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Perspectives in Melanoma: meeting report from the Melanoma Bridge (December 2nd – 4th, 2021, Italy)

Advances in immune checkpoint and combination therapy have led to improvement in overall survival for patients with advanced melanoma. Improved understanding of the tumor, tumor microenvironment and tumor immune-evasion mechanisms has resulted in new approaches to targeting and harnessing the host i...

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Autores principales: Ascierto, Paolo A., Agarwala, Sanjiv S., Blank, Christian, Caracò, Corrado, Carvajal, Richard D., Ernstoff, Marc S., Ferrone, Soldano, Fox, Bernard A., Gajewski, Thomas F., Garbe, Claus, Grob, Jean-Jacques, Hamid, Omid, Krogsgaard, Michelle, Lo, Roger S., Lund, Amanda W., Madonna, Gabriele, Michielin, Olivier, Neyns, Bart, Osman, Iman, Peters, Solange, Poulikakos, Poulikos I., Quezada, Sergio A., Reinfeld, Bradley, Zitvogel, Laurence, Puzanov, Igor, Thurin, Magdalena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440864/
https://www.ncbi.nlm.nih.gov/pubmed/36058945
http://dx.doi.org/10.1186/s12967-022-03592-4
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author Ascierto, Paolo A.
Agarwala, Sanjiv S.
Blank, Christian
Caracò, Corrado
Carvajal, Richard D.
Ernstoff, Marc S.
Ferrone, Soldano
Fox, Bernard A.
Gajewski, Thomas F.
Garbe, Claus
Grob, Jean-Jacques
Hamid, Omid
Krogsgaard, Michelle
Lo, Roger S.
Lund, Amanda W.
Madonna, Gabriele
Michielin, Olivier
Neyns, Bart
Osman, Iman
Peters, Solange
Poulikakos, Poulikos I.
Quezada, Sergio A.
Reinfeld, Bradley
Zitvogel, Laurence
Puzanov, Igor
Thurin, Magdalena
author_facet Ascierto, Paolo A.
Agarwala, Sanjiv S.
Blank, Christian
Caracò, Corrado
Carvajal, Richard D.
Ernstoff, Marc S.
Ferrone, Soldano
Fox, Bernard A.
Gajewski, Thomas F.
Garbe, Claus
Grob, Jean-Jacques
Hamid, Omid
Krogsgaard, Michelle
Lo, Roger S.
Lund, Amanda W.
Madonna, Gabriele
Michielin, Olivier
Neyns, Bart
Osman, Iman
Peters, Solange
Poulikakos, Poulikos I.
Quezada, Sergio A.
Reinfeld, Bradley
Zitvogel, Laurence
Puzanov, Igor
Thurin, Magdalena
author_sort Ascierto, Paolo A.
collection PubMed
description Advances in immune checkpoint and combination therapy have led to improvement in overall survival for patients with advanced melanoma. Improved understanding of the tumor, tumor microenvironment and tumor immune-evasion mechanisms has resulted in new approaches to targeting and harnessing the host immune response. Combination modalities with other immunotherapy agents, chemotherapy, radiotherapy, electrochemotherapy are also being explored to overcome resistance and to potentiate the immune response. In addition, novel approaches such as adoptive cell therapy, oncogenic viruses, vaccines and different strategies of drug administration including sequential, or combination treatment are being tested. Despite the progress in diagnosis of melanocytic lesions, correct classification of patients, selection of appropriate adjuvant and systemic theràapies, and prediction of response to therapy remain real challenges in melanoma. Improved understanding of the tumor microenvironment, tumor immunity and response to therapy has prompted extensive translational and clinical research in melanoma. There is a growing evidence that genomic and immune features of pre-treatment tumor biopsies may correlate with response in patients with melanoma and other cancers, but they have yet to be fully characterized and implemented clinically. Development of novel biomarker platforms may help to improve diagnostics and predictive accuracy for selection of patients for specific treatment. Overall, the future research efforts in melanoma therapeutics and translational research should focus on several aspects including: (a) developing robust biomarkers to predict efficacy of therapeutic modalities to guide clinical decision-making and optimize treatment regimens, (b) identifying mechanisms of therapeutic resistance to immune checkpoint inhibitors that are potentially actionable, (c) identifying biomarkers to predict therapy-induced adverse events, and (d) studying mechanism of actions of therapeutic agents and developing algorithms to optimize combination treatments. During the Melanoma Bridge meeting (December 2nd-4th, 2021, Naples, Italy) discussions focused on the currently approved systemic and local therapies for advanced melanoma and discussed novel biomarker strategies and advances in precision medicine as well as the impact of COVID-19 pandemic on management of melanoma patients.
