Combined immune checkpoint blockade for metastatic uveal melanoma: a retrospective, multi-center study.


Journal

Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585

Informations de publication

Date de publication:
13 11 2019
Historique:
received: 20 07 2019
accepted: 30 10 2019
entrez: 15 11 2019
pubmed: 15 11 2019
medline: 3 7 2020
Statut: epublish

Résumé

Uveal melanoma (UM) is highly refractory to treatment with dismal prognosis in advanced stages. The value of the combined checkpoint blockade with CTLA-4 and PD-1 inhibition in metastatic UM is currently unclear. Patients with metastatic or unresectable UM treated with ipilimumab in combination with a PD-1 inhibitor were collected from 16 German skin cancer centers. Patient records of 64 cases were analyzed for response, progression-free survival (PFS), overall survival (OS), and safety. Clinical parameters and serum biomarkers associated with OS and treatment response were determined with Cox regression modelling and logistic regression. The best overall response rate to combined checkpoint blockade was 15.6% with 3.1 and 12.5% complete and partial response, respectively. The median duration of response was 25.5 months (range 9.0-65.0). Stable disease was achieved in 21.9%, resulting in a disease control rate of 37.5% with a median duration of the clinical benefit of 28.0 months (range 7.0-65.0). The median PFS was 3.0 months (95% CI 2.4-3.6). The median OS was estimated to 16.1 months (95% CI 12.9-19.3). Regarding safety, 39.1% of treated patients experienced a severe, treatment-related adverse event according to the CTCAE criteria (grade 3: 37.5%; grade 4: 1.6%). The most common toxicities were colitis (20.3%), hepatitis (20.3%), thyreoiditis (15.6%), and hypophysitis (7.8%). A poor ECOG performance status was an independent risk factor for decreased OS (p = 0.007). The tolerability of the combined checkpoint blockade in UM may possibly be better than in trials on cutaneous melanoma. This study implies that combined checkpoint blockade represents the hitherto most effective treatment option available for metastatic UM available outside of clinical trials.

Sections du résumé

BACKGROUND
Uveal melanoma (UM) is highly refractory to treatment with dismal prognosis in advanced stages. The value of the combined checkpoint blockade with CTLA-4 and PD-1 inhibition in metastatic UM is currently unclear.
METHODS
Patients with metastatic or unresectable UM treated with ipilimumab in combination with a PD-1 inhibitor were collected from 16 German skin cancer centers. Patient records of 64 cases were analyzed for response, progression-free survival (PFS), overall survival (OS), and safety. Clinical parameters and serum biomarkers associated with OS and treatment response were determined with Cox regression modelling and logistic regression.
RESULTS
The best overall response rate to combined checkpoint blockade was 15.6% with 3.1 and 12.5% complete and partial response, respectively. The median duration of response was 25.5 months (range 9.0-65.0). Stable disease was achieved in 21.9%, resulting in a disease control rate of 37.5% with a median duration of the clinical benefit of 28.0 months (range 7.0-65.0). The median PFS was 3.0 months (95% CI 2.4-3.6). The median OS was estimated to 16.1 months (95% CI 12.9-19.3). Regarding safety, 39.1% of treated patients experienced a severe, treatment-related adverse event according to the CTCAE criteria (grade 3: 37.5%; grade 4: 1.6%). The most common toxicities were colitis (20.3%), hepatitis (20.3%), thyreoiditis (15.6%), and hypophysitis (7.8%). A poor ECOG performance status was an independent risk factor for decreased OS (p = 0.007).
CONCLUSIONS
The tolerability of the combined checkpoint blockade in UM may possibly be better than in trials on cutaneous melanoma. This study implies that combined checkpoint blockade represents the hitherto most effective treatment option available for metastatic UM available outside of clinical trials.

