Therapeutic Monoclonal Antibodies in Clinical Practice against Cancer | Bentham Science
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Anti-Cancer Agents in Medicinal Chemistry

Editor-in-Chief

ISSN (Print): 1871-5206
ISSN (Online): 1875-5992

Review Article

Therapeutic Monoclonal Antibodies in Clinical Practice against Cancer

Author(s): Navgeet Kaur*, Anju Goyal and Rakesh K. Sindhu

Volume 20, Issue 16, 2020

Page: [1895 - 1907] Pages: 13

DOI: 10.2174/1871520620666200703191653

Price: $65

Open Access Journals Promotions 2
Abstract

The importance of monoclonal antibodies in oncology has increased drastically following the discovery of Milstein and Kohler. Since the first approval of the monoclonal antibody, i.e. Rituximab in 1997 by the FDA, there was a decline in further applications but this number has significantly increased over the last three decades for various therapeutic applications due to the lesser side effects in comparison to the traditional chemotherapy methods. Presently, numerous monoclonal antibodies have been approved and many are in queue for approval as a strong therapeutic agent for treating hematologic malignancies and solid tumors. The main target checkpoints for the monoclonal antibodies against cancer cells include EGFR, VEGF, CD and tyrosine kinase which are overexpressed in malignant cells. Other immune checkpoints like CTLA-4, PD-1 and PD-1 receptors targeted by the recently developed antibodies increase the capability of the immune system in destroying the cancerous cells. Here, in this review, the mechanism of action, uses and target points of the approved mAbs against cancer have been summarized.

Keywords: Monoclonal antibodies (mAbs), therapeutic application, FDA approvals, EGFR, VEGF, CD, CTLA-4, PD-1, cancer.

Graphical Abstract
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