Real-Life Cohort of Patients With Resected High-Risk Melanoma Treated by Adjuvant Anti-PD1 Therapy.

Liza Benzoni, Anaïs Eberhardt, Sarah Milley, Safa Idoudi, Camille Trefcon, Nicolas Romain-Scelle, Luc Thomas, Stéphane Dalle
Author Information
  1. Liza Benzoni: Service de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France. ORCID
  2. Anaïs Eberhardt: Service de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.
  3. Sarah Milley: Service de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.
  4. Safa Idoudi: Service de Dermatologie, Hôpital Saint Louis, Paris, France.
  5. Camille Trefcon: Service de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.
  6. Nicolas Romain-Scelle: Service de Biostatistique, Hospices Civils de Lyon, Hôpital Lyon Sud, Pierre-Bénite, France.
  7. Luc Thomas: Service de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.
  8. Stéphane Dalle: Service de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.

Abstract

BACKGROUND: Programmed cell death protein-1 (PD1) antibodies are currently the standard treatment for resected high-risk melanoma, yet recurrence rate remains high.
OBJECTIVES: This real-life observational study aimed to describe the outcomes of patients with resected high-risk melanoma following adjuvant anti-PD1 immunotherapy and identify factors associated with recurrence risk.
MATERIALS AND METHODS: A total of 235 patients with resected stage III/IV melanoma treated with adjuvant nivolumab or pembrolizumab were included. Imaging scans and cerebral imaging were performed every 12 weeks to detect recurrences. Adverse events were collected. Univariate and multivariate analyses were performed to identify predictive factors of recurrence. Overall survival (OS) and recurrence-free survival (RFS) were estimated.
RESULTS: Among the 235 patients, 103 experienced at least one recurrence (43%); first recurrences were predominantly locoregional (47%). The predictive factor for recurrence identified by multivariate analysis was ulceration (RR 2,03, 95% CI [1,20; 2,86]). RFS was estimated at 75% [70-81] at 12 months and at 64% [58-71] at 24 months. RFS at 12 months was significantly lower in patients with ulcerations (RFS at 83%) compared to those without ulceration (RFS at 66%), p < 0.01. Overall survival (OS) was estimated at 91% [87%-94%] at 12 months and 84% [79%-89%] at 24 months. The OS after a first recurrence was estimated at 69% [60%-80%] at 12 months and decreased to 43% [32%-57%] at 24 months. After a first locoregional recurrence, surgery with a year of adjuvant immunotherapy (40%) was the favoured therapeutic approach. For distant recurrences, clinical trial enrolment was preferred (21%). Double curative immunotherapy was the preferred strategy for cerebral recurrences (30%).
CONCLUSIONS: In this cohort, nearly half of the patients underwent recurrences and RFS at 24 months was 64%. The RFS and OS data were comparable o those reported in the pivotal study Ulceration was the only significant predictive factor for recurrence, associated with decreased RFS at 24 months.

Keywords

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MeSH Term

Humans
Melanoma
Male
Female
Middle Aged
Aged
Neoplasm Recurrence, Local
Chemotherapy, Adjuvant
Antibodies, Monoclonal, Humanized
Immune Checkpoint Inhibitors
Nivolumab
Adult
Programmed Cell Death 1 Receptor
Skin Neoplasms
Aged, 80 and over
Neoplasm Staging

Chemicals

pembrolizumab
Antibodies, Monoclonal, Humanized
Immune Checkpoint Inhibitors
Nivolumab
Programmed Cell Death 1 Receptor
PDCD1 protein, human

Word Cloud

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