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Vismodegib in Locally Advanced Basal Cell Carcinoma in Slovenia
BACKGROUND: Vismodegib is a first-in-class inhibitor of the hedgehog pathway for treatment of locally advanced basal cell carcinoma (laBCC) and metastatic BCC. OBJECTIVES: The purpose of this study is to report outcomes of patients with laBCC, with basal cell carcinoma nevus syndrome (Gorlin Goltz s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808722/ https://www.ncbi.nlm.nih.gov/pubmed/35896082 http://dx.doi.org/10.1159/000525612 |
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author | Mesti, Tanja Sever, Maša Ocvirk, Janja |
author_facet | Mesti, Tanja Sever, Maša Ocvirk, Janja |
author_sort | Mesti, Tanja |
collection | PubMed |
description | BACKGROUND: Vismodegib is a first-in-class inhibitor of the hedgehog pathway for treatment of locally advanced basal cell carcinoma (laBCC) and metastatic BCC. OBJECTIVES: The purpose of this study is to report outcomes of patients with laBCC, with basal cell carcinoma nevus syndrome (Gorlin Goltz syndrome [G-G Syn]) treated with vismodegib in routine clinical practice in Slovenia in 8.3-year period. METHODS: In this retrospective cohort study, we analyzed baseline characteristics, outcomes, and treatment-related adverse events from locally advanced BCC. The patients were divided into two cohorts: 39 laBCC or multiple BCC patients and 7 patients with G-G Syn who were treated with vismodegib from November 2012 till January 2021. RESULTS: During 100-month period, 46 patients were diagnosed with laBCC (26), multiple BCC (13), and G-G Syn (7), all inappropriate for surgery or radiotherapy. Baseline characteristics: median age was 72.8 years in laBCC + multiple BCC cohort and 47.4 years in G-G Syn cohort. The objective response rate was 80% in laBCC + multiple BCC and 86% in G-G Syn cohort. Disease control rate (DCR) was 95% in laBCC + multiple BCC and 100% in G-G Syn cohort. Median duration of treatment was 9.9 months (range: 1.5–43.1) in laBCC and multiple BCC cohort and 19.5 months (range: 3.6–94.1) in G-G Syn cohort. Majority of treatment-emergent adverse events (TEAEs) in laBCC or multiple BCC cohort were grade 1 or 2 (96%), only 4% of AEs were grade 3. Majority of TEAEs in G-G Syn cohort were also grade 1 or 2 (87%), 13% of AEs were grade 3. No grade 4 or 5 vismodegib-related AEs were reported. CONCLUSION: Vismodegib has shown meaningful efficacy with DCR from 95% to 100% in patients with laBCC, multiple BCC, and G-G Syn in Slovenia. TEAEs were successfully alleviated with multidisciplinary approach and early supportive care. |
format | Online Article Text |
id | pubmed-9808722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-98087222023-01-04 Vismodegib in Locally Advanced Basal Cell Carcinoma in Slovenia Mesti, Tanja Sever, Maša Ocvirk, Janja Dermatology Skin Cancer − Research Article BACKGROUND: Vismodegib is a first-in-class inhibitor of the hedgehog pathway for treatment of locally advanced basal cell carcinoma (laBCC) and metastatic BCC. OBJECTIVES: The purpose of this study is to report outcomes of patients with laBCC, with basal cell carcinoma nevus syndrome (Gorlin Goltz syndrome [G-G Syn]) treated with vismodegib in routine clinical practice in Slovenia in 8.3-year period. METHODS: In this retrospective cohort study, we analyzed baseline characteristics, outcomes, and treatment-related adverse events from locally advanced BCC. The patients were divided into two cohorts: 39 laBCC or multiple BCC patients and 7 patients with G-G Syn who were treated with vismodegib from November 2012 till January 2021. RESULTS: During 100-month period, 46 patients were diagnosed with laBCC (26), multiple BCC (13), and G-G Syn (7), all inappropriate for surgery or radiotherapy. Baseline characteristics: median age was 72.8 years in laBCC + multiple BCC cohort and 47.4 years in G-G Syn cohort. The objective response rate was 80% in laBCC + multiple BCC and 86% in G-G Syn cohort. Disease control rate (DCR) was 95% in laBCC + multiple BCC and 100% in G-G Syn cohort. Median duration of treatment was 9.9 months (range: 1.5–43.1) in laBCC and multiple BCC cohort and 19.5 months (range: 3.6–94.1) in G-G Syn cohort. Majority of treatment-emergent adverse events (TEAEs) in laBCC or multiple BCC cohort were grade 1 or 2 (96%), only 4% of AEs were grade 3. Majority of TEAEs in G-G Syn cohort were also grade 1 or 2 (87%), 13% of AEs were grade 3. No grade 4 or 5 vismodegib-related AEs were reported. CONCLUSION: Vismodegib has shown meaningful efficacy with DCR from 95% to 100% in patients with laBCC, multiple BCC, and G-G Syn in Slovenia. TEAEs were successfully alleviated with multidisciplinary approach and early supportive care. S. Karger AG 2022-07-27 /pmc/articles/PMC9808722/ /pubmed/35896082 http://dx.doi.org/10.1159/000525612 Text en Copyright © 2022 by The Author(s) Published by S. Karger AG, Basel https://creativecommons.org/licenses/by/4.0/This article is licensed under the Creative Commons Attribution 4.0 International License (CC BY). Usage, derivative works and distribution are permitted provided that proper credit is given to the author and the original publisher. |
spellingShingle | Skin Cancer − Research Article Mesti, Tanja Sever, Maša Ocvirk, Janja Vismodegib in Locally Advanced Basal Cell Carcinoma in Slovenia |
title | Vismodegib in Locally Advanced Basal Cell Carcinoma in Slovenia |
title_full | Vismodegib in Locally Advanced Basal Cell Carcinoma in Slovenia |
title_fullStr | Vismodegib in Locally Advanced Basal Cell Carcinoma in Slovenia |
title_full_unstemmed | Vismodegib in Locally Advanced Basal Cell Carcinoma in Slovenia |
title_short | Vismodegib in Locally Advanced Basal Cell Carcinoma in Slovenia |
title_sort | vismodegib in locally advanced basal cell carcinoma in slovenia |
topic | Skin Cancer − Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808722/ https://www.ncbi.nlm.nih.gov/pubmed/35896082 http://dx.doi.org/10.1159/000525612 |
work_keys_str_mv | AT mestitanja vismodegibinlocallyadvancedbasalcellcarcinomainslovenia AT severmasa vismodegibinlocallyadvancedbasalcellcarcinomainslovenia AT ocvirkjanja vismodegibinlocallyadvancedbasalcellcarcinomainslovenia |