利用分布式学习开发和验证肛门癌预后模型:国际多中心 atomCAT2 研究协议。

Stelios Theophanous, Per-Ivar Lønne, Ananya Choudhury, Maaike Berbee, Andre Dekker, Kristopher Dennis, Alice Dewdney, Maria Antonietta Gambacorta, Alexandra Gilbert, Marianne Grønlie Guren, Lois Holloway, Rashmi Jadon, Rohit Kochhar, Ahmed Allam Mohamed, Rebecca Muirhead, Oriol Parés, Lukasz Raszewski, Rajarshi Roy, Andrew Scarsbrook, David Sebag-Montefiore, Emiliano Spezi, Karen-Lise Garm Spindler, Baukelien van Triest, Vassilios Vassiliou, Eirik Malinen, Leonard Wee, Ane L Appelt
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引用次数: 0

摘要

背景:肛门癌是一种罕见的癌症,发病率呈上升趋势。尽管最先进的放化疗取得了相对较好的疗效,但进一步提高疾病控制率和降低毒性仍具有挑战性。利用常规收集的数据开发和验证预后模型可为治疗方法的开发和选择提供新的见解。然而,由于癌症的罕见性,很难获得足够的数据(尤其是来自单个中心的数据)来开发和验证可靠的模型。此外,多中心模型开发还受到伦理障碍和数据保护法规的阻碍,这些往往限制了患者数据的获取。分布式(或联盟式)学习允许使用来自多个中心的数据开发模型,而无需将任何个人层面的患者数据离开原中心,从而保护了患者数据隐私。这项工作建立在三中心 atomCAT1 概念验证研究的基础上,并介绍了多中心 atomCAT2 研究的方案,该研究旨在为化疗放疗后肛门癌的三种临床重要结果开发和验证稳健的预后模型:这是一项回顾性多中心队列研究,调查肛门鳞状细胞癌初次化疗后的总生存率、局部控制率和无远处转移率。每个参与研究的放疗中心(n = 18)都将提取并整理患者数据。通过文献回顾和专家意见,确定候选预后因素。在建模之前,各中心将计算并交换汇总统计数据。主要分析将包括通过分布式学习,针对每种结果在各中心间建立并验证 Cox 比例危险模型。将报告特定时间点的相关结果和因素效应估计值,以便对未来患者的结果进行预测:atomCAT2 研究将对接受化疗放疗的肛门癌患者进行现有最大的跨机构队列分析。该分析旨在提供有关当前国际临床实践结果的信息,并通过更好地了解患者风险分层,帮助未来肛门癌临床试验的个性化设计。
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Development and validation of prognostic models for anal cancer outcomes using distributed learning: protocol for the international multi-centre atomCAT2 study.

Background: Anal cancer is a rare cancer with rising incidence. Despite the relatively good outcomes conferred by state-of-the-art chemoradiotherapy, further improving disease control and reducing toxicity has proven challenging. Developing and validating prognostic models using routinely collected data may provide new insights for treatment development and selection. However, due to the rarity of the cancer, it can be difficult to obtain sufficient data, especially from single centres, to develop and validate robust models. Moreover, multi-centre model development is hampered by ethical barriers and data protection regulations that often limit accessibility to patient data. Distributed (or federated) learning allows models to be developed using data from multiple centres without any individual-level patient data leaving the originating centre, therefore preserving patient data privacy. This work builds on the proof-of-concept three-centre atomCAT1 study and describes the protocol for the multi-centre atomCAT2 study, which aims to develop and validate robust prognostic models for three clinically important outcomes in anal cancer following chemoradiotherapy.

Methods: This is a retrospective multi-centre cohort study, investigating overall survival, locoregional control and freedom from distant metastasis after primary chemoradiotherapy for anal squamous cell carcinoma. Patient data will be extracted and organised at each participating radiotherapy centre (n = 18). Candidate prognostic factors have been identified through literature review and expert opinion. Summary statistics will be calculated and exchanged between centres prior to modelling. The primary analysis will involve developing and validating Cox proportional hazards models across centres for each outcome through distributed learning. Outcomes at specific timepoints of interest and factor effect estimates will be reported, allowing for outcome prediction for future patients.

Discussion: The atomCAT2 study will analyse one of the largest available cross-institutional cohorts of patients with anal cancer treated with chemoradiotherapy. The analysis aims to provide information on current international clinical practice outcomes and may aid the personalisation and design of future anal cancer clinical trials through contributing to a better understanding of patient risk stratification.

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