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Advanced Acral Melanoma Therapies: Current Status and Future Directions
Melanoma is one of the deadliest malignancies. Its incidence has been significantly increasing in most countries in recent decades. Acral melanoma (AM), a peculiar subgroup of melanoma occurring on the palms, soles, and nails, is the main subtype of melanoma in people of color and is extremely rare...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526689/ https://www.ncbi.nlm.nih.gov/pubmed/36125617 http://dx.doi.org/10.1007/s11864-022-01007-6 |
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author | Zhang, Yiqun Lan, Shijie Wu, Di |
author_facet | Zhang, Yiqun Lan, Shijie Wu, Di |
author_sort | Zhang, Yiqun |
collection | PubMed |
description | Melanoma is one of the deadliest malignancies. Its incidence has been significantly increasing in most countries in recent decades. Acral melanoma (AM), a peculiar subgroup of melanoma occurring on the palms, soles, and nails, is the main subtype of melanoma in people of color and is extremely rare in Caucasians. Although great progress has been made in melanoma treatment in recent years, patients with AM have shown limited benefit from current therapies and thus consequently have worse overall survival rates. Achieving durable therapeutic responses in this high-risk melanoma subtype represents one of the greatest challenges in the field. The frequency of BRAF mutations in AM is much lower than that in cutaneous melanoma, which prevents most AM patients from receiving treatment with BRAF inhibitors. However, AM has more frequent mutations such as KIT and CDK4/6, so targeted therapy may still improve the survival of some AM patients in the future. AM may be less susceptible to immune checkpoint inhibitors because of the poor immunogenicity. Therefore, how to enhance the immune response to the tumor cells may be the key to the application of immune checkpoint inhibitors in advanced AM. Anti-angiogenic drugs, albumin paclitaxel, or interferons are thought to enhance the effectiveness of immune checkpoint inhibitors. Combination therapies based on the backbone of PD-1 are more likely to provide greater clinical benefits. Understanding the molecular landscapes and immune microenvironment of AM will help optimize our combinatory strategies. |
format | Online Article Text |
id | pubmed-9526689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-95266892022-10-03 Advanced Acral Melanoma Therapies: Current Status and Future Directions Zhang, Yiqun Lan, Shijie Wu, Di Curr Treat Options Oncol Skin Cancer (T Ito, Section Editor) Melanoma is one of the deadliest malignancies. Its incidence has been significantly increasing in most countries in recent decades. Acral melanoma (AM), a peculiar subgroup of melanoma occurring on the palms, soles, and nails, is the main subtype of melanoma in people of color and is extremely rare in Caucasians. Although great progress has been made in melanoma treatment in recent years, patients with AM have shown limited benefit from current therapies and thus consequently have worse overall survival rates. Achieving durable therapeutic responses in this high-risk melanoma subtype represents one of the greatest challenges in the field. The frequency of BRAF mutations in AM is much lower than that in cutaneous melanoma, which prevents most AM patients from receiving treatment with BRAF inhibitors. However, AM has more frequent mutations such as KIT and CDK4/6, so targeted therapy may still improve the survival of some AM patients in the future. AM may be less susceptible to immune checkpoint inhibitors because of the poor immunogenicity. Therefore, how to enhance the immune response to the tumor cells may be the key to the application of immune checkpoint inhibitors in advanced AM. Anti-angiogenic drugs, albumin paclitaxel, or interferons are thought to enhance the effectiveness of immune checkpoint inhibitors. Combination therapies based on the backbone of PD-1 are more likely to provide greater clinical benefits. Understanding the molecular landscapes and immune microenvironment of AM will help optimize our combinatory strategies. Springer US 2022-09-20 2022 /pmc/articles/PMC9526689/ /pubmed/36125617 http://dx.doi.org/10.1007/s11864-022-01007-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Skin Cancer (T Ito, Section Editor) Zhang, Yiqun Lan, Shijie Wu, Di Advanced Acral Melanoma Therapies: Current Status and Future Directions |
title | Advanced Acral Melanoma Therapies: Current Status and Future Directions |
title_full | Advanced Acral Melanoma Therapies: Current Status and Future Directions |
title_fullStr | Advanced Acral Melanoma Therapies: Current Status and Future Directions |
title_full_unstemmed | Advanced Acral Melanoma Therapies: Current Status and Future Directions |
title_short | Advanced Acral Melanoma Therapies: Current Status and Future Directions |
title_sort | advanced acral melanoma therapies: current status and future directions |
topic | Skin Cancer (T Ito, Section Editor) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526689/ https://www.ncbi.nlm.nih.gov/pubmed/36125617 http://dx.doi.org/10.1007/s11864-022-01007-6 |
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