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CDK4/6 Inhibitors in Melanoma: A Comprehensive Review

Historically, metastatic melanoma was considered a highly lethal disease. However, recent advances in drug development have allowed a significative improvement in prognosis. In particular, BRAF/MEK inhibitors and anti-PD1 antibodies have completely revolutionized the management of this disease. None...

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Autores principales: Garutti, Mattia, Targato, Giada, Buriolla, Silvia, Palmero, Lorenza, Minisini, Alessandro Marco, Puglisi, Fabio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227121/
https://www.ncbi.nlm.nih.gov/pubmed/34071228
http://dx.doi.org/10.3390/cells10061334
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author Garutti, Mattia
Targato, Giada
Buriolla, Silvia
Palmero, Lorenza
Minisini, Alessandro Marco
Puglisi, Fabio
author_facet Garutti, Mattia
Targato, Giada
Buriolla, Silvia
Palmero, Lorenza
Minisini, Alessandro Marco
Puglisi, Fabio
author_sort Garutti, Mattia
collection PubMed
description Historically, metastatic melanoma was considered a highly lethal disease. However, recent advances in drug development have allowed a significative improvement in prognosis. In particular, BRAF/MEK inhibitors and anti-PD1 antibodies have completely revolutionized the management of this disease. Nonetheless, not all patients derive a benefit or a durable benefit from these therapies. To overtake this challenges, new clinically active compounds are being tested in the context of clinical trials. CDK4/6 inhibitors are drugs already available in clinical practice and preliminary evidence showed a promising activity also in melanoma. Herein we review the available literature to depict a comprehensive landscape about CDK4/6 inhibitors in melanoma. We present the molecular and genetic background that might justify the usage of these drugs, the preclinical evidence, the clinical available data, and the most promising ongoing clinical trials.
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spelling pubmed-82271212021-06-26 CDK4/6 Inhibitors in Melanoma: A Comprehensive Review Garutti, Mattia Targato, Giada Buriolla, Silvia Palmero, Lorenza Minisini, Alessandro Marco Puglisi, Fabio Cells Review Historically, metastatic melanoma was considered a highly lethal disease. However, recent advances in drug development have allowed a significative improvement in prognosis. In particular, BRAF/MEK inhibitors and anti-PD1 antibodies have completely revolutionized the management of this disease. Nonetheless, not all patients derive a benefit or a durable benefit from these therapies. To overtake this challenges, new clinically active compounds are being tested in the context of clinical trials. CDK4/6 inhibitors are drugs already available in clinical practice and preliminary evidence showed a promising activity also in melanoma. Herein we review the available literature to depict a comprehensive landscape about CDK4/6 inhibitors in melanoma. We present the molecular and genetic background that might justify the usage of these drugs, the preclinical evidence, the clinical available data, and the most promising ongoing clinical trials. MDPI 2021-05-28 /pmc/articles/PMC8227121/ /pubmed/34071228 http://dx.doi.org/10.3390/cells10061334 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Garutti, Mattia
Targato, Giada
Buriolla, Silvia
Palmero, Lorenza
Minisini, Alessandro Marco
Puglisi, Fabio
CDK4/6 Inhibitors in Melanoma: A Comprehensive Review
title CDK4/6 Inhibitors in Melanoma: A Comprehensive Review
title_full CDK4/6 Inhibitors in Melanoma: A Comprehensive Review
title_fullStr CDK4/6 Inhibitors in Melanoma: A Comprehensive Review
title_full_unstemmed CDK4/6 Inhibitors in Melanoma: A Comprehensive Review
title_short CDK4/6 Inhibitors in Melanoma: A Comprehensive Review
title_sort cdk4/6 inhibitors in melanoma: a comprehensive review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227121/
https://www.ncbi.nlm.nih.gov/pubmed/34071228
http://dx.doi.org/10.3390/cells10061334
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