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The future of targeted kinase inhibitors in melanoma
Melanoma is a cancer of the pigment-producing cells of the body and its incidence is rising. Targeted inhibitors that act against kinases in the MAPK pathway are approved for BRAF-mutant metastatic cutaneous melanoma and increase patients’ survival. Response to these therapies is limited by drug res...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10187889/ https://www.ncbi.nlm.nih.gov/pubmed/35513054 http://dx.doi.org/10.1016/j.pharmthera.2022.108200 |
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author | Caksa, Signe Baqai, Usman Aplin, Andrew E. |
author_facet | Caksa, Signe Baqai, Usman Aplin, Andrew E. |
author_sort | Caksa, Signe |
collection | PubMed |
description | Melanoma is a cancer of the pigment-producing cells of the body and its incidence is rising. Targeted inhibitors that act against kinases in the MAPK pathway are approved for BRAF-mutant metastatic cutaneous melanoma and increase patients’ survival. Response to these therapies is limited by drug resistance and is less durable than with immune checkpoint inhibition. Conversely, rare melanoma subtypes have few therapeutic options for advanced disease and MAPK pathway targeting agents show minimal anti-tumor effects. Nevertheless, there is a future for targeted kinase inhibitors in melanoma: in new applications such as adjuvant or neoadjuvant therapy and in novel combinations with immunotherapies or other targeted therapies. Pre-clinical studies continue to identify tumor dependencies and their corresponding actionable drug targets, paving the way for rational targeted kinase inhibitor combinations as a personalized medicine approach for melanoma. |
format | Online Article Text |
id | pubmed-10187889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-101878892023-05-16 The future of targeted kinase inhibitors in melanoma Caksa, Signe Baqai, Usman Aplin, Andrew E. Pharmacol Ther Article Melanoma is a cancer of the pigment-producing cells of the body and its incidence is rising. Targeted inhibitors that act against kinases in the MAPK pathway are approved for BRAF-mutant metastatic cutaneous melanoma and increase patients’ survival. Response to these therapies is limited by drug resistance and is less durable than with immune checkpoint inhibition. Conversely, rare melanoma subtypes have few therapeutic options for advanced disease and MAPK pathway targeting agents show minimal anti-tumor effects. Nevertheless, there is a future for targeted kinase inhibitors in melanoma: in new applications such as adjuvant or neoadjuvant therapy and in novel combinations with immunotherapies or other targeted therapies. Pre-clinical studies continue to identify tumor dependencies and their corresponding actionable drug targets, paving the way for rational targeted kinase inhibitor combinations as a personalized medicine approach for melanoma. 2022-11 2022-05-02 /pmc/articles/PMC10187889/ /pubmed/35513054 http://dx.doi.org/10.1016/j.pharmthera.2022.108200 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Caksa, Signe Baqai, Usman Aplin, Andrew E. The future of targeted kinase inhibitors in melanoma |
title | The future of targeted kinase inhibitors in melanoma |
title_full | The future of targeted kinase inhibitors in melanoma |
title_fullStr | The future of targeted kinase inhibitors in melanoma |
title_full_unstemmed | The future of targeted kinase inhibitors in melanoma |
title_short | The future of targeted kinase inhibitors in melanoma |
title_sort | future of targeted kinase inhibitors in melanoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10187889/ https://www.ncbi.nlm.nih.gov/pubmed/35513054 http://dx.doi.org/10.1016/j.pharmthera.2022.108200 |
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