Abstract
In a phase Ib clinical trial, Ott et al. demonstrate feasibility, safety, and immunogenicity of the combination of personalized neoantigen vaccines and PD-1 inhibition in patients with advanced solid tumors. Vaccine-induced T cells persist over time, exhibit cytotoxic potential, and can migrate to tumors. Epitope spread and major pathologic tumor responses were detected following vaccination.
| Original language | English |
|---|---|
| Pages (from-to) | 347-362.e24 |
| Journal | Cell |
| Volume | 183 |
| Issue number | 2 |
| DOIs | |
| State | Published - 15 Oct 2020 |
Keywords
- NEO-PV-01
- T cell
- anti-PD-1
- cancer vaccine
- checkpoint inhibitor
- epitope spread
- immunotherapy
- metastatic cancer
- neoantigen
- personalized vaccine
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