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Updates on the Systemic Treatment of Advanced Non-melanoma Skin Cancer

Non-melanoma skin cancers (NMSCs), which represent a diverse group of cutaneous malignancies, are the most common forms of human neoplasia. The incidence of these diseases is increasing due to a number of factors, including that of increasing human lifespans. The majority of NMSCs are basal cell car...

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Autores principales: Tanese, Keiji, Nakamura, Yoshio, Hirai, Ikuko, Funakoshi, Takeru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635480/
https://www.ncbi.nlm.nih.gov/pubmed/31355203
http://dx.doi.org/10.3389/fmed.2019.00160
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author Tanese, Keiji
Nakamura, Yoshio
Hirai, Ikuko
Funakoshi, Takeru
author_facet Tanese, Keiji
Nakamura, Yoshio
Hirai, Ikuko
Funakoshi, Takeru
author_sort Tanese, Keiji
collection PubMed
description Non-melanoma skin cancers (NMSCs), which represent a diverse group of cutaneous malignancies, are the most common forms of human neoplasia. The incidence of these diseases is increasing due to a number of factors, including that of increasing human lifespans. The majority of NMSCs are basal cell carcinomas (BCC) and cutaneous squamous cell carcinomas (cSCC), with the remainder being various rare skin cancers, including extramammary Paget's disease (EMPD), Merkel cell carcinoma (MCC), and several skin adnexal carcinomas. Of these, MCC usually shows aggressive behavior with a high mortality rate. On the other hand, BCC, cSCC, EMPD, and skin adnexal tumors usually show an indolent clinical course and metastasize only rarely. Nevertheless, the metastatic forms of these tumors commonly lead to poor patient outcome. A definitive management strategy for the treatment of advanced NMSC has not been established, mainly due to their rarity and lack of reliable information based on well-controlled randomized trials. Chemotherapeutic regimens for treatment of these diseases have been mainly based on the observations of isolated, small case series or clinical trials with a limited numbers of patients. However, accumulating evidence regarding their pathobiological backgrounds as well as recent advances in molecular biotechnology have facilitated the development of novel drugs for treatment of these diseases. Over the past decade, the U.S. Food and Drug Administration has approved several molecular targeting therapies, including Hedgehog inhibitors for BCC, monoclonal antibodies targeting anti-programmed death ligand-1 and anti- programmed cell death 1 (PD-1) for MCC, and anti-PD-1 for cSCC. Here, we review their clinical utility and discuss updated systemic treatment strategies for advanced NMSC.
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spelling pubmed-66354802019-07-26 Updates on the Systemic Treatment of Advanced Non-melanoma Skin Cancer Tanese, Keiji Nakamura, Yoshio Hirai, Ikuko Funakoshi, Takeru Front Med (Lausanne) Medicine Non-melanoma skin cancers (NMSCs), which represent a diverse group of cutaneous malignancies, are the most common forms of human neoplasia. The incidence of these diseases is increasing due to a number of factors, including that of increasing human lifespans. The majority of NMSCs are basal cell carcinomas (BCC) and cutaneous squamous cell carcinomas (cSCC), with the remainder being various rare skin cancers, including extramammary Paget's disease (EMPD), Merkel cell carcinoma (MCC), and several skin adnexal carcinomas. Of these, MCC usually shows aggressive behavior with a high mortality rate. On the other hand, BCC, cSCC, EMPD, and skin adnexal tumors usually show an indolent clinical course and metastasize only rarely. Nevertheless, the metastatic forms of these tumors commonly lead to poor patient outcome. A definitive management strategy for the treatment of advanced NMSC has not been established, mainly due to their rarity and lack of reliable information based on well-controlled randomized trials. Chemotherapeutic regimens for treatment of these diseases have been mainly based on the observations of isolated, small case series or clinical trials with a limited numbers of patients. However, accumulating evidence regarding their pathobiological backgrounds as well as recent advances in molecular biotechnology have facilitated the development of novel drugs for treatment of these diseases. Over the past decade, the U.S. Food and Drug Administration has approved several molecular targeting therapies, including Hedgehog inhibitors for BCC, monoclonal antibodies targeting anti-programmed death ligand-1 and anti- programmed cell death 1 (PD-1) for MCC, and anti-PD-1 for cSCC. Here, we review their clinical utility and discuss updated systemic treatment strategies for advanced NMSC. Frontiers Media S.A. 2019-07-10 /pmc/articles/PMC6635480/ /pubmed/31355203 http://dx.doi.org/10.3389/fmed.2019.00160 Text en Copyright © 2019 Tanese, Nakamura, Hirai and Funakoshi. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Tanese, Keiji
Nakamura, Yoshio
Hirai, Ikuko
Funakoshi, Takeru
Updates on the Systemic Treatment of Advanced Non-melanoma Skin Cancer
title Updates on the Systemic Treatment of Advanced Non-melanoma Skin Cancer
title_full Updates on the Systemic Treatment of Advanced Non-melanoma Skin Cancer
title_fullStr Updates on the Systemic Treatment of Advanced Non-melanoma Skin Cancer
title_full_unstemmed Updates on the Systemic Treatment of Advanced Non-melanoma Skin Cancer
title_short Updates on the Systemic Treatment of Advanced Non-melanoma Skin Cancer
title_sort updates on the systemic treatment of advanced non-melanoma skin cancer
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635480/
https://www.ncbi.nlm.nih.gov/pubmed/31355203
http://dx.doi.org/10.3389/fmed.2019.00160
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