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T-cell Responses to Individualized Neoantigen Therapy mRNA-4157 (V940) Alone or in Combination with Pembrolizumab in the Phase 1 KEYNOTE-603 Study

  • Justin F. Gainor
  • , Manish R. Patel
  • , Jeffrey S. Weber
  • , Martin Gutierrez
  • , Julie E. Bauman
  • , Jeffrey M. Clarke
  • , Ricklie Julian
  • , Aaron J. Scott
  • , Jessica L. Geiger
  • , Kedar Kirtane
  • , Celine Robert-Tissot
  • , Brandon Coder
  • , Moomal Tasneem
  • , Jing Sun
  • , Wei Zheng
  • , Lauren Gerbereux
  • , Andressa Laino
  • , Filippos Porichis
  • , Jack Russella Pollard
  • , Peijie Hou
  • Vasudha Sehgal, Xing Chen, Manju Morrissey, Hikmat N. Daghestani, Igor Feldman, Lakshmi Srinivasan, Joshua P. Frederick, Michelle Brown, Praveen Aanur, Robert Meehan, Howard A. Burris

Research output: Contribution to journalArticlepeer-review

Abstract

mRNA-4157 (V940) is an individualized neoantigen therapy targeting up to 34 patient-specific tumor neoantigens to induce T-cell responses and potentiate antitumor activity. We report mechanistic insights into the immunogenicity of mRNA-4157 via characterization of T-cell responses to neoantigens from the first-in-human, phase 1, KEYNOTE-603 study (NCT03313778) in patients with resected non–small cell lung cancer (Part A: 1-mg mRNA-4157, n = 4) or resected cutaneous melanoma (Part D: 1-mg mRNA-4157 + 200-mg pembrolizumab, n = 12). Safety, tolerability, and immunogenicity were assessed. All patients experienced ≥1 treatment-emergent adverse event; there were no grade 4/5 adverse events or dose-limiting toxicities. mRNA-4157 alone induced consistent de novo and strengthened preexisting T-cell responses to targeted neoantigens. Following combination therapy, sustained mRNA-4157-induced neoantigen-specific T-cell responses and expansion of cytotoxic CD8 and CD4 T cells were observed. These findings show the potential of a novel mRNA individualized neoantigen therapy approach in oncology. Significance: The safety and immunogenicity results from this phase 1 study of mRNA-4157 as adjuvant monotherapy or combination therapy with pembrolizumab show generation of de novo and enhancement of existing neoantigen-specific T-cell responses and provide mechanistic proof of concept to support further development of mRNA-4157 for patients with resected solid tumors.

Original languageEnglish (US)
Pages (from-to)2209-2223
Number of pages15
JournalCancer discovery
Volume14
Issue number11
DOIs
StatePublished - Nov 1 2024
Externally publishedYes

ASJC Scopus subject areas

  • Oncology

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