Seminars in Oncology
Volume 33, Supplement 11 , Pages 24-27, December 2006

Successful Gastrointestinal Cancer Drug Development

  • J. Randolph Hecht

      Affiliations

    • Corresponding Author InformationAddress reprint requests to J. Randolph Hecht, MD, UCLA GI Oncology Program, UCLA School of Medicine, 2338G PVUB, 10945 Le Conte Ave, Los Angeles, CA 90095, USA

University of California–Los Angeles GI Oncology Program, UCLA School of Medicine, Los Angeles, CA

A large number of new drugs have been approved over the past 10 years for the treatment of both common and rare gastrointestinal malignancies. Many other agents, however, have failed at a great cost of financial and patient resources. Drug development must identify potentially active compounds and reveal the most effective and least toxic manner and population in which to administer compounds. Pharmaceutical companies must show therapeutic efficacy and achieve regulatory approval as well as success in the marketplace to recoup their investment. It is worth examining successful examples of drug development such as imatinib, delayed but eventually successful agents such as oxaliplatin, as well as failures such as SU-5416, and applying those lessons to current and future drug development.

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 Dr Hecht has received research grant support from Amgen, Novartis, Roche, and Genvec, and has served as a consultant to Genentech.

PII: S0093-7754(06)00378-2

doi:10.1053/j.seminoncol.2006.10.001

Seminars in Oncology
Volume 33, Supplement 11 , Pages 24-27, December 2006