EpCAM an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges

Br J Cancer. 2007 Apr 10;96(7):1013-9. doi: 10.1038/sj.bjc.6603505. Epub 2007 Feb 27.


Despite advances in surgery and adjuvant regimes, gastrointestinal malignancy remains a major cause of neoplastic mortality. Immunotherapy is an emerging and now successful treatment modality for numerous cancers that relies on the manipulation of the immune system and its effector functions to eradicate tumour cells. The discovery that the pan-epithelial homotypic cell adhesion molecule EpCAM is differentially expressed on gastrointestinal tumours has made this a viable target for immunotherapy. Clinical trials using naked anti EpCAM antibody, immunoconjugates, anti-idiotypic and dendritic cell vaccines have met variable success. The murine IgG2a Edrecolomab was shown to reduce mortality and morbidity at a level slightly lower than treatment with 5FU and Levamisole when administered to patients with advanced colorectal carcinoma in a large randomised controlled trial. Fully human and trifunctional antibodies that specifically recruit CD3-positive lymphocytes are now being tested clinically in the treatment of minimal residual disease and ascites. Although clinical trials are in their infancy, the future may bring forth an EpCAM mediated approach for the effective activation and harnessing of the immune system to destroy a pathological aberrance that has otherwise largely escaped its attention.

Publication types

  • Review

MeSH terms

  • Antigens, Neoplasm / metabolism
  • CD3 Complex
  • Cell Adhesion Molecules / antagonists & inhibitors*
  • Cell Adhesion Molecules / metabolism
  • Epithelial Cell Adhesion Molecule
  • Gastrointestinal Neoplasms / metabolism
  • Gastrointestinal Neoplasms / therapy*
  • Humans
  • Immunotherapy*


  • Antigens, Neoplasm
  • CD3 Complex
  • Cell Adhesion Molecules
  • Epithelial Cell Adhesion Molecule