Cargando…

The biology and treatment of Merkel cell carcinoma: current understanding and research priorities

Merkel cell carcinoma (MCC) is a rare and aggressive skin cancer associated with advanced age and immunosuppression. Over the past decade, an association has been discovered between MCC and either integration of the Merkel cell polyomavirus, which likely drives tumorigenesis, or somatic mutations ow...

Descripción completa

Detalles Bibliográficos
Autores principales: Harms, Paul W., Harms, Kelly L., Moore, Patrick S., DeCaprio, James A., Nghiem, Paul, Wong, Michael K. K., Brownell, Isaac
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319370/
https://www.ncbi.nlm.nih.gov/pubmed/30287935
http://dx.doi.org/10.1038/s41571-018-0103-2
_version_ 1783385058012299264
author Harms, Paul W.
Harms, Kelly L.
Moore, Patrick S.
DeCaprio, James A.
Nghiem, Paul
Wong, Michael K. K.
Brownell, Isaac
author_facet Harms, Paul W.
Harms, Kelly L.
Moore, Patrick S.
DeCaprio, James A.
Nghiem, Paul
Wong, Michael K. K.
Brownell, Isaac
author_sort Harms, Paul W.
collection PubMed
description Merkel cell carcinoma (MCC) is a rare and aggressive skin cancer associated with advanced age and immunosuppression. Over the past decade, an association has been discovered between MCC and either integration of the Merkel cell polyomavirus, which likely drives tumorigenesis, or somatic mutations owing to ultraviolet-induced DNA damage. Both virus-positive and virus-negative MCCs are immunogenic, and inhibition of the programmed cell death protein 1 (PD-1)–programmed cell death 1 ligand 1 (PD-L1) immune checkpoint has proved to be highly effective in treating patients with metastatic MCC; however, not all patients have a durable response to immunotherapy. Despite these rapid advances in the understanding and management of patients with MCC, many basic, translational and clinical research questions remain unanswered. In March 2018, an International Workshop on Merkel Cell Carcinoma Research was held at the US National Cancer Institute, at which academic, government and industry experts met to identify the highest-priority research questions. Here, we review the biology and treatment of MCC and report the consensus-based recommendations agreed upon during the workshop.
format Online
Article
Text
id pubmed-6319370
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-63193702019-06-01 The biology and treatment of Merkel cell carcinoma: current understanding and research priorities Harms, Paul W. Harms, Kelly L. Moore, Patrick S. DeCaprio, James A. Nghiem, Paul Wong, Michael K. K. Brownell, Isaac Nat Rev Clin Oncol Consensus Statement Merkel cell carcinoma (MCC) is a rare and aggressive skin cancer associated with advanced age and immunosuppression. Over the past decade, an association has been discovered between MCC and either integration of the Merkel cell polyomavirus, which likely drives tumorigenesis, or somatic mutations owing to ultraviolet-induced DNA damage. Both virus-positive and virus-negative MCCs are immunogenic, and inhibition of the programmed cell death protein 1 (PD-1)–programmed cell death 1 ligand 1 (PD-L1) immune checkpoint has proved to be highly effective in treating patients with metastatic MCC; however, not all patients have a durable response to immunotherapy. Despite these rapid advances in the understanding and management of patients with MCC, many basic, translational and clinical research questions remain unanswered. In March 2018, an International Workshop on Merkel Cell Carcinoma Research was held at the US National Cancer Institute, at which academic, government and industry experts met to identify the highest-priority research questions. Here, we review the biology and treatment of MCC and report the consensus-based recommendations agreed upon during the workshop. Nature Publishing Group UK 2018-10-04 2018 /pmc/articles/PMC6319370/ /pubmed/30287935 http://dx.doi.org/10.1038/s41571-018-0103-2 Text en © Springer Nature Limited 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Consensus Statement
Harms, Paul W.
Harms, Kelly L.
Moore, Patrick S.
DeCaprio, James A.
Nghiem, Paul
Wong, Michael K. K.
Brownell, Isaac
The biology and treatment of Merkel cell carcinoma: current understanding and research priorities
title The biology and treatment of Merkel cell carcinoma: current understanding and research priorities
title_full The biology and treatment of Merkel cell carcinoma: current understanding and research priorities
title_fullStr The biology and treatment of Merkel cell carcinoma: current understanding and research priorities
title_full_unstemmed The biology and treatment of Merkel cell carcinoma: current understanding and research priorities
title_short The biology and treatment of Merkel cell carcinoma: current understanding and research priorities
title_sort biology and treatment of merkel cell carcinoma: current understanding and research priorities
topic Consensus Statement
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319370/
https://www.ncbi.nlm.nih.gov/pubmed/30287935
http://dx.doi.org/10.1038/s41571-018-0103-2
work_keys_str_mv AT harmspaulw thebiologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT harmskellyl thebiologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT moorepatricks thebiologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT decapriojamesa thebiologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT nghiempaul thebiologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT wongmichaelkk thebiologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT brownellisaac thebiologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT thebiologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT harmspaulw biologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT harmskellyl biologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT moorepatricks biologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT decapriojamesa biologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT nghiempaul biologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT wongmichaelkk biologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT brownellisaac biologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities
AT biologyandtreatmentofmerkelcellcarcinomacurrentunderstandingandresearchpriorities