, which have demonstrated improvements in PFS and OS, and the limited number and less effective SLST options, this phase II trial aims to evaluate the use of radiotherapy to extend PFS and delay the application of SLST in patients with oligoprogressive HCC after FLST. This approach may preserve SLST options for more aggressive, widespread metastatic disease in the future.

Trial registration: This study is registered on ClinicalTrials.gov identifier: NCT06261047.

放疗延迟低进展性肝癌患者二线全身治疗的有效性和安全性:一项多中心、单臂、II期试验的研究方案
背景:肝细胞癌(HCC)是一种高度侵袭性的癌症,缺乏有效的治疗选择,特别是在一线全身治疗(FLST)后的晚期。目的:本试验的目的是评估放疗作为一种治疗选择的有效性和安全性,以延长FLST后少进展性HCC患者的无进展生存期(PFS)和延迟二线全身治疗(SLST)的必要性。设计:多中心,单臂,II期试验。方法和分析:这项前瞻性、多中心、单臂II期临床试验将招募36例经FLST治疗的低进展期晚期HCC患者。将进行全面的临床影像学评估以确认是否存在寡进展性疾病,分类为异时性寡进展、重复寡进展或诱导寡进展。此外,患者必须在FLST期间证明原发性HCC的稳定性至少为3个月。符合条件的患者将接受至少60 Gy生物有效剂量(LQ, α/β = 10)的所有少进展病变的放疗,同时继续目前的FLST治疗,直到疾病进展需要SLST。主要终点是PFS,次要终点包括客观缓解率、总生存期(OS)、疾病控制率、安全性和疾病缓解持续时间。伦理:最终方案经山东第一医科大学附属肿瘤医院伦理委员会批准。讨论:考虑到晚期HCC中FLST的选择较多,已证明可以改善PFS和OS,而SLST的选择数量有限且效果较差,本II期试验旨在评估放疗在FLST后低进展性HCC患者中延长PFS和延迟SLST应用的应用。这种方法可以保留SLST的选择,在未来更积极的,广泛的转移性疾病。试验注册:本研究在ClinicalTrials.gov注册,注册编号:NCT06261047。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.20
自引率
2.00%
发文量
160
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Medical Oncology is an open access, peer-reviewed journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of cancer. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in medical oncology, providing a forum in print and online for publishing the highest quality articles in this area. This journal is a member of the Committee on Publication Ethics (COPE).
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