EClinicalMedicine (Dec 2024)

When to stop immunotherapy for advanced melanoma: the emulated target trialsResearch in context

  • Mathilde Amiot,
  • Laurent Mortier,
  • Stéphane Dalle,
  • Olivier Dereure,
  • Sophie Dalac,
  • Caroline Dutriaux,
  • Marie-Thérèse Leccia,
  • Eve Maubec,
  • Jean-Philippe Arnault,
  • Florence Brunet-Possenti,
  • Julie De Quatrebarbes,
  • Florence Granel-Brocard,
  • Caroline Gaudy-Marqueste,
  • Cecile Pages,
  • Pierre-Emmanuel Stoebner,
  • Philippe Saiag,
  • Thierry Lesimple,
  • Alain Dupuy,
  • Delphine Legoupil,
  • Henri Montaudié,
  • Bastien Oriano,
  • Celeste Lebbe,
  • Raphael Porcher

Journal volume & issue
Vol. 78
p. 102960

Abstract

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Summary: Background: Immune checkpoint inhibitors (ICIs) have demonstrated their efficacy with a 7.5-year overall survival (OS) close to 50% for advanced stages. The design of clinical trials provides for treatment until progression or toxicity, or for a maximum duration of two years. Prolonged follow-up of responders after treatment cessation shows sustained response and a low risk of relapse in the months following cessation. To date, the optimal duration of anti-PD-1 therapy for metastatic melanoma remains unestablished. The objective of this work was to evaluate the optimal duration of ICI administration. Methods: We emulated target trials using the cloning, weighting and censoring approach. Each emulation trial aimed to compare the effect of discontinuing versus continuing ICIs at a specific timepoint, among patients still under treatment and with disease control at that time. Patients were from MelBase between 2015 and 2021. Findings: 435 participants in the MelBase cohort were eligible and were included in the 6-month discontinuation emulated trial. The results showed significantly lower OS when treatment was discontinued, than when treatment was prolonged for at least three months. The 48-month survival difference was 37.8% (95% confidence interval [CI] 19.8–60.5), and the corresponding restricted mean survival time difference was 8.3 months (95% CI: 4.1–12.7). Neither the 12-month nor the 18-month discontinuation emulated trials showed evidence of benefit of either discontinuing or continuing ICIs at either of these timepoints. The 24-month discontinuation emulated trial results were more in favor of discontinuing than continuing treatment at that time point, with an absolute 48-month survival rate that was 10.5% higher (95% CI 4.4–18.1). Interpretation: These results suggest that a one-year course of immunotherapy is both necessary and sufficient for patients with advanced melanoma. Prolonged treatment beyond 2 years does not appear to be beneficial in terms of survival and could even be detrimental. Funding: This work was supported by a grant from Bristol Myers Squibb, Merck Sharp Dhome, Pierre Fabre, Novartis, Sun Pharm, Regeneron, Sanofi, Nektar, Therapeutics and Oncyte.

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