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)

Author:

Nardin Charlée12ORCID,Hennemann Aymeric1ORCID,Diallo Kadiatou3,Funck-Brentano Elisa4,Puzenat Eve1,Heidelberger Valentine5,Jeudy Géraldine6,Samimi Mahtab7,Lesage Candice8,Boussemart Lise9,Peuvrel Lucie10ORCID,Rouanet Jacques11ORCID,Brunet-Possenti Florence12,Gerard Emilie13,Seris Alice14,Jouary Thomas14ORCID,Saint-Jean Mélanie10ORCID,Puyraveau Marc3,Saiag Philippe4ORCID,Aubin François12

Affiliation:

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

2. Université Franche Comté, Inserm 1098 RIGHT, 25020 Besancon, France

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

4. 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

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

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

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

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

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

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

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

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

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

14. Oncologie Médicale, Centre Hospitalier, 64046 Pau, France

Abstract

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: 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: 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 (n = 44, 52%), nivolumab (n = 35, 41%), ipilimumab (n = 2, 2%), or ipilimumab plus nivolumab (n = 4, 5%). The best overall response rate was 54%. The best response was a complete response in 30 patients (35%), a partial response in 16 patients (19%), stable disease in 18 patients (21%) and progressive disease in 21 patients (25%). Twenty-eight adverse events (AEs) were reported in 23 patients (27%), including 18 grade 1–2 AEs in 14 patients (16%) and 10 grade 3–4 AEs in nine patients (11%). The median progression-free survival (PFS) was 21 months, and the median overall survival (OS) was not reached at the time of analysis. Patients who received another systemic treatment (chemotherapy, targeted therapy or clinical trial) between the two courses of ICI had a lower response to rechallenge (p = 0.035) and shorter PFS (p = 0.016). Conclusion: 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.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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