New Antibody Conjugates in Cancer Therapy

Targeting of radiation, drugs, and protein toxins to cancers selectively with monoclonal antibodies (MAbs) has been a topic of considerable interest and an area of continued development. Radioimmunotherapy (RAIT) of lymphoma using directly labeled MAbs is of current interest after approval of two ra...

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Main Authors: Serengulam V. Govindan, David M. Goldenberg
Format: Article
Language:English
Published: Hindawi Limited 2010-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1100/tsw.2010.191
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spelling doaj-e5cf60bf37d14fdd987f2caff642afe22020-11-24T21:26:25ZengHindawi LimitedThe Scientific World Journal1537-744X2010-01-01102070208910.1100/tsw.2010.191New Antibody Conjugates in Cancer TherapySerengulam V. Govindan0David M. Goldenberg1Immunomedics, Inc., Morris Plains, NJ, USAGarden State Cancer Center at the Center for Molecular Medicine and Immunology, Belleville, NJ, USATargeting of radiation, drugs, and protein toxins to cancers selectively with monoclonal antibodies (MAbs) has been a topic of considerable interest and an area of continued development. Radioimmunotherapy (RAIT) of lymphoma using directly labeled MAbs is of current interest after approval of two radiolabeled anti-CD20 MAbs, as illustrated with the near 100% overall response rate obtained in a recent clinical trial using an investigational radiolabeled anti-CD22 MAb, 90Y-epratuzumab. The advantage of pretargeted RAIT over directly labeled MAbs is continuing to be validated in preclinical models of lymphoma and solid tumors. Importantly, the advantages of combining RAIT with radiation sensitizers, with immunotherapy, or a drug conjugate targeting a different antigen are being studied clinically and preclinically. The area of drug-conjugated antibodies is progressing with encouraging data published for the trastuzumab-DM1 conjugate in a phase I clinical trial in HER2-positive breast cancer. The Dock-and-Lock platform technology has contributed to the design and the evaluation of complex antibody-cytokine and antibody-toxin conjugates. This review describes the advances made in these areas, with illustrations taken from advances made in the authors' institutions.http://dx.doi.org/10.1100/tsw.2010.191
collection DOAJ
language English
format Article
sources DOAJ
author Serengulam V. Govindan
David M. Goldenberg
spellingShingle Serengulam V. Govindan
David M. Goldenberg
New Antibody Conjugates in Cancer Therapy
The Scientific World Journal
author_facet Serengulam V. Govindan
David M. Goldenberg
author_sort Serengulam V. Govindan
title New Antibody Conjugates in Cancer Therapy
title_short New Antibody Conjugates in Cancer Therapy
title_full New Antibody Conjugates in Cancer Therapy
title_fullStr New Antibody Conjugates in Cancer Therapy
title_full_unstemmed New Antibody Conjugates in Cancer Therapy
title_sort new antibody conjugates in cancer therapy
publisher Hindawi Limited
series The Scientific World Journal
issn 1537-744X
publishDate 2010-01-01
description Targeting of radiation, drugs, and protein toxins to cancers selectively with monoclonal antibodies (MAbs) has been a topic of considerable interest and an area of continued development. Radioimmunotherapy (RAIT) of lymphoma using directly labeled MAbs is of current interest after approval of two radiolabeled anti-CD20 MAbs, as illustrated with the near 100% overall response rate obtained in a recent clinical trial using an investigational radiolabeled anti-CD22 MAb, 90Y-epratuzumab. The advantage of pretargeted RAIT over directly labeled MAbs is continuing to be validated in preclinical models of lymphoma and solid tumors. Importantly, the advantages of combining RAIT with radiation sensitizers, with immunotherapy, or a drug conjugate targeting a different antigen are being studied clinically and preclinically. The area of drug-conjugated antibodies is progressing with encouraging data published for the trastuzumab-DM1 conjugate in a phase I clinical trial in HER2-positive breast cancer. The Dock-and-Lock platform technology has contributed to the design and the evaluation of complex antibody-cytokine and antibody-toxin conjugates. This review describes the advances made in these areas, with illustrations taken from advances made in the authors' institutions.
url http://dx.doi.org/10.1100/tsw.2010.191
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