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spelling pubmed-94408642022-09-05 Perspectives in Melanoma: meeting report from the Melanoma Bridge (December 2nd – 4th, 2021, Italy) Ascierto, Paolo A. Agarwala, Sanjiv S. Blank, Christian Caracò, Corrado Carvajal, Richard D. Ernstoff, Marc S. Ferrone, Soldano Fox, Bernard A. Gajewski, Thomas F. Garbe, Claus Grob, Jean-Jacques Hamid, Omid Krogsgaard, Michelle Lo, Roger S. Lund, Amanda W. Madonna, Gabriele Michielin, Olivier Neyns, Bart Osman, Iman Peters, Solange Poulikakos, Poulikos I. Quezada, Sergio A. Reinfeld, Bradley Zitvogel, Laurence Puzanov, Igor Thurin, Magdalena J Transl Med Meeting Report Advances in immune checkpoint and combination therapy have led to improvement in overall survival for patients with advanced melanoma. Improved understanding of the tumor, tumor microenvironment and tumor immune-evasion mechanisms has resulted in new approaches to targeting and harnessing the host immune response. Combination modalities with other immunotherapy agents, chemotherapy, radiotherapy, electrochemotherapy are also being explored to overcome resistance and to potentiate the immune response. In addition, novel approaches such as adoptive cell therapy, oncogenic viruses, vaccines and different strategies of drug administration including sequential, or combination treatment are being tested. Despite the progress in diagnosis of melanocytic lesions, correct classification of patients, selection of appropriate adjuvant and systemic theràapies, and prediction of response to therapy remain real challenges in melanoma. Improved understanding of the tumor microenvironment, tumor immunity and response to therapy has prompted extensive translational and clinical research in melanoma. There is a growing evidence that genomic and immune features of pre-treatment tumor biopsies may correlate with response in patients with melanoma and other cancers, but they have yet to be fully characterized and implemented clinically. Development of novel biomarker platforms may help to improve diagnostics and predictive accuracy for selection of patients for specific treatment. Overall, the future research efforts in melanoma therapeutics and translational research should focus on several aspects including: (a) developing robust biomarkers to predict efficacy of therapeutic modalities to guide clinical decision-making and optimize treatment regimens, (b) identifying mechanisms of therapeutic resistance to immune checkpoint inhibitors that are potentially actionable, (c) identifying biomarkers to predict therapy-induced adverse events, and (d) studying mechanism of actions of therapeutic agents and developing algorithms to optimize combination treatments. During the Melanoma Bridge meeting (December 2nd-4th, 2021, Naples, Italy) discussions focused on the currently approved systemic and local therapies for advanced melanoma and discussed novel biomarker strategies and advances in precision medicine as well as the impact of COVID-19 pandemic on management of melanoma patients. BioMed Central 2022-09-04 /pmc/articles/PMC9440864/ /pubmed/36058945 http://dx.doi.org/10.1186/s12967-022-03592-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Meeting Report
Ascierto, Paolo A.
Agarwala, Sanjiv S.
Blank, Christian
Caracò, Corrado
Carvajal, Richard D.
Ernstoff, Marc S.
Ferrone, Soldano
Fox, Bernard A.
Gajewski, Thomas F.
Garbe, Claus
Grob, Jean-Jacques
Hamid, Omid
Krogsgaard, Michelle
Lo, Roger S.
Lund, Amanda W.
Madonna, Gabriele
Michielin, Olivier
Neyns, Bart
Osman, Iman
Peters, Solange
Poulikakos, Poulikos I.
Quezada, Sergio A.
Reinfeld, Bradley
Zitvogel, Laurence
Puzanov, Igor
Thurin, Magdalena
Perspectives in Melanoma: meeting report from the Melanoma Bridge (December 2nd – 4th, 2021, Italy)
title Perspectives in Melanoma: meeting report from the Melanoma Bridge (December 2nd – 4th, 2021, Italy)
title_full Perspectives in Melanoma: meeting report from the Melanoma Bridge (December 2nd – 4th, 2021, Italy)
title_fullStr Perspectives in Melanoma: meeting report from the Melanoma Bridge (December 2nd – 4th, 2021, Italy)
title_full_unstemmed Perspectives in Melanoma: meeting report from the Melanoma Bridge (December 2nd – 4th, 2021, Italy)
title_short Perspectives in Melanoma: meeting report from the Melanoma Bridge (December 2nd – 4th, 2021, Italy)
title_sort perspectives in melanoma: meeting report from the melanoma bridge (december 2nd – 4th, 2021, italy)
topic Meeting Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440864/
https://www.ncbi.nlm.nih.gov/pubmed/36058945
http://dx.doi.org/10.1186/s12967-022-03592-4
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