作者
Justin F. Gainor,Manish R. Patel,Jeffrey S. Weber,Martin Gutierrez,Julie E. Bauman,Jeffrey Clarke,Ricklie Julian,Aaron J. Scott,J.L. Geiger,Kedar Kirtane,Céline Robert-Tissot,Brandon Coder,Moomal Tasneem,Jing Sun,Wei Zheng,Lauren Gerbereux,Andressa S. Laino,Filippos Porichis,Jack 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
摘要
Abstract mRNA-4157 (V940) is an individualized neoantigen therapy (INT) targeting up to 34 patient-specific tumor neoantigens to induce T cell responses and potentiate anti-tumor 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: 1mg mRNA-4157, n = 4) or resected cutaneous melanoma (Part D: 1mg mRNA-4157 + 200mg pembrolizumab, n = 12). Safety, tolerability, and immunogenicity were assessed. All patients experienced ≥1 treatment-emergent adverse event (AE); there were no grade 4/5 AEs or dose-limiting toxicities. mRNA-4157 alone induced consistent de novo, and strengthened pre-existing, 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 INT approach in oncology.