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Envisioning the Future of Early Anticancer Drug Development

Overview
Journal Nat Rev Cancer
Specialty Oncology
Date 2010 Jun 11
PMID 20535131
Citations 98
Authors
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Abstract

The development of novel molecularly targeted cancer therapeutics remains slow and expensive with many late-stage failures. There is an urgent need to accelerate this process by improving early clinical anticancer drug evaluation through modern and rational trial designs that incorporate predictive, pharmacokinetic, pharmacodynamic, pharmacogenomic and intermediate end-point biomarkers. In this article, we discuss current approaches and propose strategies that will potentially maximize benefit to patients and expedite the regulatory approvals of new anticancer drugs.

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