Clinical Trials of Bispecific Antibody MDX-210 in Women with Advanced Breast or Ovarian Cancer that Overexpresses HER-2/neu
- 1 October 1995
- journal article
- clinical trial
- Published by Mary Ann Liebert Inc in Journal of Hematotherapy
- Vol. 4 (5) , 471-475
- https://doi.org/10.1089/scd.1.1995.4.471
Abstract
MDX-210 is a bispecific antibody (BsAb) that recognizes FcγR1 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 tumors 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.Keywords
This publication has 5 references indexed in Scilit:
- Involvement of the high-affinity receptor for IgG (Fc gamma RI; CD64) in enhanced tumor cell cytotoxicity of neutrophils during granulocyte colony-stimulating factor therapyBlood, 1993
- Enhanced antigen presentation using human Fc gamma receptor (monocyte/macrophage)-specific immunogens.The Journal of Immunology, 1992
- Identity of BCA200 and c-erbB-2 indicated by reactivity of monoclonal antibodies with recombinant c-erbB-2Molecular Immunology, 1991
- The determination of an immunologically active dose of interferon-gamma in patients with melanoma.Journal of Clinical Oncology, 1988
- Heteroantibody-mediated cytotoxicity: antibody to the high affinity Fc receptor for IgG mediates cytotoxicity by human monocytes that is enhanced by interferon-gamma and is not blocked by human IgG.The Journal of Immunology, 1986