Identifiants

pubmed: 31722735
doi: 10.1186/s40425-019-0800-0
pii: 10.1186/s40425-019-0800-0
pmc: PMC6854774
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
CTLA-4 Antigen 0
CTLA4 protein, human 0
Ipilimumab 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

299

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Auteurs

Markus V Heppt (MV)

Department of Dermatology and Allergy, Munich University Hospital (LMU), Frauenlobstr. 9-11, 80337, Munich, Germany.
Department of Dermatology, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Ulmenweg 18, 91054, Erlangen, Germany.

Teresa Amaral (T)

Department of Dermatology, Center for Dermatooncology, University Hospital Tübingen, Liebermeisterstr. 25, 72076, Tübingen, Germany.
Portuguese Air Force Health Care Direction, Lisbon, Portugal.

Katharina C Kähler (KC)

Department of Dermatology, University Hospital Schleswig-Holstein, Campus Kiel, Rosalind-Franklin-Str. 7, 24105, Kiel, Germany.

Lucie Heinzerling (L)

Department of Dermatology, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Ulmenweg 18, 91054, Erlangen, Germany.

Jessica C Hassel (JC)

Skin Cancer Center, Department of Dermatology and National Center for Tumor Diseases (NCT), University Hospital Heidelberg, Im Neuenheimer Feld 460, 69120, Heidelberg, Germany.

Markus Meissner (M)

Department of Dermatology, Venereology and Allergology, Goethe University, Theodor-Stern Kai 7, 60590, Frankfurt am Main, Germany.

Nicole Kreuzberg (N)

Department of Dermatology and Venereology, Skin Cancer Center at the Center of Integrated Oncology (CIO) Köln Bonn, University Hospital of Cologne, Kerpenerstr. 62, 50937, Cologne, Germany.

Carmen Loquai (C)

Department of Dermatology, University Medical Center Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.

Lydia Reinhardt (L)

Department of Dermatology, Skin Cancer Center, Medical Faculty and University Hospital Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307, Dresden, Germany.

Jochen Utikal (J)

Skin Cancer Unit, German Cancer Research Center (DKFZ) and Department of Dermatology, Venereology and Allergology, University Medical Center Mannheim, Ruprecht-Karl University of Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Germany.

Evelyn Dabrowski (E)

Department of Dermatology, Klinikum Ludwigshafen, Bremserstr. 79, 67063, Ludwigshafen, Germany.

Anja Gesierich (A)

Department of Dermatology, University Hospital Würzburg, Josef-Schneider Straße 2, 97080, Würzburg, Germany.

Claudia Pföhler (C)

Department of Dermatology, Saarland University Medical School, Kirrbergerstr, 66421, Homburg/Saar, Germany.

Patrick Terheyden (P)

Department of Dermatology, University of Lübeck, Ratzeburger Allee 160, 23538, Lübeck, Germany.

Kai-Martin Thoms (KM)

Department of Dermatology, University Medical Center Göttingen, Robert-Koch-Str. 40, 37075, Göttingen, Germany.

Lisa Zimmer (L)

Department of Dermatology, University Hospital, University Duisburg-Essen, Hufelandstr. 55, 45147, Essen, Germany.

Thomas K Eigentler (TK)

Department of Dermatology, Center for Dermatooncology, University Hospital Tübingen, Liebermeisterstr. 25, 72076, Tübingen, Germany.

Michael C Kirchberger (MC)

Department of Dermatology, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Ulmenweg 18, 91054, Erlangen, Germany.

Henner M Stege (HM)

Department of Dermatology, University Medical Center Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.

Friedegund Meier (F)

Department of Dermatology, Skin Cancer Center, Medical Faculty and University Hospital Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307, Dresden, Germany.

Max Schlaak (M)

Department of Dermatology and Allergy, Munich University Hospital (LMU), Frauenlobstr. 9-11, 80337, Munich, Germany.

Carola Berking (C)

Department of Dermatology and Allergy, Munich University Hospital (LMU), Frauenlobstr. 9-11, 80337, Munich, Germany. Carola.Berking@uk-erlangen.de.
Department of Dermatology, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Ulmenweg 18, 91054, Erlangen, Germany. Carola.Berking@uk-erlangen.de.

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