546 A phase I dose escalation study of STEMVAC, a multi-antigen, multi-epitope Th1 selective plasmid-based vaccine, targeting stem cell associated proteins in patients with advanced breast cancer

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oregon; chiles


Background Cancer stem cell or epithelial/mesenchymal transition antigens could have utility in vaccines for cancer treatment and prevention. We identified class II binding T-cell epitopes from non-mutated tumor antigens that selectively elicit a Th1 response. We constructed a 5 antigen (CD105-Yb-1-SOX2-CDH3-MDM2) multi-epitope plasmid-based vaccine; STEMVAC, and conducted a Phase I dose escalation study in patients with advanced breast cancer. Methods Patients with advanced HER2 negative breast cancer previously treated and in remission were sequentially enrolled to 3 dose arms: 150, 300, or 600mcg of STEMVAC. Vaccines were given monthly intradermally for three doses with rhu-GM-CSF (100mcg) as adjuvant. Two booster immunizations (same dose) were given 3 and 6 months after the third vaccine. Primary endpoints were safety and immunogenicity. Secondary endpoints included persistence of the immune response after vaccination and assessment of potential stimulation of T-regulatory (Treg) cells or myeloid derived suppressor cells (MDSC) to the overexpressed non-mutated antigens expressed in STEMVAC. Antigen specific immunity was measured by IFN-gamma (g) and IL-10 ELISPOT. Immune cells were evaluated by flow cytometry. Results Seventy-five percent of patients were hormone receptor positive and 25% triple negative (TNBC). Patient characteristics, including breast cancer subtype, did not vary significantly between doses (all p>0.1). The vast majority of adverse events (AE), 98%, were grades 1/2. The most common AE were injection site reactions, flu-like syndrome, and transient leukopenia and lymphopenia. Arm 1 (150mcg) generated transient low levels of IFN-g secreting T-cells to a median of 1 antigen per patient and considered the least immunogenic dose. Arm 2 (300mcg) resulted in a mean response (sum of all antigens) of 1 antigen specific T-cell per 2500 (1:2500) PBMC at week 16 (p<0.05 compared to baseline) which boosted to 1:1500 by week 60 (p<0.001 compared to baseline). Immune responses for Arm 3 (600mcg) were statistically similar to Arm 2 at 16 weeks, but did not persist and could not be boosted. In Arm 2, booster immunizations increased the incidence and breadth of the immune response, with patients showing significant IFN-g secretion to a median of 4/5 antigens. At 16 weeks, there was no increase in antigen specific IL-10 secreting T-cells, Treg, or MDSC at any dose. Conclusions STEMVAC selectively elicits high level persistent Type I T-cell responses at the 300mcg dose. Two Phase II studies are enrolling; adjuvant setting for TNBC (NCT05455658) and maintenance therapy with pembrolizumab in metastatic non-small cell lung cancer (NCT05242965). Acknowledgements This work was supported by the Department of Defence Breast Cancer Program, VGG, and the Breast Cancer Allliance. We thank all our patient particpants-we could not have completed this study without them. Trial Registration NCT02157051 Ethics Approval The study was approved by the Fred Hutchinson Cancer Research Center Institutional Review Board (#7396). All partcipants gave written informed consent before partcipation in the study.

Clinical Institute


Clinical Institute

Women & Children




Earle A. Chiles Research Institute


Presented at the SITC Annual Meeting; November 8-12; Boston, MA Authors: Mary Disis1, Ying Liu1, Sasha Stanton2, William Gwin1, Andrew Coveler1, John Liao1, Jennifer Childs1 and Denise Cecil1

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