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Perspectives in melanoma: Meeting report from the Melanoma Bridge (30 November–2 December, 2017, Naples, Italy)

Metastatic melanoma represents a challenging clinical situation and, until relatively recently, there was an absence of effective treatment options. However, in 2011, the advanced melanoma treatment landscape was revolutionised with the approval of the anti-cytotoxic T-lymphocyte-associated protein-...

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Autores principales: Ascierto, Paolo A., Puzanov, Igor, Agarwala, Sanjiv S., Bifulco, Carlo, Botti, Gerardo, Caracò, Corrado, Ciliberto, Gennaro, Davies, Michael A., Dummer, Reinhard, Ferrone, Soldano, Gajewski, Thomas F., Garbe, Claus, Luke, Jason J., Marincola, Francesco M., Masucci, Giuseppe, Mehnert, Janice M., Mozzillo, Nicola, Palmieri, Giuseppe, Postow, Michael A., Schoenberger, Stephen P., Wang, Ena, Thurin, Magdalena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054754/
https://www.ncbi.nlm.nih.gov/pubmed/30031393
http://dx.doi.org/10.1186/s12967-018-1568-6
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author Ascierto, Paolo A.
Puzanov, Igor
Agarwala, Sanjiv S.
Bifulco, Carlo
Botti, Gerardo
Caracò, Corrado
Ciliberto, Gennaro
Davies, Michael A.
Dummer, Reinhard
Ferrone, Soldano
Gajewski, Thomas F.
Garbe, Claus
Luke, Jason J.
Marincola, Francesco M.
Masucci, Giuseppe
Mehnert, Janice M.
Mozzillo, Nicola
Palmieri, Giuseppe
Postow, Michael A.
Schoenberger, Stephen P.
Wang, Ena
Thurin, Magdalena
author_facet Ascierto, Paolo A.
Puzanov, Igor
Agarwala, Sanjiv S.
Bifulco, Carlo
Botti, Gerardo
Caracò, Corrado
Ciliberto, Gennaro
Davies, Michael A.
Dummer, Reinhard
Ferrone, Soldano
Gajewski, Thomas F.
Garbe, Claus
Luke, Jason J.
Marincola, Francesco M.
Masucci, Giuseppe
Mehnert, Janice M.
Mozzillo, Nicola
Palmieri, Giuseppe
Postow, Michael A.
Schoenberger, Stephen P.
Wang, Ena
Thurin, Magdalena
author_sort Ascierto, Paolo A.
collection PubMed
description Metastatic melanoma represents a challenging clinical situation and, until relatively recently, there was an absence of effective treatment options. However, in 2011, the advanced melanoma treatment landscape was revolutionised with the approval of the anti-cytotoxic T-lymphocyte-associated protein-4 checkpoint inhibitor ipilimumab and the selective BRAF kinase inhibitor vemurafenib, both of which significantly improved overall survival. Since then, availability of new immunotherapies, especially the anti-programmed death-1 checkpoint inhibitors, as well as other targeted therapies, have further improved outcomes for patients with advanced melanoma. Seven years on from the first approval of these novel therapies, evidence for the use of various immune-based and targeted approaches is continuing to increase at a rapid rate. Improved understanding of the tumour microenvironment and tumour immuno-evasion strategies has resulted in different approaches to target and harness the immune response. These new immune-based approaches offer the opportunity for various approaches with distinct modes of action being used in combination with one another, as well as combined with other treatment modalities such as targeted therapy, electrochemotherapy and surgery. The increasing number of treatment options that are now available has resulted in a growing need to identify which patients will derive most benefit from which treatments. Much research is now focused on the identification of biomarkers that can be utilised to help select patients for treatment. These and other recent advances in the management of melanoma were the focus of discussions at the third Melanoma Bridge meeting (30 November–2 December, 2017, Naples, Italy), which is summarised in this report.
