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EpCAM an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges
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 erad...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360124/ https://www.ncbi.nlm.nih.gov/pubmed/17325709 http://dx.doi.org/10.1038/sj.bjc.6603505 |
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author | Chaudry, M A Sales, K Ruf, P Lindhofer, H Winslet, M C |
author_facet | Chaudry, M A Sales, K Ruf, P Lindhofer, H Winslet, M C |
author_sort | Chaudry, M A |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2360124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23601242009-09-10 EpCAM an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges Chaudry, M A Sales, K Ruf, P Lindhofer, H Winslet, M C Br J Cancer Minireview 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. Nature Publishing Group 2007-04-10 2007-02-27 /pmc/articles/PMC2360124/ /pubmed/17325709 http://dx.doi.org/10.1038/sj.bjc.6603505 Text en Copyright © 2007 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Minireview Chaudry, M A Sales, K Ruf, P Lindhofer, H Winslet, M C EpCAM an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges |
title | EpCAM an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges |
title_full | EpCAM an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges |
title_fullStr | EpCAM an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges |
title_full_unstemmed | EpCAM an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges |
title_short | EpCAM an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges |
title_sort | epcam an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges |
topic | Minireview |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360124/ https://www.ncbi.nlm.nih.gov/pubmed/17325709 http://dx.doi.org/10.1038/sj.bjc.6603505 |
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