Neoadjuvant Nivolumab and Ipilimumab in Resectable Stage III Melanoma.

Détails

ID Serval
serval:BIB_2A38E708B018
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Neoadjuvant Nivolumab and Ipilimumab in Resectable Stage III Melanoma.
Périodique
The New England journal of medicine
Auteur⸱e⸱s
Blank C.U., Lucas M.W., Scolyer R.A., van de Wiel B.A., Menzies A.M., Lopez-Yurda M., Hoeijmakers L.L., Saw RPM, Lijnsvelt J.M., Maher N.G., Pulleman S.M., Gonzalez M., Torres Acosta A., van Houdt W.J., Lo S.N., Kuijpers AMJ, Spillane A., Klop WMC, Pennington T.E., Zuur C.L., Shannon K.F., Seinstra B.A., Rawson R.V., Haanen JBAG, Ch'ng S., Naipal KAT, Stretch J., van Thienen J.V., Rtshiladze M.A., Wilgenhof S., Kapoor R., Meerveld-Eggink A., Grijpink-Ongering L.G., van Akkooi ACJ, Reijers ILM, Gyorki D.E., Grünhagen D.J., Speetjens F.M., Vliek S.B., Placzke J., Spain L., Stassen R.C., Amini-Adle M., Lebbé C., Faries M.B., Robert C., Ascierto P.A., 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 M.C., van den Eertwegh AJM, Boers-Sonderen M.J., Hospers GAP, Carlino M.S., de Groot J.B., Kapiteijn E., Suijkerbuijk KPM, Rutkowski P., Sandhu S., van der Veldt AAM, Long G.V.
ISSN
1533-4406 (Electronic)
ISSN-L
0028-4793
Statut éditorial
In Press
Peer-reviewed
Oui
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: aheadofprint
Résumé
Phase 1-2 trials involving patients with resectable, macroscopic stage III melanoma have shown that neoadjuvant immunotherapy is more efficacious than adjuvant immunotherapy.
In this phase 3 trial, we randomly assigned patients with resectable, macroscopic stage III melanoma, in a 1:1 ratio, to receive two cycles of neoadjuvant ipilimumab plus nivolumab and then undergo surgery or to undergo surgery and then receive 12 cycles of adjuvant nivolumab. Only the patients in the neoadjuvant group who had a partial response or nonresponse received subsequent adjuvant treatment. The primary end point was event-free survival.
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 the 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% among patients in the neoadjuvant group who had a major pathological response, 76.1% among those who had a partial response, and 57.0% among those who had a nonresponse. Adverse events of grade 3 or higher that were related to systemic treatment occurred in 29.7% of the patients in the neoadjuvant group and in 14.7% in the adjuvant group.
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.).
Pubmed
Création de la notice
20/06/2024 14:28
Dernière modification de la notice
21/06/2024 7:08
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