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Update of advanced cutaneous squamous cell carcinoma
The incidence of cutaneous squamous cell carcinoma (cSCC) is rapidly increasing. A growing part of this patient group is formed by immunocompromised patients, for example organ‐transplant recipients (OTR). Although over 90% of the cSCC show a relatively harmless clinical behaviour, there is also a c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299882/ https://www.ncbi.nlm.nih.gov/pubmed/34855246 http://dx.doi.org/10.1111/jdv.17728 |
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author | de Jong, E. Lammerts, M.U.P.A. Genders, R.E. Bouwes Bavinck, J.N. |
author_facet | de Jong, E. Lammerts, M.U.P.A. Genders, R.E. Bouwes Bavinck, J.N. |
author_sort | de Jong, E. |
collection | PubMed |
description | The incidence of cutaneous squamous cell carcinoma (cSCC) is rapidly increasing. A growing part of this patient group is formed by immunocompromised patients, for example organ‐transplant recipients (OTR). Although over 90% of the cSCC show a relatively harmless clinical behaviour, there is also a chance of developing advanced cSCC and metastases. Locally advanced cSCC are defined as cSCC that have locally advanced progression and are no longer amenable to surgery or radiation therapy. Better understanding of the clinical behaviour of cSCC is essential to discriminate between low‐ and high‐risk cSCC. Staging systems are important and have recently been improved. Genetic characterisation of SCC will likely become an important tool to help distinguish low and high‐risk cSCC with an increased potential to metastasise in the near future. Available treatments for high‐risk and advanced cSCC include surgery, radiotherapy, chemotherapy and targeted therapy with epidermal growth factor receptors inhibitors. Anti‐PD‐1 antibodies show promising results with response rates of up to 50% in both locally advanced and metastatic cSCC but, in its present form, is not suitable for OTR. |
format | Online Article Text |
id | pubmed-9299882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92998822022-07-21 Update of advanced cutaneous squamous cell carcinoma de Jong, E. Lammerts, M.U.P.A. Genders, R.E. Bouwes Bavinck, J.N. J Eur Acad Dermatol Venereol This supplement was supported by a grant from Sanofi‐Aventis Deutschland GmbH The incidence of cutaneous squamous cell carcinoma (cSCC) is rapidly increasing. A growing part of this patient group is formed by immunocompromised patients, for example organ‐transplant recipients (OTR). Although over 90% of the cSCC show a relatively harmless clinical behaviour, there is also a chance of developing advanced cSCC and metastases. Locally advanced cSCC are defined as cSCC that have locally advanced progression and are no longer amenable to surgery or radiation therapy. Better understanding of the clinical behaviour of cSCC is essential to discriminate between low‐ and high‐risk cSCC. Staging systems are important and have recently been improved. Genetic characterisation of SCC will likely become an important tool to help distinguish low and high‐risk cSCC with an increased potential to metastasise in the near future. Available treatments for high‐risk and advanced cSCC include surgery, radiotherapy, chemotherapy and targeted therapy with epidermal growth factor receptors inhibitors. Anti‐PD‐1 antibodies show promising results with response rates of up to 50% in both locally advanced and metastatic cSCC but, in its present form, is not suitable for OTR. John Wiley and Sons Inc. 2021-12-02 2022-01 /pmc/articles/PMC9299882/ /pubmed/34855246 http://dx.doi.org/10.1111/jdv.17728 Text en © 2021 The Authors. Journal of the European Academy of Dermatology and Venereology published by John Wiley & Sons Ltd on behalf of European Academy of Dermatology and Venereology https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | This supplement was supported by a grant from Sanofi‐Aventis Deutschland GmbH de Jong, E. Lammerts, M.U.P.A. Genders, R.E. Bouwes Bavinck, J.N. Update of advanced cutaneous squamous cell carcinoma |
title | Update of advanced cutaneous squamous cell carcinoma |
title_full | Update of advanced cutaneous squamous cell carcinoma |
title_fullStr | Update of advanced cutaneous squamous cell carcinoma |
title_full_unstemmed | Update of advanced cutaneous squamous cell carcinoma |
title_short | Update of advanced cutaneous squamous cell carcinoma |
title_sort | update of advanced cutaneous squamous cell carcinoma |
topic | This supplement was supported by a grant from Sanofi‐Aventis Deutschland GmbH |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299882/ https://www.ncbi.nlm.nih.gov/pubmed/34855246 http://dx.doi.org/10.1111/jdv.17728 |
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