Patrick A. Ott,Siwen Hu‐Lieskovan,Bartosz Chmielowski,Ramaswamy Govindan,Aung Naing,Nina Bhardwaj,Kim Margolin,Mark M. Awad,Matthew D. Hellmann,W. Marston Linehan,Terence W. Friedlander,Meghan E. Bushway,Kristen N. Balogh,Tracey Sciuto,Victoria Kohler,Samantha Jane Turnbull,Rana H. Besada,Riley R. Curran,Benjamin Trapp,Julian Scherer
Neoantigens arise from mutations in cancer cells and are important targets of T cell-mediated anti-tumor immunity. Here, we report the first open-label, phase Ib clinical trial of a personalized neoantigen-based vaccine, NEO-PV-01, in combination with PD-1 blockade in patients with advanced melanoma, non-small cell lung cancer, or bladder cancer. This analysis of 82 patients demonstrated that the regimen was safe, with no treatment-related serious adverse events observed. De novo neoantigen-specific CD4+ and CD8+ T cell responses were observed post-vaccination in all of the patients. The vaccine-induced T cells had a cytotoxic phenotype and were capable of trafficking to the tumor and mediating cell killing. In addition, epitope spread to neoantigens not included in the vaccine was detected post-vaccination. These data support the safety and immunogenicity of this regimen in patients with advanced solid tumors (Clinicaltrials.gov: NCT02897765).