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spelling pubmed-60547542018-07-23 Perspectives in melanoma: Meeting report from the Melanoma Bridge (30 November–2 December, 2017, Naples, Italy) Ascierto, Paolo A. Puzanov, Igor Agarwala, Sanjiv S. Bifulco, Carlo Botti, Gerardo Caracò, Corrado Ciliberto, Gennaro Davies, Michael A. Dummer, Reinhard Ferrone, Soldano Gajewski, Thomas F. Garbe, Claus Luke, Jason J. Marincola, Francesco M. Masucci, Giuseppe Mehnert, Janice M. Mozzillo, Nicola Palmieri, Giuseppe Postow, Michael A. Schoenberger, Stephen P. Wang, Ena Thurin, Magdalena J Transl Med Meeting Report Metastatic melanoma represents a challenging clinical situation and, until relatively recently, there was an absence of effective treatment options. However, in 2011, the advanced melanoma treatment landscape was revolutionised with the approval of the anti-cytotoxic T-lymphocyte-associated protein-4 checkpoint inhibitor ipilimumab and the selective BRAF kinase inhibitor vemurafenib, both of which significantly improved overall survival. Since then, availability of new immunotherapies, especially the anti-programmed death-1 checkpoint inhibitors, as well as other targeted therapies, have further improved outcomes for patients with advanced melanoma. Seven years on from the first approval of these novel therapies, evidence for the use of various immune-based and targeted approaches is continuing to increase at a rapid rate. Improved understanding of the tumour microenvironment and tumour immuno-evasion strategies has resulted in different approaches to target and harness the immune response. These new immune-based approaches offer the opportunity for various approaches with distinct modes of action being used in combination with one another, as well as combined with other treatment modalities such as targeted therapy, electrochemotherapy and surgery. The increasing number of treatment options that are now available has resulted in a growing need to identify which patients will derive most benefit from which treatments. Much research is now focused on the identification of biomarkers that can be utilised to help select patients for treatment. These and other recent advances in the management of melanoma were the focus of discussions at the third Melanoma Bridge meeting (30 November–2 December, 2017, Naples, Italy), which is summarised in this report. BioMed Central 2018-07-21 /pmc/articles/PMC6054754/ /pubmed/30031393 http://dx.doi.org/10.1186/s12967-018-1568-6 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Meeting Report
Ascierto, Paolo A.
Puzanov, Igor
Agarwala, Sanjiv S.
Bifulco, Carlo
Botti, Gerardo
Caracò, Corrado
Ciliberto, Gennaro
Davies, Michael A.
Dummer, Reinhard
Ferrone, Soldano
Gajewski, Thomas F.
Garbe, Claus
Luke, Jason J.
Marincola, Francesco M.
Masucci, Giuseppe
Mehnert, Janice M.
Mozzillo, Nicola
Palmieri, Giuseppe
Postow, Michael A.
Schoenberger, Stephen P.
Wang, Ena
Thurin, Magdalena
Perspectives in melanoma: Meeting report from the Melanoma Bridge (30 November–2 December, 2017, Naples, Italy)
title Perspectives in melanoma: Meeting report from the Melanoma Bridge (30 November–2 December, 2017, Naples, Italy)
title_full Perspectives in melanoma: Meeting report from the Melanoma Bridge (30 November–2 December, 2017, Naples, Italy)
title_fullStr Perspectives in melanoma: Meeting report from the Melanoma Bridge (30 November–2 December, 2017, Naples, Italy)
title_full_unstemmed Perspectives in melanoma: Meeting report from the Melanoma Bridge (30 November–2 December, 2017, Naples, Italy)
title_short Perspectives in melanoma: Meeting report from the Melanoma Bridge (30 November–2 December, 2017, Naples, Italy)
title_sort perspectives in melanoma: meeting report from the melanoma bridge (30 november–2 december, 2017, naples, italy)
topic Meeting Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054754/
https://www.ncbi.nlm.nih.gov/pubmed/30031393
http://dx.doi.org/10.1186/s12967-018-1568-6
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