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REFRACT试验:贝叶斯功效先验在随机、序贯II期适应性平台试验中的应用

The REFRACT trial: implementation of Bayesian power priors in a randomised, sequential phase II adaptive platform trial.

作者信息

Gaskell Charlotte, Linton Kim, Bishton Mark, McIlroy Graham, Lax Siân, Fox Sonia, Hopkins Louise, Collings Rebecca, Rhodes Malcolm, Seale Tania, Jackson Aimee

机构信息

Cancer Research UK Clinical Trials Unit, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.

Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester, M20 4BX, UK.

出版信息

BMC Med Res Methodol. 2025 May 3;25(1):121. doi: 10.1186/s12874-025-02575-5.

Abstract

BACKGROUND

REFRACT is a randomised trial aimed at rapidly evaluating multiple novel therapies against standard treatment for relapsed or refractory follicular lymphoma (rrFL) using a minimal number of patients. To this end, we designed a prospective, adaptive, sequentially randomised clinical trial to allow multiple novel therapies to be assessed sequentially against a control arm of investigator choice standard therapy (ICT).

METHODS

REFRACT uses a Bayesian power priors approach enabling the sharing of control arm data from previous treatment rounds. The design allows for the randomisation ratio to be changed and fixed to 1:4 in later treatment rounds resulting in fewer patients being recruited to the control arm.

RESULTS

Following extensive simulations, we arrived at the selected design of three sequential treatment rounds, each with a control group and a novel experimental arm assessed for the primary outcome of complete metabolic response (CMR) at 24 weeks. Patients in Round 1 are randomised using a 1:1 allocation, with Rounds 2 and 3 randomised using a 1:4 allocation, in favour of experimental treatment. Using Bayesian power priors, data from control patients in earlier rounds will be shared to improve the operating characteristics in the current round. Previous control arm patients will be weighted at 75% of an active control patient within the prior, with opportunities for adjustment should control treatments change over time.

CONCLUSIONS

With the use of power priors and an adaptive design this trial will sequentially evaluate three novel treatment regimens in a disease that urgently requires additional treatment options. REFRACT opened to recruitment in July 2023.

TRIAL REGISTRATION

EudraCT: 2022-000677-75; 10-Feb-2022.

CLINICALTRIALS

gov: NCT05848765; 08-May-2023.

摘要

背景

REFRACT是一项随机试验,旨在使用最少数量的患者快速评估针对复发或难治性滤泡性淋巴瘤(rrFL)的多种新型疗法与标准治疗的疗效对比。为此,我们设计了一项前瞻性、适应性、序贯随机临床试验,以便针对研究者选择的标准治疗(ICT)的对照组,依次评估多种新型疗法。

方法

REFRACT采用贝叶斯功率先验方法,能够共享来自先前治疗轮次的对照组数据。该设计允许改变随机化比例,并在后续治疗轮次中将其固定为1:4,从而减少招募到对照组的患者数量。

结果

经过广泛模拟,我们确定了三阶段序贯治疗的设计方案,每个阶段都有一个对照组和一个新型试验组,评估24周时完全代谢缓解(CMR)的主要结局。第1轮患者按1:1分配进行随机分组,第2轮和第3轮按1:4分配进行随机分组,更有利于试验性治疗。使用贝叶斯功率先验,早期轮次对照组患者的数据将被共享,以改善本轮的操作特性。先前对照组患者在先前数据中的权重为活性对照患者的75%,如果对照治疗随时间变化,将有调整的机会。

结论

通过使用功率先验和适应性设计,该试验将在急需更多治疗选择的疾病中依次评估三种新型治疗方案。REFRACT于2023年7月开始招募患者。

试验注册

欧洲药品管理局临床试验数据库(EudraCT):2022-000677-75;2022年2月10日。

美国国立医学图书馆临床试验注册库(ClinicalTrials.gov):NCT05848765;2023年5月8日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/470f/12049029/e4ab1f876bc7/12874_2025_2575_Fig1_HTML.jpg

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