Skip to main navigation Skip to search Skip to main content

Longer follow-up confirms recurrence-free survival benefit of adjuvant pembrolizumab in high-risk stage III melanoma: Updated results from the EORTC 1325-MG/KEYNOTE-054 trial

  • Alexander M. M. Eggermont*
  • , Christian U. Blank
  • , Mario Mandala
  • , Georgina V. Long
  • , Victoria G. Atkinson
  • , Stéphane Dalle
  • , Andrew M. Haydon
  • , Andrey Meshcheryakov
  • , Adnan Khattak
  • , Matteo S. Carlino
  • , Shahneen Sandhu
  • , James Larkin
  • , Susana Puig
  • , Paolo A. Ascierto
  • , Piotr Rutkowski
  • , Dirk Schadendorf
  • , Rutger Koornstra
  • , Leonel Hernandez-Aya
  • , Anna Maria di Giacomo
  • , Alfonsus J. M. van den Eertwegh
  • Jean-Jacques Grob, Ralf Gutzmer, Rahima Jamal, Paul C. Lorigan, Alexander C. J. van Akkooi, Clemens Krepler, Nageatte Ibrahim, Sandrine Marreaud, Michal Kicinski, Stefan Suciu, Caroline Robert
*Corresponding author for this work
  • Princess Máxima Center for Pediatric Oncology
  • Netherlands Cancer Institute
  • , Bergamo, Italy
  • The University of Sydney
  • Metro South Integrated Nephrology and Transplant Services (MINTS), Princess Alexandra Hospital, Woolloongabba, Queensland, Australia
  • Department of Stroke Medicine, Lyon, France
  • Alfred Health
  • Russian Academy of Medical Sciences - N.N. Blokhin Russian Cancer Research Center
  • Edith Cowan University
  • Peter Maccallum Cancer Centre
  • Royal Marsden NHS Foundation Trust
  • Hospital Clinic Barcelona
  • IRCCS Istituto nazionale tumori Fondazione Giovanni Pascale - Napoli
  • Maria Sklodowska-Curie Institute of Oncology
  • University of Duisburg-Essen
  • German Cancer Research Center
  • Radboud University Medical Center
  • Washington University St. Louis
  • Azienda Ospedaliera Universitaria Senese
  • Amsterdam UMC - Vrije Universiteit Amsterdam
  • Aix-Marseille Université
  • Hannover Medical School
  • Centre Hospitalier de L'Universite de Montreal
  • The Christie NHS Foundation Trust
  • Merck
  • European Organisation for Research and Treatment of Cancer Data Center
  • Institut Gustave Roussy
  • Princess Máxima Center, Netherlands
  • Princess Alexandra Hospital Brisbane
  • Hospices civils de Lyon
  • Fiona Stanley Hospital and Edith Cowan University, Perth, Australia
  • Royal Marsden Hospital London
  • Hospital Clinic de Barcelona
  • National Center for Tumor Diseases Heidelberg
  • VU Vrije Universiteit
  • Washington University School of Medicine
  • Center for Immuno-Oncology, Siena, Italy
  • Centre Hospitalo-Universitaire Timone
  • University of Montreal
  • Merck & Co, Kenilworth
  • Université Paris-Saclay

Research output: Contribution to journalArticleAcademicpeer-review

30 Downloads (Pure)

Abstract

PURPOSE We conducted the phase III double-blind European Organisation for Research and Treatment of Cancer (EORTC) 1325/KEYNOTE-054 trial to evaluate pembrolizumab versus placebo in patients with resected high-risk stage III melanoma. On the basis of 351 recurrence-free survival (RFS) events at a 1.25-year median follow-up, pembrolizumab prolonged RFS (hazard ratio [HR], 0.57; P,.0001) compared with placebo. This led to the approval of pembrolizumab adjuvant treatment by the European Medicines Agency and US Food and Drug Administration. Here, we report an updated RFS analysis at the 3.05-year median follow-up. PATIENTS AND METHODS A total of 1,019 patients with complete lymph node dissection of American Joint Committee on Cancer Staging Manual (seventh edition; AJCC-7), stage IIIA (at least one lymph node metastasis. 1 mm), IIIB, or IIIC (without in-transit metastasis) cutaneous melanoma were randomly assigned to receive pembrolizumab at a flat dose of 200 mg (n 5 514) or placebo (n 5 505) every 3 weeks for 1 year or until disease recurrence or unacceptable toxicity. The two coprimary end points were RFS in the overall population and in those with programmed death-ligand 1 (PD-L1)-positive tumors. RESULTS Pembrolizumab (190 RFS events) compared with placebo (283 RFS events) resulted in prolonged RFS in the overall population (3-year RFS rate, 63.7% v 44.1% for pembrolizumab v placebo, respectively; HR, 0.56; 95% CI, 0.47 to 0.68) and in the PD-L1-positive tumor subgroup (HR, 0.57; 99% CI, 0.43 to 0.74). The impact of pembrolizumab on RFS was similar in subgroups, in particular according to AJCC-7 and AJCC-8 staging, and BRAF mutation status (HR, 0.51 [99% CI, 0.36 to 0.73] v 0.66 [99% CI, 0.46 to 0.95] for V600E/K v wild type). CONCLUSION In resected high-risk stage III melanoma, pembrolizumab adjuvant therapy provided a sustained and clinically meaningful improvement in RFS at 3-year median follow-up. This improvement was consistent across subgroups.
Original languageEnglish
Pages (from-to)3925-3936
Number of pages12
JournalJournal of clinical oncology
Volume38
Issue number33
DOIs
Publication statusPublished - 20 Nov 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'Longer follow-up confirms recurrence-free survival benefit of adjuvant pembrolizumab in high-risk stage III melanoma: Updated results from the EORTC 1325-MG/KEYNOTE-054 trial'. Together they form a unique fingerprint.

Cite this