Ursino Moreno, Villacampa Guillermo, Rekowski Jan, Dimairo Munyaradzi, Solovyeva Olga, Ashby Deborah, Berlin Jordan, Boix Oliver, Calvert Melanie, Chan An-Wen, Coschi Courtney H, Evans Thomas R Jeffry, Garrett-Mayer Elizabeth, Golub Robert M, Guo Christina, Hayward Kathryn S, Hopewell Sally, Isaacs John D, Ivy S Percy, Jaki Thomas, Kholmanskikh Olga, Kightley Andrew, Lee Shing, Liu Rong, Mander Adrian, Marshall Lynley V, Matcham James, Patel Dhrusti, Peck Richard, Rantell Khadija Rerhou, Richards Dawn P, Rouhifard Mahtab, Seymour Lesley, Tanaka Yoshiya, Weir Christopher J, de Bono Johann, Yap Christina
ReCAP/F CRIN, INSERM, 5400, Nancy, France.
Unit of Clinical Epidemiology, University Hospital Centre Robert Debré, Université Paris Cité, Paris, France.
EClinicalMedicine. 2025 Jan 10;79:102988. doi: 10.1016/j.eclinm.2024.102988. eCollection 2025 Jan.
Transparent and accurate reporting in early phase dose-finding (EPDF) clinical trials is crucial for informing subsequent larger trials. The SPIRIT statement, designed for trial protocol content, does not adequately cover the distinctive features of EPDF trials. Recent findings indicate that the protocol contents in past EPDF trials frequently lacked completeness and clarity. To address this gap, the international consensus-driven SPIRIT-DEFINE checklist was developed through a robust methodological framework for guideline development, with the aim to improve completeness and clarity in EPDF trial protocols. The checklist builds on the SPIRIT statement, adding 17 new items and modifying 15 existing ones.The SPIRIT-DEFINE explanation and elaboration (E&E) document provides comprehensive information to enhance understanding and usability of the SPIRIT-DEFINE checklist when writing an EPDF trial protocol. Each new or modified checklist item is accompanied by a detailed description, its rationale with supportive evidence, and examples of good reporting curated from EPDF trial protocols covering a range of therapeutic areas and interventions. We recommend utilising this paper alongside the SPIRIT statement, and any relevant extensions, to enhance the development and review of EPDF trial protocols.By facilitating adoption of the SPIRIT-DEFINE statement for EPDF trials, this E&E document can promote enhancement of methodological rigour, patient safety, transparency, and facilitate the generation of high-quality, reproducible evidence that will strengthen the foundation of early phase research and ultimately improve patient outcomes.
This work is a further extension of the SPIRIT-DEFINE study, which obtained no external funding. The principal investigator (CY) used internal staff resources, together with additional resources from external partners, to conduct this study. The SPIRIT-DEFINE study is a component of the DEFINE project, which also developed the MRC/NIHR funded CONSORT-DEFINE guidance. ICR-CTSU receives programmatic infrastructure funding from Cancer Research UK (C1491/A25351; CTUQQR-Dec22/100004), which has contributed to accelerating the advancement and successful completion of this work.
在早期剂量探索(EPDF)临床试验中进行透明且准确的报告对于为后续更大规模的试验提供信息至关重要。专为试验方案内容设计的《标准方案条目与报告规范(SPIRIT)声明》并未充分涵盖EPDF试验的独特特征。最近的研究结果表明,过去EPDF试验中的方案内容常常缺乏完整性和清晰度。为弥补这一差距,通过一个稳健的指南制定方法框架,制定了由国际共识驱动的《SPIRIT-DEFINE清单》,旨在提高EPDF试验方案的完整性和清晰度。该清单以《SPIRIT声明》为基础,新增了17项内容并修改了15项现有内容。《SPIRIT-DEFINE解释与阐述(E&E)文件》提供了全面信息,以增强在撰写EPDF试验方案时对《SPIRIT-DEFINE清单》的理解和实用性。清单中的每一项新增或修改内容都附有详细描述、其依据及支持证据,以及从涵盖一系列治疗领域和干预措施的EPDF试验方案中精选出的良好报告示例。我们建议将本文与《SPIRIT声明》及任何相关扩展内容一起使用,以加强EPDF试验方案的制定和审查。通过促进在EPDF试验中采用《SPIRIT-DEFINE声明》,本E&E文件可推动提高方法学严谨性、患者安全性和透明度,并有助于生成高质量、可重复的证据,从而加强早期研究的基础并最终改善患者结局。
本工作是《SPIRIT-DEFINE研究》的进一步扩展,该研究未获得外部资金。首席研究员(CY)使用内部员工资源以及外部合作伙伴提供的额外资源开展本研究。《SPIRIT-DEFINE研究》是DEFINE项目的一个组成部分,该项目还制定了由医学研究理事会/英国国家健康研究所资助的《CONSORT-DEFINE指南》。英国癌症研究中心(C1491/A25351;CTUQQR-Dec22/100004)为ICR-CTSU提供了项目基础设施资金,这有助于加速这项工作的推进和圆满完成。