Critical parameters in targeted drug development: the pharmacological audit trail

被引:55
作者
Banerji, Udai [1 ,2 ]
Workman, Paul [1 ]
机构
[1] Inst Canc Res, Canc Res UK Canc Therapeut Unit, 15 Cotswold Rd, London SM2 5NG, England
[2] Royal Marsden NHS Fdn Trust, London, England
关键词
Pharmacological audit trail; Biomarkers; Pharmacodynamics; Pharmacokinetics; HISTONE DEACETYLASE INHIBITOR; PHARMACODYNAMIC END-POINTS; RESISTANT PROSTATE-CANCER; CHRONIC MYELOID-LEUKEMIA; CIRCULATING TUMOR-CELLS; EARLY CLINICAL-TRIALS; 1ST-IN-HUMAN PHASE-I; DOSE-ESCALATION; BREAST-CANCER; LUNG-CANCER;
D O I
10.1053/j.seminoncol.2016.06.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Pharmacological Audit Trail (PhAT) comprises a set of critical questions that need to be asked during discovery and development of an anticancer drug. Key aspects include: (1) defining a patient population; (2) establishing pharmacokinetic characteristics; (3) providing evidence of target engagement, pathway modulation, and biological effect with proof of concept pharmacodynamic biomarkers; (4) determining intermediate biomarkers of response; (5) assessing tumor response; and (6) determining how to overcome resistance by combination or sequential therapy and new target/drug discovery. The questions asked in the PhAT should be viewed as a continuum and not used in isolation. Different drug development programmes derive different types of benefit from these questions. The PhAT is critical in making go-no-go decisions in the development of currently studied drugs and will continue to be relevant to discovery and development of future generations of anticancer agents. (C) 2016 The Authors. Published by Elsevier Inc.
引用
收藏
页码:436 / 445
页数:10
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