Hisato Kawakami, Kimio Yonesaka1. 1. Department of Medical Oncology, Kinki University Faculty of Medicine, 377-2 Ohno-higashi, Osaka- Sayama, Osaka 589-8511, Japan. yonesaka2002@yahoo.co.jp.
Abstract
UNLABELLED: Emerging evidence suggests that human epidermal growth factor receptor 3 plays a critical role in cell-survival and drug-resistance in cancer cells. Several kinds of agents targeting this receptor are currently progressing through preclinical or clinical investigations. These agents are usually monoclonal antibodies with unique characteristics, and some have shown efficacy and been welltolerated in clinical trials. For example, patritumab and seribantumab are thought to compete with ligand binding and have proven efficacy for some malignancies in Phase II clinical trials. LJM716 locks the human epidermal growth factor receptor 3 in the inactive conformation in both ligand-dependent and - independent cancers. Lumretuzumab is a glycoengineered antibody, which enhances antibody-dependent cell-mediated cytotoxicity. Duligotumab is an antibody that targets both the human epidermal growth factor receptors 1 and 3. Heregulin is a human epidermal growth factor receptor 3 ligand that represents an encouraging candidate biomarker for the prediction of the efficacy of agents targeting this receptor. CONCLUSION: A number of antibodies that interact with human epidermal growth factor receptors have been evaluated for clinical use. Ongoing clinical trials will address the remaining issues related to optimization of drug combination therapy and improving the targeting of each agent to the most appropriate individuals.
UNLABELLED: Emerging evidence suggests that humanepidermal growth factor receptor 3 plays a critical role in cell-survival and drug-resistance in cancer cells. Several kinds of agents targeting this receptor are currently progressing through preclinical or clinical investigations. These agents are usually monoclonal antibodies with unique characteristics, and some have shown efficacy and been welltolerated in clinical trials. For example, patritumab and seribantumab are thought to compete with ligand binding and have proven efficacy for some malignancies in Phase II clinical trials. LJM716 locks the humanepidermal growth factor receptor 3 in the inactive conformation in both ligand-dependent and - independent cancers. Lumretuzumab is a glycoengineered antibody, which enhances antibody-dependent cell-mediated cytotoxicity. Duligotumab is an antibody that targets both the humanepidermal growth factor receptors 1 and 3. Heregulin is a humanepidermal growth factor receptor 3 ligand that represents an encouraging candidate biomarker for the prediction of the efficacy of agents targeting this receptor. CONCLUSION: A number of antibodies that interact with human epidermal growth factor receptors have been evaluated for clinical use. Ongoing clinical trials will address the remaining issues related to optimization of drug combination therapy and improving the targeting of each agent to the most appropriate individuals.
Authors: Emily Capone; Francesco Giansanti; Sara Ponziani; Alessia Lamolinara; Manuela Iezzi; Annamaria Cimini; Francesco Angelucci; Rossana La Sorda; Vincenzo De Laurenzi; Pier Giorgio Natali; Rodolfo Ippoliti; Stefano Iacobelli; Gianluca Sala Journal: Oncotarget Date: 2017-09-08
Authors: Maria Rosestedt; Ken G Andersson; Sara S Rinne; Charles Dahlsson Leitao; Bogdan Mitran; Anzhelika Vorobyeva; Stefan Ståhl; John Löfblom; Vladimir Tolmachev; Anna Orlova Journal: Sci Rep Date: 2019-05-01 Impact factor: 4.379