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EGFR inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa
Dystrophic epidermolysis bullosa (DEB) is a hereditary skin fragility disorder, characterized by trauma-induced blistering followed by soft tissue fibrosis. One of the most feared complications is the early development of aggressive cutaneous squamous cell carcinomas (SCC). For patients with locally...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889571/ https://www.ncbi.nlm.nih.gov/pubmed/31796084 http://dx.doi.org/10.1186/s13023-019-1262-7 |
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author | Diociaiuti, Andrea Steinke, Holger Nyström, Alexander Schwieger-Briel, Agnes Meiss, Frank Pfannenberg, Christina Bruckner-Tuderman, Leena Ruf, Juri De Vito, Rita El Hachem, May Kiritsi, Dimitra |
author_facet | Diociaiuti, Andrea Steinke, Holger Nyström, Alexander Schwieger-Briel, Agnes Meiss, Frank Pfannenberg, Christina Bruckner-Tuderman, Leena Ruf, Juri De Vito, Rita El Hachem, May Kiritsi, Dimitra |
author_sort | Diociaiuti, Andrea |
collection | PubMed |
description | Dystrophic epidermolysis bullosa (DEB) is a hereditary skin fragility disorder, characterized by trauma-induced blistering followed by soft tissue fibrosis. One of the most feared complications is the early development of aggressive cutaneous squamous cell carcinomas (SCC). For patients with locally advanced or metastasized SCCs treatment with cetuximab, a monoclonal antibody against epidermal growth factor receptor (EGFR), has been proposed and so far, treatment of five DEB patients with cetuximab has been published. With this report, we extend the spectrum of EB patients treated with cetuximab by adding two additional patients. Taking together all DEB cases treated with cetuximab, we propose that cetuximab should be administered as early as possible, since it seems to be more efficient and is accompanied by rather mild adverse effects. We also show that EGFR is frequently expressed in DEB-associated SCCs, although there were noticeable differences in the level of expression, which may influence responsiveness to EGFR-targeting therapies. Although only limited experiences with targeted cancer treatments in EB exist, such reports highlight the treatments’ effects in this specific cohort and assist our therapeutic decisions. |
format | Online Article Text |
id | pubmed-6889571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68895712019-12-11 EGFR inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa Diociaiuti, Andrea Steinke, Holger Nyström, Alexander Schwieger-Briel, Agnes Meiss, Frank Pfannenberg, Christina Bruckner-Tuderman, Leena Ruf, Juri De Vito, Rita El Hachem, May Kiritsi, Dimitra Orphanet J Rare Dis Letter to the Editor Dystrophic epidermolysis bullosa (DEB) is a hereditary skin fragility disorder, characterized by trauma-induced blistering followed by soft tissue fibrosis. One of the most feared complications is the early development of aggressive cutaneous squamous cell carcinomas (SCC). For patients with locally advanced or metastasized SCCs treatment with cetuximab, a monoclonal antibody against epidermal growth factor receptor (EGFR), has been proposed and so far, treatment of five DEB patients with cetuximab has been published. With this report, we extend the spectrum of EB patients treated with cetuximab by adding two additional patients. Taking together all DEB cases treated with cetuximab, we propose that cetuximab should be administered as early as possible, since it seems to be more efficient and is accompanied by rather mild adverse effects. We also show that EGFR is frequently expressed in DEB-associated SCCs, although there were noticeable differences in the level of expression, which may influence responsiveness to EGFR-targeting therapies. Although only limited experiences with targeted cancer treatments in EB exist, such reports highlight the treatments’ effects in this specific cohort and assist our therapeutic decisions. BioMed Central 2019-12-03 /pmc/articles/PMC6889571/ /pubmed/31796084 http://dx.doi.org/10.1186/s13023-019-1262-7 Text en © The Author(s). 2019 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 | Letter to the Editor Diociaiuti, Andrea Steinke, Holger Nyström, Alexander Schwieger-Briel, Agnes Meiss, Frank Pfannenberg, Christina Bruckner-Tuderman, Leena Ruf, Juri De Vito, Rita El Hachem, May Kiritsi, Dimitra EGFR inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa |
title | EGFR inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa |
title_full | EGFR inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa |
title_fullStr | EGFR inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa |
title_full_unstemmed | EGFR inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa |
title_short | EGFR inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa |
title_sort | egfr inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889571/ https://www.ncbi.nlm.nih.gov/pubmed/31796084 http://dx.doi.org/10.1186/s13023-019-1262-7 |
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