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药物与诊断联合开发:挑战与问题

Drug-diagnostic co-development: challenges and issues.

作者信息

Shimazawa Rumiko, Ikeda Masayuki

机构信息

a Graduate School of Medicine , Osaka University , Osaka , Japan.

b Department of Medical Informatics , Kagawa University Hospital , Kagawa , Japan.

出版信息

Expert Rev Mol Diagn. 2016;16(2):187-204. doi: 10.1586/14737159.2016.1132163. Epub 2016 Jan 13.

Abstract

Diagnostic tests have become increasingly important for optimizing drug use. Ideally, a companion diagnostic test is developed concurrently with a corresponding therapeutic product (co-development). However, the diagnostic test may also be developed to optimize treatment with previously approved therapeutic agents (follow-up-development). In co-development, the effectiveness of an agent in marker-defined patients is confirmed by an enrichment trial design. In follow-up-development, a biomarker is validated by prospective and/or retrospective analyses of unselected design trials. A prospectively designed trial is the gold-standard approach to biomarker validation, but retrospective validation can be used to efficiently determine effective treatments for marker-defined patients. Accumulation and systematization of examples of drug-diagnostic development will aid in the effective development of companion diagnostics.

摘要

诊断测试对于优化药物使用变得越来越重要。理想情况下,伴随诊断测试与相应的治疗产品同时开发(共同开发)。然而,诊断测试也可以开发用于优化使用先前批准的治疗药物的治疗(后续开发)。在共同开发中,通过富集试验设计确认药物在标志物定义的患者中的有效性。在后续开发中,通过对未选择设计试验的前瞻性和/或回顾性分析来验证生物标志物。前瞻性设计试验是生物标志物验证的金标准方法,但回顾性验证可用于有效确定标志物定义患者的有效治疗方法。药物 - 诊断开发实例的积累和系统化将有助于伴随诊断的有效开发。

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