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Vismodegib: the Proof of Concept in Basal Cell Carcinoma
Although basal cell carcinoma (BCC) is the most common cancer worldwide, its metastatic dissemination is exceptional. Before 2012, we had a few treatment options available for metastatic or locally advanced cases. Management of these patients was complicated due to the lack of scientific data, the d...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051803/ https://www.ncbi.nlm.nih.gov/pubmed/24932107 http://dx.doi.org/10.4137/CMO.S14569 |
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author | Berrada, Narjiss Lkhoyali, Siham Mrabti, Hind Errihani, Hassan |
author_facet | Berrada, Narjiss Lkhoyali, Siham Mrabti, Hind Errihani, Hassan |
author_sort | Berrada, Narjiss |
collection | PubMed |
description | Although basal cell carcinoma (BCC) is the most common cancer worldwide, its metastatic dissemination is exceptional. Before 2012, we had a few treatment options available for metastatic or locally advanced cases. Management of these patients was complicated due to the lack of scientific data, the deterioration of a patient’s general status, the patient’s advanced age, and the presence of multiple comorbidities. The hedgehog signaling pathway is dysregulated in BCC. The exploration of this signaling pathway yielded to a major milestone in the treatment of advanced BCC. Vismodegib (GDC-0449), an oral small-molecule agent that targets the Hedgehog signaling pathway, demonstrates high levels of activity in clinical trials. It was approved in January 2012 for the treatment of locally advanced or metastatic BCC. Vismodegib confirms, once again, the interest in exploring the signal transduction pathways in cancers. |
format | Online Article Text |
id | pubmed-4051803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-40518032014-06-13 Vismodegib: the Proof of Concept in Basal Cell Carcinoma Berrada, Narjiss Lkhoyali, Siham Mrabti, Hind Errihani, Hassan Clin Med Insights Oncol Short Review Although basal cell carcinoma (BCC) is the most common cancer worldwide, its metastatic dissemination is exceptional. Before 2012, we had a few treatment options available for metastatic or locally advanced cases. Management of these patients was complicated due to the lack of scientific data, the deterioration of a patient’s general status, the patient’s advanced age, and the presence of multiple comorbidities. The hedgehog signaling pathway is dysregulated in BCC. The exploration of this signaling pathway yielded to a major milestone in the treatment of advanced BCC. Vismodegib (GDC-0449), an oral small-molecule agent that targets the Hedgehog signaling pathway, demonstrates high levels of activity in clinical trials. It was approved in January 2012 for the treatment of locally advanced or metastatic BCC. Vismodegib confirms, once again, the interest in exploring the signal transduction pathways in cancers. Libertas Academica 2014-06-02 /pmc/articles/PMC4051803/ /pubmed/24932107 http://dx.doi.org/10.4137/CMO.S14569 Text en © 2014 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article published under the Creative Commons CC-BY-NC 3.0 license. |
spellingShingle | Short Review Berrada, Narjiss Lkhoyali, Siham Mrabti, Hind Errihani, Hassan Vismodegib: the Proof of Concept in Basal Cell Carcinoma |
title | Vismodegib: the Proof of Concept in Basal Cell Carcinoma |
title_full | Vismodegib: the Proof of Concept in Basal Cell Carcinoma |
title_fullStr | Vismodegib: the Proof of Concept in Basal Cell Carcinoma |
title_full_unstemmed | Vismodegib: the Proof of Concept in Basal Cell Carcinoma |
title_short | Vismodegib: the Proof of Concept in Basal Cell Carcinoma |
title_sort | vismodegib: the proof of concept in basal cell carcinoma |
topic | Short Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051803/ https://www.ncbi.nlm.nih.gov/pubmed/24932107 http://dx.doi.org/10.4137/CMO.S14569 |
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