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Insights into the Molecular Mechanisms Behind Intralesional Immunotherapies for Advanced Melanoma

The incidence of cutaneous melanoma, a highly malignant skin cancer, is increasing yearly. While surgical removal of the tumor is the mainstay of treatment for patients with locally confined disease, those with metastases face uncertainty when it comes to their treatment. As melanoma is a relatively...

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Autores principales: Vidovic, Dejan, Giacomantonio, Carman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281646/
https://www.ncbi.nlm.nih.gov/pubmed/32455916
http://dx.doi.org/10.3390/cancers12051321
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author Vidovic, Dejan
Giacomantonio, Carman
author_facet Vidovic, Dejan
Giacomantonio, Carman
author_sort Vidovic, Dejan
collection PubMed
description The incidence of cutaneous melanoma, a highly malignant skin cancer, is increasing yearly. While surgical removal of the tumor is the mainstay of treatment for patients with locally confined disease, those with metastases face uncertainty when it comes to their treatment. As melanoma is a relatively immunogenic cancer, current guidelines suggest using immunotherapies that can rewire the host immune response to target melanoma tumor cells. Intralesional therapy, where immunomodulatory agents are injected directly into the tumor, are an emerging aspect of treatment for in-transit melanoma because of their ability to mitigate severe off-target immune-related adverse events. However, their immunomodulatory mechanisms are poorly understood. In this review, we will summarize and discuss the different intralesional therapies for metastatic melanoma with respect to their clinical outcomes and immune molecular mechanisms.
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spelling pubmed-72816462020-06-17 Insights into the Molecular Mechanisms Behind Intralesional Immunotherapies for Advanced Melanoma Vidovic, Dejan Giacomantonio, Carman Cancers (Basel) Review The incidence of cutaneous melanoma, a highly malignant skin cancer, is increasing yearly. While surgical removal of the tumor is the mainstay of treatment for patients with locally confined disease, those with metastases face uncertainty when it comes to their treatment. As melanoma is a relatively immunogenic cancer, current guidelines suggest using immunotherapies that can rewire the host immune response to target melanoma tumor cells. Intralesional therapy, where immunomodulatory agents are injected directly into the tumor, are an emerging aspect of treatment for in-transit melanoma because of their ability to mitigate severe off-target immune-related adverse events. However, their immunomodulatory mechanisms are poorly understood. In this review, we will summarize and discuss the different intralesional therapies for metastatic melanoma with respect to their clinical outcomes and immune molecular mechanisms. MDPI 2020-05-22 /pmc/articles/PMC7281646/ /pubmed/32455916 http://dx.doi.org/10.3390/cancers12051321 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Vidovic, Dejan
Giacomantonio, Carman
Insights into the Molecular Mechanisms Behind Intralesional Immunotherapies for Advanced Melanoma
title Insights into the Molecular Mechanisms Behind Intralesional Immunotherapies for Advanced Melanoma
title_full Insights into the Molecular Mechanisms Behind Intralesional Immunotherapies for Advanced Melanoma
title_fullStr Insights into the Molecular Mechanisms Behind Intralesional Immunotherapies for Advanced Melanoma
title_full_unstemmed Insights into the Molecular Mechanisms Behind Intralesional Immunotherapies for Advanced Melanoma
title_short Insights into the Molecular Mechanisms Behind Intralesional Immunotherapies for Advanced Melanoma
title_sort insights into the molecular mechanisms behind intralesional immunotherapies for advanced melanoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281646/
https://www.ncbi.nlm.nih.gov/pubmed/32455916
http://dx.doi.org/10.3390/cancers12051321
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