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Update on use of aldesleukin for treatment of high-risk metastatic melanoma

High-dose interleukin-2 has been used for the treatment of metastatic melanoma since 1998 based on data proving durable complete responses in up to 10% of treated patients. The immunomodulatory effects of this critical cytokine have been instrumental in the development of immunotherapy for melanoma...

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Autores principales: Amaria, Rodabe N, Reuben, Alexandre, Cooper, Zachary A, Wargo, Jennifer A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918260/
https://www.ncbi.nlm.nih.gov/pubmed/27471714
http://dx.doi.org/10.2147/ITT.S61590
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author Amaria, Rodabe N
Reuben, Alexandre
Cooper, Zachary A
Wargo, Jennifer A
author_facet Amaria, Rodabe N
Reuben, Alexandre
Cooper, Zachary A
Wargo, Jennifer A
author_sort Amaria, Rodabe N
collection PubMed
description High-dose interleukin-2 has been used for the treatment of metastatic melanoma since 1998 based on data proving durable complete responses in up to 10% of treated patients. The immunomodulatory effects of this critical cytokine have been instrumental in the development of immunotherapy for melanoma and other cancers. However, with the advent of new therapies, its use as a front-line agent has come into question. Nonetheless, there is still a role for interleukin-2 as monotherapy, as well as in combination with other agents and in clinical trials. In this article, we review preclinical and clinical data regarding interleukin-2, its pharmacology and mechanism of action, its toxicity profile, and its use in ongoing and planned clinical trials. We also explore the future of this agent within the treatment landscape for melanoma.
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spelling pubmed-49182602016-07-28 Update on use of aldesleukin for treatment of high-risk metastatic melanoma Amaria, Rodabe N Reuben, Alexandre Cooper, Zachary A Wargo, Jennifer A Immunotargets Ther Review High-dose interleukin-2 has been used for the treatment of metastatic melanoma since 1998 based on data proving durable complete responses in up to 10% of treated patients. The immunomodulatory effects of this critical cytokine have been instrumental in the development of immunotherapy for melanoma and other cancers. However, with the advent of new therapies, its use as a front-line agent has come into question. Nonetheless, there is still a role for interleukin-2 as monotherapy, as well as in combination with other agents and in clinical trials. In this article, we review preclinical and clinical data regarding interleukin-2, its pharmacology and mechanism of action, its toxicity profile, and its use in ongoing and planned clinical trials. We also explore the future of this agent within the treatment landscape for melanoma. Dove Medical Press 2015-04-07 /pmc/articles/PMC4918260/ /pubmed/27471714 http://dx.doi.org/10.2147/ITT.S61590 Text en © 2015 Amaria et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Amaria, Rodabe N
Reuben, Alexandre
Cooper, Zachary A
Wargo, Jennifer A
Update on use of aldesleukin for treatment of high-risk metastatic melanoma
title Update on use of aldesleukin for treatment of high-risk metastatic melanoma
title_full Update on use of aldesleukin for treatment of high-risk metastatic melanoma
title_fullStr Update on use of aldesleukin for treatment of high-risk metastatic melanoma
title_full_unstemmed Update on use of aldesleukin for treatment of high-risk metastatic melanoma
title_short Update on use of aldesleukin for treatment of high-risk metastatic melanoma
title_sort update on use of aldesleukin for treatment of high-risk metastatic melanoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918260/
https://www.ncbi.nlm.nih.gov/pubmed/27471714
http://dx.doi.org/10.2147/ITT.S61590
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