Clinical trials of bispecific antibody MDX-210 in women with advanced breast or ovarian cancer that overexpresses HER-2/neu

J Hematother. 1995 Oct;4(5):471-5. doi: 10.1089/scd.1.1995.4.471.

Abstract

MDX-210 is a bispecific antibody (BsAb) that recognizes Fc gamma R1 on monocytes and macrophages and the cell surface product of the HER-2/neu oncogene, which is overexpressed on some breast and ovarian cancers. Clinical trials have demonstrated that treatment with MDX-210 is well tolerated and that MDX-210 is both immunologically and clinically active. Optimization of the dose and schedule of MDX-210 and development of combination treatments with cytokines that modulate immune effector cells will greatly enhance the efficacy of this novel BsAb construct for treatment of tumours that overexpress HER-2/neu. We envision that MDX-210 will be effective for treating patients with tumors that overexpress HER-2/neu, especially in the minimal disease setting.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase I
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antibodies, Anti-Idiotypic / biosynthesis
  • Antibodies, Bispecific / administration & dosage
  • Antibodies, Bispecific / adverse effects
  • Antibodies, Bispecific / immunology
  • Antibodies, Bispecific / therapeutic use*
  • Antibodies, Monoclonal / administration & dosage
  • Antibodies, Monoclonal / adverse effects
  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / therapeutic use*
  • Antibodies, Neoplasm / administration & dosage
  • Antibodies, Neoplasm / adverse effects
  • Antibodies, Neoplasm / immunology
  • Antibodies, Neoplasm / therapeutic use*
  • Antibody Specificity
  • Antibody-Dependent Cell Cytotoxicity
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / immunology
  • Breast Neoplasms / therapy*
  • Cohort Studies
  • Combined Modality Therapy
  • Cytokines / metabolism
  • Drug Administration Schedule
  • Female
  • Humans
  • Hypotension / chemically induced
  • Immunization, Passive
  • Neoplasm Proteins / immunology*
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / immunology
  • Ovarian Neoplasms / therapy*
  • Receptor, ErbB-2 / immunology*
  • Receptors, Fc / immunology
  • Receptors, IgG / immunology*

Substances

  • Antibodies, Anti-Idiotypic
  • Antibodies, Bispecific
  • Antibodies, Monoclonal
  • Antibodies, Neoplasm
  • Cytokines
  • Neoplasm Proteins
  • Receptors, Fc
  • Receptors, IgG
  • Receptor, ErbB-2