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Neoadjuvant Nivolumab and Ipilimumab in Resectable Stage III Melanoma.

Authors :
Blank CU
Lucas MW
Scolyer RA
van de Wiel BA
Menzies AM
Lopez-Yurda M
Hoeijmakers LL
Saw RPM
Lijnsvelt JM
Maher NG
Pulleman SM
Gonzalez M
Torres Acosta A
van Houdt WJ
Lo SN
Kuijpers AMJ
Spillane A
Klop WMC
Pennington TE
Zuur CL
Shannon KF
Seinstra BA
Rawson RV
Haanen JBAG
Ch'ng S
Naipal KAT
Stretch J
van Thienen JV
Rtshiladze MA
Wilgenhof S
Kapoor R
Meerveld-Eggink A
Grijpink-Ongering LG
van Akkooi ACJ
Reijers ILM
Gyorki DE
Grünhagen DJ
Speetjens FM
Vliek SB
Placzke J
Spain L
Stassen RC
Amini-Adle M
Lebbé C
Faries MB
Robert C
Ascierto PA
van Rijn R
van den Berkmortel FWPJ
Piersma D
van der Westhuizen A
Vreugdenhil G
Aarts MJB
Stevense-den Boer MAM
Atkinson V
Khattak M
Andrews MC
van den Eertwegh AJM
Boers-Sonderen MJ
Hospers GAP
Carlino MS
de Groot JB
Kapiteijn E
Suijkerbuijk KPM
Rutkowski P
Sandhu S
van der Veldt AAM
Long GV
Source :
The New England journal of medicine [N Engl J Med] 2024 Nov 07; Vol. 391 (18), pp. 1696-1708. Date of Electronic Publication: 2024 Jun 02.
Publication Year :
2024

Abstract

Background: In phase 1-2 trials in patients with resectable, macroscopic stage III melanoma, neoadjuvant immunotherapy was more efficacious than adjuvant immunotherapy.<br />Methods: In this phase 3 trial, we randomly assigned patients with resectable, macroscopic stage III melanoma to two cycles of neoadjuvant ipilimumab plus nivolumab followed by surgery or surgery followed by 12 cycles of adjuvant nivolumab. Only patients in the neoadjuvant group with a partial response or nonresponse received adjuvant treatment. The primary end point was event-free survival.<br />Results: A total of 423 patients underwent randomization. At a median follow-up of 9.9 months, the estimated 12-month event-free survival was 83.7% (99.9% confidence interval [CI], 73.8 to 94.8) in the neoadjuvant group and 57.2% (99.9% CI, 45.1 to 72.7) in the adjuvant group. The difference in restricted mean survival time was 8.00 months (99.9% CI, 4.94 to 11.05; P<0.001; hazard ratio for progression, recurrence, or death, 0.32; 99.9% CI, 0.15 to 0.66). In the neoadjuvant group, 59.0% of patients had a major pathological response, 8.0% had a partial response, 26.4% had a nonresponse (>50% residual viable tumor), and 2.4% had progression; in 4.2%, surgery had not yet been performed or was omitted. The estimated 12-month recurrence-free survival was 95.1% in patients in the neoadjuvant group who had a major pathological response, 76.1% among those with a partial response, and 57.0% among those with a nonresponse. Adverse events of grade 3 or higher that were related to systemic treatment occurred in 29.7% of patients in the neoadjuvant group and in 14.7% in the adjuvant group.<br />Conclusions: Among patients with resectable, macroscopic stage III melanoma, neoadjuvant ipilimumab plus nivolumab followed by surgery and response-driven adjuvant therapy resulted in longer event-free survival than surgery followed by adjuvant nivolumab. (Funded by Bristol Myers Squibb and others; NADINA ClinicalTrials.gov number, NCT04949113.).<br /> (Copyright © 2024 Massachusetts Medical Society.)

Details

Language :
English
ISSN :
1533-4406
Volume :
391
Issue :
18
Database :
MEDLINE
Journal :
The New England journal of medicine
Publication Type :
Academic Journal
Accession number :
38828984
Full Text :
https://doi.org/10.1056/NEJMoa2402604