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Nature medicine · 2026

Neoadjuvant ipilimumab plus nivolumab in melanoma: 5-year survival and biomarker analysis from the phase 2 PRADO-trial.

Клиническое исследование II фазыСтатьяМногоцентровое исследованиеНазвание и аннотация: Перевод в очереди
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Hoeijmakers Lotte L, Dimitriadis Petros, Wijnen Steven C M A, Reijers Irene L M, Lopez-Yurda Marta, Menzies Alexander M, Broeks Annegien, Cornelissen Sten, Torres Acosta Alejandro, van der Wal Anja, Saw Robyn P M, Versluis Judith M, van Houdt Winan J, Wouters Michel W, Romano Jurriaan, Rozeman Eliza A, Grijpink-Ongering Lindsay G, Kapiteijn Ellen, van der Veldt Astrid A M, Suijkerbuijk Karijn P M, Eriksson Hanna, Hospers Geke A P, van der Hage Jos A, Grünhagen Dirk J, Witkamp Arjen J, Lijnsvelt Judith M, Klop Willem M C, Zuur Charlotte L, Bruining Annemarie, Al-Mamgani Abrahim, Pennington Thomas E, Shannon Kerwin F, Ch'ng Sydney, Colebatch Andrew J, Gonzalez Maria, Spillane Andrew J, Haanen John B A G, Rawson Robert V, Scolyer Richard A, van de Wiel Bart A, van Akkooi Alexander C J, Long Georgina V, Blank Christian U

Аннотация

Neoadjuvant ipilimumab plus nivolumab has become standard therapy for stage III melanoma based on the NADINA trial, although long-term data are lacking. In the phase 2 PRADO cohort of OpACIN-neo, 99 patients with stage III macroscopic melanoma received this regimen. Here we report first-time 5-year survival data: 71% event-free survival, 74% relapse-free survival, 79% distant metastasis-free survival and 86% overall survival. Ongoing grade 1-2 immune-related adverse events occurred in 69% of patients alive, predominantly vitiligo and hypothyroidism. Major pathologic response (MPR), high tumor mutational burden (TMB), high interferon-gamma (IFNγ) signature and programmed cell death ligand 1 (PD-L1) expression of 1% or higher were associated with favorable outcomes. Combined high TMB, IFNγ and PD-L1 expression yielded 100% MPR and 100% 5-year event-free survival, whereas triple low expression had only 18% MPR and 41% event-free survival. Our findings demonstrate favorable long-term outcomes for patients with an MPR and identify IFNγ and PD-L1 as promising baseline biomarkers. ClinicalTrials.gov identifier: NCT02977052 .

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты