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Herceptin.

H M Shepard1, P Jin, D J Slamon

  • 1Receptor BioLogix Inc., 3350 W. Bayshore Road. Palo Alto, CA 94303, USA. hms@rblx.com

Handbook of Experimental Pharmacology
|December 12, 2007
PubMed
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This review details the development of Herceptin, a targeted therapy for HER2-positive breast cancer. It highlights key decisions in creating the first successful tyrosine kinase inhibitor for cancer treatment.

Area of Science:

  • Oncology
  • Pharmacology
  • Molecular Biology

Background:

  • The human epidermal growth factor receptor-2 (HER2) is a validated target for cancer therapy.
  • Herceptin is a monoclonal antibody approved for HER2-positive breast cancer treatment, used in over 150,000 women.
  • Understanding the developmental history of Herceptin offers insights into targeted drug discovery.

Observation:

  • The specific developmental history, critical decision points, and rationale for pursuing a monoclonal antibody approach for HER2 have not been fully documented.
  • This review aims to elucidate these pivotal events and decisions.
  • The development of Herceptin represents a significant milestone in targeted cancer therapeutics.

Findings:

  • The review details the critical events and decision-making processes that led to the development of Herceptin.

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  • It explains the strategic choices made during the drug discovery and development program.
  • Herceptin emerged as the first therapeutic agent successfully targeting tyrosine kinases in cancer.
  • Implications:

    • Sharing the Herceptin development experience can inform future drug discovery and development processes.
    • The success of Herceptin provides a model for developing targeted therapies against other HER family members.
    • New therapeutic strategies and future directions for targeting the HER family are discussed.