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Sonidegib in the Treatment of Locally Advanced Basal Cell Carcinoma: A Retrospective Study
Sonidegib, a hedgehog pathway inhibitor, is indicated for treatment of locally advanced basal cell carcinoma, based on the results of the BOLT study. However, to date, no real-world study of sonidegib has been reported. An observational, retrospective, single-centre study (PaSoS study) was conducted...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Society for Publication of Acta Dermato-Venereologica
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574683/ https://www.ncbi.nlm.nih.gov/pubmed/35604234 http://dx.doi.org/10.2340/actadv.v102.1995 |
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author | HERMS, Florian BAROUDJIAN, Barouyr DELYON, Julie LALY, Pauline TETU, Pauline LEBBE, Céleste BASSET-SEGUIN, Nicole |
author_facet | HERMS, Florian BAROUDJIAN, Barouyr DELYON, Julie LALY, Pauline TETU, Pauline LEBBE, Céleste BASSET-SEGUIN, Nicole |
author_sort | HERMS, Florian |
collection | PubMed |
description | Sonidegib, a hedgehog pathway inhibitor, is indicated for treatment of locally advanced basal cell carcinoma, based on the results of the BOLT study. However, to date, no real-world study of sonidegib has been reported. An observational, retrospective, single-centre study (PaSoS study) was conducted. The primary objective was to evaluate the efficacy of sonidegib for treatment of locally advanced basal cell carcinoma in a real-world setting. Secondary objectives included modalities of use, tolerability, tumour evolution, and management after discontinuation. A total of 21 patients treated with sonidegib were included from March 2018 to January 2021. The median follow-up was 18.7 months and median exposure 7.0 months. Objective response (OR) rate was 81.0% (n = 17) including 6 (29%) patients with a complete response (CR). Disease control rate was 100%. First tumour response was rapid, with a median time of 2.3 months. Nine (43%) patients underwent surgery after sonidegib discontinuation, and no relapse was observed. All the patients experienced at least 1 adverse event (AE). Muscle spasms were the most frequent AE (n = 14; 67%), followed by dysgeusia (n = 8; 38%) and alopecia (n = 12; 57%). The efficacy and safety profile of sonidegib in this first-to-date real-life trial are consistent with prior results. Overall, real-world evidence corroborated sonidegib efficacy and tolerability as a first-line treatment for locally advanced basal cell carcinoma. |
format | Online Article Text |
id | pubmed-9574683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Society for Publication of Acta Dermato-Venereologica |
record_format | MEDLINE/PubMed |
spelling | pubmed-95746832022-10-20 Sonidegib in the Treatment of Locally Advanced Basal Cell Carcinoma: A Retrospective Study HERMS, Florian BAROUDJIAN, Barouyr DELYON, Julie LALY, Pauline TETU, Pauline LEBBE, Céleste BASSET-SEGUIN, Nicole Acta Derm Venereol Original Article Sonidegib, a hedgehog pathway inhibitor, is indicated for treatment of locally advanced basal cell carcinoma, based on the results of the BOLT study. However, to date, no real-world study of sonidegib has been reported. An observational, retrospective, single-centre study (PaSoS study) was conducted. The primary objective was to evaluate the efficacy of sonidegib for treatment of locally advanced basal cell carcinoma in a real-world setting. Secondary objectives included modalities of use, tolerability, tumour evolution, and management after discontinuation. A total of 21 patients treated with sonidegib were included from March 2018 to January 2021. The median follow-up was 18.7 months and median exposure 7.0 months. Objective response (OR) rate was 81.0% (n = 17) including 6 (29%) patients with a complete response (CR). Disease control rate was 100%. First tumour response was rapid, with a median time of 2.3 months. Nine (43%) patients underwent surgery after sonidegib discontinuation, and no relapse was observed. All the patients experienced at least 1 adverse event (AE). Muscle spasms were the most frequent AE (n = 14; 67%), followed by dysgeusia (n = 8; 38%) and alopecia (n = 12; 57%). The efficacy and safety profile of sonidegib in this first-to-date real-life trial are consistent with prior results. Overall, real-world evidence corroborated sonidegib efficacy and tolerability as a first-line treatment for locally advanced basal cell carcinoma. Society for Publication of Acta Dermato-Venereologica 2022-06-21 /pmc/articles/PMC9574683/ /pubmed/35604234 http://dx.doi.org/10.2340/actadv.v102.1995 Text en © 2022 Acta Dermato-Venereologica https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the CC BY-NC license |
spellingShingle | Original Article HERMS, Florian BAROUDJIAN, Barouyr DELYON, Julie LALY, Pauline TETU, Pauline LEBBE, Céleste BASSET-SEGUIN, Nicole Sonidegib in the Treatment of Locally Advanced Basal Cell Carcinoma: A Retrospective Study |
title | Sonidegib in the Treatment of Locally Advanced Basal Cell Carcinoma: A Retrospective Study |
title_full | Sonidegib in the Treatment of Locally Advanced Basal Cell Carcinoma: A Retrospective Study |
title_fullStr | Sonidegib in the Treatment of Locally Advanced Basal Cell Carcinoma: A Retrospective Study |
title_full_unstemmed | Sonidegib in the Treatment of Locally Advanced Basal Cell Carcinoma: A Retrospective Study |
title_short | Sonidegib in the Treatment of Locally Advanced Basal Cell Carcinoma: A Retrospective Study |
title_sort | sonidegib in the treatment of locally advanced basal cell carcinoma: a retrospective study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574683/ https://www.ncbi.nlm.nih.gov/pubmed/35604234 http://dx.doi.org/10.2340/actadv.v102.1995 |
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