Response to First-Line Treatment with Immune-Checkpoint Inhibitors in Patients with Advanced Cutaneous Squamous Cell Carcinoma: A Multicenter, Retrospective Analysis from the German ADOReg Registry.

advanced cutaneous squamous cell carcinoma cemiplimab checkpoint inhibitor therapy immunosuppression real-world data response durability

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
11 Nov 2022
Historique:
received: 26 10 2022
revised: 08 11 2022
accepted: 09 11 2022
entrez: 26 11 2022
pubmed: 27 11 2022
medline: 27 11 2022
Statut: epublish

Résumé

Cutaneous squamous cell carcinoma (cSCC) is a common malignancy of the skin and has an overall favorable outcome, except for patients with an advanced stage of the disease. The efficacy of checkpoint inhibitors (CPI) for advanced cSCC has been demonstrated in recent clinical studies, but data from real-world cohorts and trial-ineligible cSCC patients are limited. We retrospectively investigated patients with advanced cSCC who have been treated with CPI in a first-line setting at eight German skin cancer centers registered within the multicenter registry ADOReg. Clinical outcome parameters including response, progression-free (PFS) and overall survival (OS), time-to-next-treatment (TTNT), and toxicity were analyzed and have been stratified by the individual immune status. Among 39 evaluable patients, the tumor response rate (rwTRR) was 48.6%, the median PFS was 29.0 months, and the median OS was not reached. In addition, 9 patients showed an impaired immune status due to immunosuppressive medication or hematological diseases. Our data demonstrated that CPI also evoked tumor responses among immunocompromised patients (rwTRR: 48.1 vs. 50.0%), although these responses less often resulted in durable remissions. In line with this, the median PFS (11 vs. 40 months, p = 0.059), TTNT (12 months vs. NR, p = 0.016), and OS (29 months vs. NR, p < 0.001) were significantly shorter for this patient cohort. CPI therapy was well tolerated in both subcohorts with 15% discontinuing therapy due to toxicity. Our real-world data show that first-line CPI therapy produced strong and durable responses among patients with advanced cSCC. Immunocompromised patients were less likely to achieve long-term benefit from anti-PD1 treatment, despite similar tumor response rates.

Identifiants

pubmed: 36428636
pii: cancers14225543
doi: 10.3390/cancers14225543
pmc: PMC9688854
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : Project number: HA 9793/1-1
Organisme : University Medical Center Mainz
ID : Intramural research funding

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Auteurs

Maximilian Haist (M)

Department of Dermatology, University Medical Center Mainz, 55131 Mainz, Germany.
Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Department of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.

Henner Stege (H)

Department of Dermatology, University Medical Center Mainz, 55131 Mainz, Germany.

Berenice Mareen Lang (BM)

Department of Dermatology, University Medical Center Mainz, 55131 Mainz, Germany.

Aikaterini Tsochataridou (A)

Department of Dermatology, University Medical Center Mainz, 55131 Mainz, Germany.

Martin Salzmann (M)

Department of Dermatology and National Center for Tumor Diseases, University Hospital Heidelberg, 69120 Heidelberg, Germany.

Peter Mohr (P)

Department of Dermatology, Elbe Kliniken Buxtehude, 21614 Buxtehude, Germany.

Dirk Schadendorf (D)

Department of Dermatology, University Hospital Essen, 45122 Essen, Germany.

Selma Ugurel (S)

Department of Dermatology, University Hospital Essen, 45122 Essen, Germany.

Jan-Malte Placke (JM)

Department of Dermatology, University Hospital Essen, 45122 Essen, Germany.

Michael Weichenthal (M)

Department of Dermatology, Campus Kiel, University Hospital of Schleswig-Holstein Hospital, 24105 Kiel, Germany.

Ralf Gutzmer (R)

Department of Dermatology and Allergy, Skin Cancer Center Hannover, 30625 Hannover, Germany.

Ulrike Leiter (U)

Center of Dermatooncology, Department of Dermatology, Eberhard-Karls-University, 72076 Tuebingen, Germany.

Martin Kaatz (M)

Department of Dermatology, Wald-Klinikum Gera, 07548 Gera, Germany.

Sebastian Haferkamp (S)

Department of Dermatology, University Hospital Regensburg, 93053 Regensburg, Germany.

Carola Berking (C)

Department of Dermatology, Uniklinikum Erlangen, CCC Erlangen-EMN, Friedrich-Alexander University Erlangen-Nürnberg, 91054 Erlangen, Germany.

Markus Heppt (M)

Department of Dermatology, Uniklinikum Erlangen, CCC Erlangen-EMN, Friedrich-Alexander University Erlangen-Nürnberg, 91054 Erlangen, Germany.

Barbara Tschechne (B)

KRH Klinikum Neustadt am Rübenberge, Specialist for Internal Medicine Hematology and Oncology, 31535 Neustadt, Germany.

Patrick Schummer (P)

Department of Dermatology, University Hospital Würzburg, 97080 Würzburg, Germany.

Christoffer Gebhardt (C)

Skin Cancer Center, Department of Dermatology and Venereology, University Hospital Hamburg-Eppendorf (UKE), 20246 Hamburg, Germany.

Stephan Grabbe (S)

Department of Dermatology, University Medical Center Mainz, 55131 Mainz, Germany.

Carmen Loquai (C)

Department of Dermatology, University Medical Center Mainz, 55131 Mainz, Germany.
Department of Dermatology, Gesundheit-Nord Hospital Bremen, 28102 Bremen, Germany.

Classifications MeSH