Advances in our understanding of T cell activation at a molecular level have permitted the manipulation of T cell regulation in cancer patients. A newly discovered molecule involved in T cell regulation is PD-1, which like CTLA-4 is upregulated on activated CD4 and CD8 T cells but functions through Akt pathways to alter T cell receptor signaling in T cells. A human antibody directed against PD-1 which abrogates its function has been shown in animal tumor models to have potent anti-tumor activity alone and in combination with vaccines. In vitro experiments with melanoma patient peripheral blood mononuclear cell indicated that antibody mediated PD-1 abrogation increased the generation of antigen specific T cells that were lytic, functional, gamma-interferon secreting effector cells. PD-1 antibody increased the proportion of cells that expressed CD107a, augmented avidity and caused an increase in proliferating CD8 cells after antigen exposure, promoting cell survival. PD-1 antibody could also overcome the inhibition of T cell proliferation that occurred in the presence of natural T regulatory cells. When PD-1 blockade was combined with CTLA-4 blockade in vivo in animal models there was an additive or even synergistic anti-tumor effect. When both molecules were abrogated in vitro with human melanoma specific T cells, generation of antigen specific functional T cells was markedly increased. Based on those extensive data, the investigators propose to perform a Phase 1 trial of escalating doses of anti-PD-1 antibody with a multi-peptide vaccine in cohorts of 10 melanoma patients each with endpoints of toxicity, definition of a MTD and comparison of immune and other surrogate assays between cohorts. After a dose of PD-1 antibody given repetitively with a vaccine that optimally stimulates immunity and is well tolerated is defined, the investigators will perform a Phase 2 study of the combination of PD-1 and CTLA-4 abrogating antibodies with a multi-peptide vaccine in patients with chemotherapy resistant metastatic melanoma.

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Programmed Death-1 (PD-1), a molecule found on the surface of activated T cells, delivers inhibitory signals important for the modulation of immunity in animal models. Early testing of an anti-PD-1 antibody using animal tumor models as well as in vitro stimulation of human antigen- specific T cells has shown that PD-1 abrogation results in significant anti-tumor activity and appears to promote the proliferation of high-avidity antigen-specific T cells. In the current proposal, we wish to expand upon those findings to perform clinical trials that assess the toxicity, immune effects and pharmacokinetics of escalating doses of a novel PD-1 abrogating human antibody administered in escalating doses with a multi-peptide vaccine or subsequently at its maximal tolerated dose in a phase II study in combination with an anti-CTLA-4 antibody.

National Institute of Health (NIH)
Food and Drug Administration (FDA)
Research Project (R01)
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Special Emphasis Panel (ZFD1-OPD-N (S1))
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H. Lee Moffitt Cancer Center & Research Institute
United States
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Freeman-Keller, Morganna; Kim, Youngchul; Cronin, Heather et al. (2016) Nivolumab in Resected and Unresectable Metastatic Melanoma: Characteristics of Immune-Related Adverse Events and Association with Outcomes. Clin Cancer Res 22:886-94
Gibney, Geoffrey T; Kudchadkar, Ragini R; DeConti, Ronald C et al. (2015) Safety, correlative markers, and clinical results of adjuvant nivolumab in combination with vaccine in resected high-risk metastatic melanoma. Clin Cancer Res 21:712-20