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

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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; International Workshop on Merkel Cell Carcinoma Research (IWMCC) Working Group.

In: NAT REV CLIN ONCOL, Vol. 15, No. 12, 12.2018, p. 763–776.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

Harvard

Harms, PW, Harms, KL, Moore, PS, DeCaprio, JA, Nghiem, P, Wong, MKK, Brownell, I & International Workshop on Merkel Cell Carcinoma Research (IWMCC) Working Group 2018, 'The biology and treatment of Merkel cell carcinoma:current understanding and research priorities', NAT REV CLIN ONCOL, vol. 15, no. 12, pp. 763–776. https://doi.org/10.1038/s41571-018-0103-2

APA

Harms, P. W., Harms, K. L., Moore, P. S., DeCaprio, J. A., Nghiem, P., Wong, M. K. K., Brownell, I., & International Workshop on Merkel Cell Carcinoma Research (IWMCC) Working Group (2018). The biology and treatment of Merkel cell carcinoma:current understanding and research priorities. NAT REV CLIN ONCOL, 15(12), 763–776. https://doi.org/10.1038/s41571-018-0103-2

Vancouver

Bibtex

@article{a379ba048e7d4485827298044eb04815,
title = "The biology and treatment of Merkel cell carcinoma:current understanding and research priorities",
abstract = "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.",
keywords = "Journal Article, Review",
author = "Harms, {Paul W} and Harms, {Kelly L} and Moore, {Patrick S} and DeCaprio, {James A} and Paul Nghiem and Wong, {Michael K K} and Isaac Brownell and {International Workshop on Merkel Cell Carcinoma Research (IWMCC) Working Group}",
year = "2018",
month = dec,
doi = "10.1038/s41571-018-0103-2",
language = "English",
volume = "15",
pages = "763–776",
journal = "NAT REV CLIN ONCOL",
issn = "1759-4774",
publisher = "NATURE PUBLISHING GROUP",
number = "12",

}

RIS

TY - JOUR

T1 - The biology and treatment of Merkel cell carcinoma:current understanding and research priorities

AU - Harms, Paul W

AU - Harms, Kelly L

AU - Moore, Patrick S

AU - DeCaprio, James A

AU - Nghiem, Paul

AU - Wong, Michael K K

AU - Brownell, Isaac

AU - International Workshop on Merkel Cell Carcinoma Research (IWMCC) Working Group

PY - 2018/12

Y1 - 2018/12

N2 - 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.

AB - 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.

KW - Journal Article

KW - Review

U2 - 10.1038/s41571-018-0103-2

DO - 10.1038/s41571-018-0103-2

M3 - SCORING: Review article

C2 - 30287935

VL - 15

SP - 763

EP - 776

JO - NAT REV CLIN ONCOL

JF - NAT REV CLIN ONCOL

SN - 1759-4774

IS - 12

ER -