A conceptual framework for cautious escalation of anticancer treatment: How to optimize overall benefit and obviate the need for de-escalation trials

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL
I. Pourmir , H.K. Van Halteren , R. Elaidi , D. Trapani , F. Strasser , G. Vreugdenhil , M. Clarke
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引用次数: 0

Abstract

Background

The developmental workflow of the currently performed phase 1, 2 and 3 cancer trial stages lacks essential information required for the determination of the optimal efficacy threshold of new anticancer regimens. Due to this there is a serious risk of overdosing and/or treating for an unnecessary long time, leading to excess toxicity and a higher financial burden for society. But often post-approval de-escalation trials for dose-optimization and treatment de-intensification are not performed due to failing resources and time. Therefore, the developmental workflow needs to be restructured toward cautious systemic cancer treatment escalation, in order to guarantee optimal efficacy and sustainability.

Methods

In this manuscript we discuss opportunities to produce the information needed for cautious escalation, based on models of cancer growth and cancer kill kinetics as well as exploratory biomarkers, for the purpose of designing the optimal phase 3 superiority trial. Subsequently, we compare the sample size needed for a phase 3 superiority trial, followed by a necessary de-escalation trial with the sample size needed for a multi-arm phase 3 trial with intervention arms of differing intensity. All essential items are structured within a Framework for Cautious Escalation (FCE). The discussion uses illustrations from the breast cancer setting, but aims to be applicable for all cancers.

Results

The FCE is a promising model of clinical development in oncology to prevent overtreatment and associated issues, especially with regard to the number of repetitive treatment cycles. It will hopefully increase the relevance and success rate of clinical trials, to deliver improved patient-centric outcomes.

抗癌治疗谨慎升级的概念框架:如何优化总体疗效并避免降级试验的必要性
背景目前进行的 1、2 和 3 期癌症试验阶段的开发工作流程缺乏确定新抗癌疗法最佳疗效阈值所需的基本信息。因此,存在着用药过量和/或治疗时间过长的严重风险,从而导致毒性过大,加重社会的经济负担。但由于资源和时间的限制,往往无法进行批准后的剂量优化和治疗减量试验。因此,为了保证最佳疗效和可持续性,需要对开发工作流程进行重组,以实现谨慎的系统性癌症治疗升级。方法在本手稿中,我们讨论了根据癌症生长和癌症杀伤动力学模型以及探索性生物标志物来提供谨慎升级所需信息的机会,以便设计最佳的 3 期优势试验。随后,我们将 3 期优效试验(随后进行必要的降级试验)所需的样本量与具有不同强度干预臂的多臂 3 期试验所需的样本量进行了比较。所有基本项目都是在谨慎升级框架(FCE)内构建的。讨论以乳腺癌为例,但旨在适用于所有癌症。结果FCE是肿瘤学临床发展的一个很有前途的模式,可防止过度治疗及相关问题,尤其是重复治疗周期的数量。它有望提高临床试验的相关性和成功率,从而提供更好的以患者为中心的结果。
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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