Authors
Alexander M. M. Eggermont
Christian U. Blank
Mario Mandala
Georgina V. Long
Victoria G. Atkinson
Stéphane Dalle
Andrew M. Haydon
Andrey Meshcheryakov
Adnan Khattak, Edith Cowan UniversityFollow
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
Document Type
Journal Article
Publication Title
Journal of Clinical Oncology
Volume
38
Issue
33
First Page
3925
Last Page
3936
Publisher
ASCO Publications
School
School of Medical and Health Sciences
RAS ID
35334
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 = 514) or placebo (n = 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/Kv 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.
DOI
10.1200/JCO.20.02110
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.
Comments
Eggermont, A. M. M., Blank, C. U., Mandala, M., Long, G. V., Atkinson, V. G., Dalle, S., ... Robert, C. (2020). 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. Journal of Clinical Oncology, 38(33), 3925-3938. https://doi.org/10.1200/JCO.20.02110