Efficacy of Immune Checkpoint Inhibitor (ICI) Rechallenge in Advanced Melanoma Patients' Responders to a First Course of ICI: A Multicenter National Retrospective Study of the French Group of Skin Cancers (Groupe de Cancérologie Cutanée, GCC).

anti-CTLA-4 anti-PD1 disease control immune checkpoint inhibitor immunotherapy melanoma re-induction rechallenge response retreatment safety

Journal

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

Informations de publication

Date de publication:
10 Jul 2023
Historique:
received: 24 04 2023
revised: 07 06 2023
accepted: 29 06 2023
medline: 29 7 2023
pubmed: 29 7 2023
entrez: 29 7 2023
Statut: epublish

Résumé

The long-term effectiveness of immune checkpoint inhibitor (ICI) rechallenge for progressive or recurrent advanced melanoma following previous disease control induced by ICI has not been thoroughly described in the literature. In this retrospective multicenter national real-life study, we enrolled patients who had been rechallenged with an ICI after achieving disease control with a first course of ICI, which was subsequently interrupted. The primary objective was to evaluate tumor response, while the secondary objectives included assessing the safety profile, identifying factors associated with tumor response, and evaluating survival outcomes. A total of 85 patients from 12 centers were included in the study. These patients had advanced (unresectable stage III or stage IV) melanoma that had been previously treated and controlled with a first course of ICI before undergoing rechallenge with ICI. The rechallenge treatments consisted of pembrolizumab ( Rechallenging advanced melanoma patients with ICI after previous disease control induced by these inhibitors resulted in high response rates (54%) and disease control (75%). Therefore, ICI rechallenge should be considered as a relevant therapeutic option.

Sections du résumé

BACKGROUND BACKGROUND
The long-term effectiveness of immune checkpoint inhibitor (ICI) rechallenge for progressive or recurrent advanced melanoma following previous disease control induced by ICI has not been thoroughly described in the literature.
PATIENTS AND METHODS METHODS
In this retrospective multicenter national real-life study, we enrolled patients who had been rechallenged with an ICI after achieving disease control with a first course of ICI, which was subsequently interrupted. The primary objective was to evaluate tumor response, while the secondary objectives included assessing the safety profile, identifying factors associated with tumor response, and evaluating survival outcomes.
RESULTS RESULTS
A total of 85 patients from 12 centers were included in the study. These patients had advanced (unresectable stage III or stage IV) melanoma that had been previously treated and controlled with a first course of ICI before undergoing rechallenge with ICI. The rechallenge treatments consisted of pembrolizumab (
CONCLUSION CONCLUSIONS
Rechallenging advanced melanoma patients with ICI after previous disease control induced by these inhibitors resulted in high response rates (54%) and disease control (75%). Therefore, ICI rechallenge should be considered as a relevant therapeutic option.

Identifiants

pubmed: 37509227
pii: cancers15143564
doi: 10.3390/cancers15143564
pmc: PMC10377277
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Charlée Nardin (C)

Service de Dermatologie, Centre Hospitalier Universitaire, 25000 Besancon, France.
Université Franche Comté, Inserm 1098 RIGHT, 25020 Besancon, France.

Aymeric Hennemann (A)

Service de Dermatologie, Centre Hospitalier Universitaire, 25000 Besancon, France.

Kadiatou Diallo (K)

Centre de Méthodologie Clinique, Centre Hospitalier Universitaire, 25030 Besancon, France.

Elisa Funck-Brentano (E)

Université Paris-Saclay, UVSQ, EA4340-BECCOH, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Ambroise-Paré, Service de Dermatologie Générale et Oncologique, 92104 Boulogne-Billancourt, France.

Eve Puzenat (E)

Service de Dermatologie, Centre Hospitalier Universitaire, 25000 Besancon, France.

Valentine Heidelberger (V)

Service de Dermatologie, Hôpital Robert Ballanger, 93420 Villepinte, France.

Géraldine Jeudy (G)

Service de Dermatologie, Centre Hospitalier Universitaire, Hôpital Le Bocage, 21079 Dijon, France.

Mahtab Samimi (M)

Service de Dermatologie, Centre Hospitalier Universitaire, BIP 1282, INRA-Université de Tours, 37020 Tours, France.

Candice Lesage (C)

Service de Dermatologie, Centre Hospitalier Universitaire, 34295 Montpellier, France.

Lise Boussemart (L)

Service de Dermatologie, Centre Hospitalier Universitaire, Université de Nantes, INSERM, Immunology and New Concepts in Immunotherapy, INCIT, UMR 1302, 44000 Nantes, France.

Lucie Peuvrel (L)

Institut de Cancérologie de l'Ouest, 44800 Saint-Herblain, France.

Jacques Rouanet (J)

Service de Dermatologie, Centre Hospitalier Universitaire, 63003 Clermont-Ferrand, France.

Florence Brunet-Possenti (F)

Service de Dermatologie, Hôpital Bichat AP-HP, Université Paris Cité, 75018 Paris, France.

Emilie Gerard (E)

Service de Dermatologie, Centre Hospitalier Universitaire, 33075 Bordeaux, France.

Alice Seris (A)

Oncologie Médicale, Centre Hospitalier, 64046 Pau, France.

Thomas Jouary (T)

Oncologie Médicale, Centre Hospitalier, 64046 Pau, France.

Mélanie Saint-Jean (M)

Institut de Cancérologie de l'Ouest, 44800 Saint-Herblain, France.

Marc Puyraveau (M)

Centre de Méthodologie Clinique, Centre Hospitalier Universitaire, 25030 Besancon, France.

Philippe Saiag (P)

Université Paris-Saclay, UVSQ, EA4340-BECCOH, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Ambroise-Paré, Service de Dermatologie Générale et Oncologique, 92104 Boulogne-Billancourt, France.

François Aubin (F)

Service de Dermatologie, Centre Hospitalier Universitaire, 25000 Besancon, France.
Université Franche Comté, Inserm 1098 RIGHT, 25020 Besancon, France.

Classifications MeSH