From bench to bedside: lessons learned in translating preclinical studies in cancer drug development

J Natl Cancer Inst. 2013 Oct 2;105(19):1441-56. doi: 10.1093/jnci/djt209. Epub 2013 Sep 19.

Abstract

The development of targeted agents in oncology has rapidly expanded over the past 2 decades and has led to clinically significant improvements in the treatment of numerous cancers. Unfortunately, not all success at the bench in preclinical experiments has translated to success at the bedside. As preclinical studies shift toward defining proof of mechanism, patient selection, and rational drug combinations, it is critical to understand the lessons learned from prior translational studies to gain an understanding of prior drug development successes and failures. By learning from prior drug development, future translational studies will provide more clinically relevant data, and the underlying hope is that the clinical success rate will improve and the treatment of patients with ineffective targeted therapy will be limited.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Angiogenesis Inhibitors / pharmacology
  • Animals
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / toxicity
  • Cell Transformation, Neoplastic / drug effects*
  • Clinical Trials as Topic
  • Drug Combinations
  • Drug Design*
  • Drug Evaluation, Preclinical*
  • ErbB Receptors / antagonists & inhibitors
  • Humans
  • Molecular Targeted Therapy*
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism
  • Neovascularization, Pathologic / drug therapy*
  • Neovascularization, Pathologic / prevention & control
  • Patient Satisfaction
  • Patient Selection
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Translational Research, Biomedical*
  • Vascular Endothelial Growth Factor A / antagonists & inhibitors
  • Xenograft Model Antitumor Assays

Substances

  • Angiogenesis Inhibitors
  • Antineoplastic Agents
  • Drug Combinations
  • Vascular Endothelial Growth Factor A
  • ErbB Receptors
  • Protein-Tyrosine Kinases