PURPOSE Primary analysis of KEYNOTE-942 (ClinicalTrials.gov identifier: NCT03897881 ) demonstrated prolonged recurrence-free survival (RFS) and distant metastasis-free survival (DMFS) for the individualized neoantigen therapy intismeran autogene (intismeran; formerly mRNA-4157 or V940) with pembrolizumab versus pembrolizumab alone in high-risk resected melanoma. This update provides an additional year of follow-up to assess longer-term efficacy/safety. METHODS KEYNOTE-942 is a phase IIb study in patients with completely resected high-risk (stage IIIB to IV) cutaneous melanoma who were randomly assigned to receive either intismeran plus pembrolizumab or pembrolizumab alone. The primary end point was RFS; secondary end points included DMFS and safety/tolerability. Overall survival and biomarker data were exploratory. RESULTS With a median follow-up of approximately 3 years, and a minimum of approximately 2 years (median range 34.9 25.1-51.0 months), the combination continued to demonstrate improvement in RFS (hazard ratio HR, 0.510 80% CI, 0.351 to 0.743) and DMFS (HR, 0.384 80% CI, 0.227 to 0.650) compared with pembrolizumab. The safety profile was consistent with earlier findings. Most adverse events (AEs) were low-grade, with serious AEs, immune-related AEs, and grade 3/4 events comparable between the arms and no grade 4/5 events related to intismeran. CONCLUSION Intismeran plus pembrolizumab significantly prolongs RFS and DMFS compared with pembrolizumab alone for the adjuvant treatment of resected high-risk melanoma.
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Carlino et al. (Sun,) studied this question.
www.synapsesocial.com/papers/699011932ccff479cfe584d9 — DOI: https://doi.org/10.1200/oa-25-00008
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Matteo S. Carlino
Adnan Khattak
Tarek Meniawy
JCO oncology advances.
Harvard University
Massachusetts General Hospital
Washington University in St. Louis
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