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Real-world Treatment Patterns and Outcomes with Systemic Therapies in Unresectable Locally Advanced and Metastatic Cutaneous Squamous Cell Carcinoma in Germany

Advanced cutaneous squamous cell carcinoma is a challenge to treat. Conventional systemic treatment options include chemotherapy and epidermal growth factor receptor-inhibitors. The aim of this study was to assess clinical outcomes with systemic treatments in advanced cutaneous squamous cell carcino...

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Autores principales: KRAMB, Felix, DOERFER, Christoph, MEIWES, Andreas, RAMAKRISHNAN, Karthik, EIGENTLER, Thomas, GARBE, Claus, KEIM, Ulrike, LEITER, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Publication of Acta Dermato-Venereologica 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631247/
https://www.ncbi.nlm.nih.gov/pubmed/34842930
http://dx.doi.org/10.2340/actadv.v101.751
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author KRAMB, Felix
DOERFER, Christoph
MEIWES, Andreas
RAMAKRISHNAN, Karthik
EIGENTLER, Thomas
GARBE, Claus
KEIM, Ulrike
LEITER, Ulrike
author_facet KRAMB, Felix
DOERFER, Christoph
MEIWES, Andreas
RAMAKRISHNAN, Karthik
EIGENTLER, Thomas
GARBE, Claus
KEIM, Ulrike
LEITER, Ulrike
author_sort KRAMB, Felix
collection PubMed
description Advanced cutaneous squamous cell carcinoma is a challenge to treat. Conventional systemic treatment options include chemotherapy and epidermal growth factor receptor-inhibitors. The aim of this study was to assess clinical outcomes with systemic treatments in advanced cutaneous squamous cell carcinoma. Patients receiving systemic treatment at the Tübingen Dermato-Oncology centre between 2007 and 2017 were identified (n = 59). Median age was 76 years (interquartile range (IQR) 71–80 years), 83.1% of patients were male, 72.9% had metastatic cutaneous squamous cell carcinoma, and 27.1% had unresectable locally advanced cutaneous squamous cell carcinoma. During median follow-up of 52 weeks (IQR 27–97 weeks), overall response rate was 14.3%, and disease control rate was 53.6%. Median progression-free survival was 15 weeks (IQR 8–42 weeks), and median overall survival was 52 weeks (IQR 27–97 weeks). Patients receiving chemoradiation vs chemotherapy alone showed better overall survival (hazard ratio 0.41, p = 0.014,) and progression-free survival (hazard ratio 0.42, p = 0.009); no differences were observed for metastatic cutaneous squamous cell carcinoma vs locally advanced cutaneous squamous cell carcinoma patients. Although chemotherapy and/or cetuximab showed limited outcomes in advanced cutaneous squamous cell carcinoma, such therapy may still be an option when anti-PD-1 treatment is contraindicated.
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spelling pubmed-96312472022-11-17 Real-world Treatment Patterns and Outcomes with Systemic Therapies in Unresectable Locally Advanced and Metastatic Cutaneous Squamous Cell Carcinoma in Germany KRAMB, Felix DOERFER, Christoph MEIWES, Andreas RAMAKRISHNAN, Karthik EIGENTLER, Thomas GARBE, Claus KEIM, Ulrike LEITER, Ulrike Acta Derm Venereol Original Article Advanced cutaneous squamous cell carcinoma is a challenge to treat. Conventional systemic treatment options include chemotherapy and epidermal growth factor receptor-inhibitors. The aim of this study was to assess clinical outcomes with systemic treatments in advanced cutaneous squamous cell carcinoma. Patients receiving systemic treatment at the Tübingen Dermato-Oncology centre between 2007 and 2017 were identified (n = 59). Median age was 76 years (interquartile range (IQR) 71–80 years), 83.1% of patients were male, 72.9% had metastatic cutaneous squamous cell carcinoma, and 27.1% had unresectable locally advanced cutaneous squamous cell carcinoma. During median follow-up of 52 weeks (IQR 27–97 weeks), overall response rate was 14.3%, and disease control rate was 53.6%. Median progression-free survival was 15 weeks (IQR 8–42 weeks), and median overall survival was 52 weeks (IQR 27–97 weeks). Patients receiving chemoradiation vs chemotherapy alone showed better overall survival (hazard ratio 0.41, p = 0.014,) and progression-free survival (hazard ratio 0.42, p = 0.009); no differences were observed for metastatic cutaneous squamous cell carcinoma vs locally advanced cutaneous squamous cell carcinoma patients. Although chemotherapy and/or cetuximab showed limited outcomes in advanced cutaneous squamous cell carcinoma, such therapy may still be an option when anti-PD-1 treatment is contraindicated. Society for Publication of Acta Dermato-Venereologica 2022-01-26 /pmc/articles/PMC9631247/ /pubmed/34842930 http://dx.doi.org/10.2340/actadv.v101.751 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
KRAMB, Felix
DOERFER, Christoph
MEIWES, Andreas
RAMAKRISHNAN, Karthik
EIGENTLER, Thomas
GARBE, Claus
KEIM, Ulrike
LEITER, Ulrike
Real-world Treatment Patterns and Outcomes with Systemic Therapies in Unresectable Locally Advanced and Metastatic Cutaneous Squamous Cell Carcinoma in Germany
title Real-world Treatment Patterns and Outcomes with Systemic Therapies in Unresectable Locally Advanced and Metastatic Cutaneous Squamous Cell Carcinoma in Germany
title_full Real-world Treatment Patterns and Outcomes with Systemic Therapies in Unresectable Locally Advanced and Metastatic Cutaneous Squamous Cell Carcinoma in Germany
title_fullStr Real-world Treatment Patterns and Outcomes with Systemic Therapies in Unresectable Locally Advanced and Metastatic Cutaneous Squamous Cell Carcinoma in Germany
title_full_unstemmed Real-world Treatment Patterns and Outcomes with Systemic Therapies in Unresectable Locally Advanced and Metastatic Cutaneous Squamous Cell Carcinoma in Germany
title_short Real-world Treatment Patterns and Outcomes with Systemic Therapies in Unresectable Locally Advanced and Metastatic Cutaneous Squamous Cell Carcinoma in Germany
title_sort real-world treatment patterns and outcomes with systemic therapies in unresectable locally advanced and metastatic cutaneous squamous cell carcinoma in germany
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631247/
https://www.ncbi.nlm.nih.gov/pubmed/34842930
http://dx.doi.org/10.2340/actadv.v101.751
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