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Review of catumaxomab in the treatment of malignant ascites

Malignant ascites is frequently found with various solid tumors, and no established treatment options exist, apart from symptomatic paracentesis. Catumaxomab, a trifunctional bispecific monoclonal antibody, has two binding specificities directed to epithelial cell adhesion molecule (EpCAM) and the T...

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Detalles Bibliográficos
Autor principal: Sebastian, Martin
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004584/
https://www.ncbi.nlm.nih.gov/pubmed/21188120
http://dx.doi.org/10.2147/CMR.S14115
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author Sebastian, Martin
author_facet Sebastian, Martin
author_sort Sebastian, Martin
collection PubMed
description Malignant ascites is frequently found with various solid tumors, and no established treatment options exist, apart from symptomatic paracentesis. Catumaxomab, a trifunctional bispecific monoclonal antibody, has two binding specificities directed to epithelial cell adhesion molecule (EpCAM) and the T cell antigen CD3. With its Fc-fragment, catumaxomab additionally binds accessory cells, including dendritic cells, macrophages, and natural killer cells. The trifunctional approach thus leads to a major histocompatibility complex-unrestricted but specific killing of epithelial tumor cells without need for preactivation or external costimulation. Because EpCAM is expressed in most solid tumors, but not in tissue of mesothelial origin, intraperitoneal treatment with catumaxomab is tumor-specific. Intraperitoneal treatment with catumaxomab resulted in a significant prolongation of puncture-free survival in patients with malignant ascites due to epithelial cancer. Catumaxomab has been approved in Europe for the intraperitoneal treatment of malignant ascites in patients with EpCAM-positive epithelial tumors where standard therapy is not available or no longer feasible.
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spelling pubmed-30045842010-12-23 Review of catumaxomab in the treatment of malignant ascites Sebastian, Martin Cancer Manag Res Review Malignant ascites is frequently found with various solid tumors, and no established treatment options exist, apart from symptomatic paracentesis. Catumaxomab, a trifunctional bispecific monoclonal antibody, has two binding specificities directed to epithelial cell adhesion molecule (EpCAM) and the T cell antigen CD3. With its Fc-fragment, catumaxomab additionally binds accessory cells, including dendritic cells, macrophages, and natural killer cells. The trifunctional approach thus leads to a major histocompatibility complex-unrestricted but specific killing of epithelial tumor cells without need for preactivation or external costimulation. Because EpCAM is expressed in most solid tumors, but not in tissue of mesothelial origin, intraperitoneal treatment with catumaxomab is tumor-specific. Intraperitoneal treatment with catumaxomab resulted in a significant prolongation of puncture-free survival in patients with malignant ascites due to epithelial cancer. Catumaxomab has been approved in Europe for the intraperitoneal treatment of malignant ascites in patients with EpCAM-positive epithelial tumors where standard therapy is not available or no longer feasible. Dove Medical Press 2010-11-08 /pmc/articles/PMC3004584/ /pubmed/21188120 http://dx.doi.org/10.2147/CMR.S14115 Text en © 2010 Sebastian, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Sebastian, Martin
Review of catumaxomab in the treatment of malignant ascites
title Review of catumaxomab in the treatment of malignant ascites
title_full Review of catumaxomab in the treatment of malignant ascites
title_fullStr Review of catumaxomab in the treatment of malignant ascites
title_full_unstemmed Review of catumaxomab in the treatment of malignant ascites
title_short Review of catumaxomab in the treatment of malignant ascites
title_sort review of catumaxomab in the treatment of malignant ascites
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004584/
https://www.ncbi.nlm.nih.gov/pubmed/21188120
http://dx.doi.org/10.2147/CMR.S14115
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