EgF Receptor Mabs and Chemotherapy/Characterization of Synergistic Interactions Between Cytotoxic Agents and Inhibitors of the Tyrosine Kinase Growth Factor Receptor Signalling Cascade

Abstract

Human epidermal growth factor receptor (EGFR, HER1) and HER2 are transmembrane receptors possessing intrinsic tyrosine kinase activity. Preclinical and more recently, clinical demonstration of synergism between antibodies directed at these receptors and chemotherapeutic agents has focused our present efforts on the characterization of synergistic interactions between cytotoxic drugs and inhibitors of the tyrosine kinase growth factor signalling cascade. While we have encountered obstacles, both clinical toxicity as well as operational difficulties, in the investigation of the chimeric monoclonal antibody C225 (directed at EGFR) + paclitaxel, as summarized within this report, we have subsequently proceeded rapidly and successfully with clinical evaluation of weekly trastuzumab (HER2-directed) + weekly paclitaxel. The present report describes our most recent efforts to molecularly characterize this synergy, to perform preclinical evaluation of antitubulin agents (taxanes, vincas, and epothilones) alone and in combination with famesyl protein transferase inhibitors in mammary carcinoma cells, and to better define molecular predictors of response to inhibitors of mitogenic signal transduction, taxanes, and combinations of these agents.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1998
Accession Number
ADA378229

Entities

People

  • Andrew D. Seidman

Organizations

  • Memorial Sloan Kettering Cancer Center

Tags

DTIC Thesaurus Topics

  • Antibodies
  • Breast Cancer
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Chemotherapeutic Agents
  • Chemotherapy
  • Clinical Trials
  • Cytotoxins
  • Databases
  • Growth Factors
  • Hematologic Diseases
  • Inhibitors
  • Neoplasms
  • New York
  • Proteins
  • Toxicity

Fields of Study

  • Biology

Readers

  • Cellular and Molecular Pathways of Apoptosis.
  • Oncology (Cancer Research).