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Ipilimumab and Cancer Immunotherapy: A New Hope for Advanced Stage Melanoma

Metastatic melanoma remains one of the most lethal and poorly treated forms of human cancer. Its incidence is on the rise, but no therapies offering improved survival rates have been developed over the last 40 years. This has changed with the recent Food and Drug Administration (FDA) approval of the...

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Autor principal: Mansh, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: YJBM 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238313/
https://www.ncbi.nlm.nih.gov/pubmed/22180676
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author Mansh, Matthew
author_facet Mansh, Matthew
author_sort Mansh, Matthew
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description Metastatic melanoma remains one of the most lethal and poorly treated forms of human cancer. Its incidence is on the rise, but no therapies offering improved survival rates have been developed over the last 40 years. This has changed with the recent Food and Drug Administration (FDA) approval of the CTLA-4 function blocking antibody Ipilimumab (Yervoy), proven to extend life in patients with previously treated or untreated metastatic melanoma [39,40]. CTLA-4 is a receptor that normally functions to inhibit inappropriate or prolonged activation of T-cells. This review presents the history of initial research into the function of the CTLA-4 receptor, the pre-clinical evidence for CTLA-4 blockade’s utility in cancer treatment, and the recent human clinical trials that have proven its efficacy in advanced stage melanoma. Ipilimumab represents one of a growing class of cancer immunotherapies currently under development and highlights both the promise and relative infancy of these agents in the clinical setting.
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spelling pubmed-32383132011-12-16 Ipilimumab and Cancer Immunotherapy: A New Hope for Advanced Stage Melanoma Mansh, Matthew Yale J Biol Med Focus: Immunology and Immunotherapeutics Metastatic melanoma remains one of the most lethal and poorly treated forms of human cancer. Its incidence is on the rise, but no therapies offering improved survival rates have been developed over the last 40 years. This has changed with the recent Food and Drug Administration (FDA) approval of the CTLA-4 function blocking antibody Ipilimumab (Yervoy), proven to extend life in patients with previously treated or untreated metastatic melanoma [39,40]. CTLA-4 is a receptor that normally functions to inhibit inappropriate or prolonged activation of T-cells. This review presents the history of initial research into the function of the CTLA-4 receptor, the pre-clinical evidence for CTLA-4 blockade’s utility in cancer treatment, and the recent human clinical trials that have proven its efficacy in advanced stage melanoma. Ipilimumab represents one of a growing class of cancer immunotherapies currently under development and highlights both the promise and relative infancy of these agents in the clinical setting. YJBM 2011-12 2011-12 /pmc/articles/PMC3238313/ /pubmed/22180676 Text en Copyright ©2011, Yale Journal of Biology and Medicine https://creativecommons.org/licenses/by-nc/3.0/This is an open access article distributed under the terms of the Creative Commons CC BY-NC license, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use the material for commercial purposes.
spellingShingle Focus: Immunology and Immunotherapeutics
Mansh, Matthew
Ipilimumab and Cancer Immunotherapy: A New Hope for Advanced Stage Melanoma
title Ipilimumab and Cancer Immunotherapy: A New Hope for Advanced Stage Melanoma
title_full Ipilimumab and Cancer Immunotherapy: A New Hope for Advanced Stage Melanoma
title_fullStr Ipilimumab and Cancer Immunotherapy: A New Hope for Advanced Stage Melanoma
title_full_unstemmed Ipilimumab and Cancer Immunotherapy: A New Hope for Advanced Stage Melanoma
title_short Ipilimumab and Cancer Immunotherapy: A New Hope for Advanced Stage Melanoma
title_sort ipilimumab and cancer immunotherapy: a new hope for advanced stage melanoma
topic Focus: Immunology and Immunotherapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238313/
https://www.ncbi.nlm.nih.gov/pubmed/22180676
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