Peptide vaccine with glucopyranosyl lipid A–stable oil-in-water emulsion for patients with resected melanoma

Author:

Grewal Eric P1,Erskine Courtney L2,Nevala Wendy K3,Allred Jacob B4,Strand Carrie A4,Kottschade Lisa A1,McWilliams Robert R1,Dronca Roxana S5,Yakovich Adam J6,Markovic Svetomir N1,Block Matthew S1ORCID

Affiliation:

1. Mayo Clinic Rochester, Division of Medical Oncology, 200 First Street SW, Rochester, MN 55905, USA

2. Department of Immunology, 200 First Street SW, Rochester, MN 55905, USA

3. Division of Oncology Research, 200 First Street SW, Rochester, MN 55905, USA

4. Department of Biostatistics & Informatics, 200 First Street SW, Rochester, MN 55905, USA

5. Department of Hematology/Oncology, Mayo Clinic Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA

6. Immune Design, Inc., 1616 Eastlake Ave E #310, Seattle, WA 98102, USA

Abstract

Aim: We tested the safety and immunogenicity of a novel vaccine in patients with resected high-risk melanoma. Patients & methods: HLA-A2-positive patients with resected Stage II–IV melanoma were randomized to receive up to three vaccinations of melanoma-associated peptide (MART-1a) combined with a stable oil-in-water emulsion (SE) either with the Toll-like receptor 4 agonist glucopyranosyl lipid A (GLA-SE–Schedule 1) or alone (SE–Schedule 2). Safety and immunogenicity of the vaccines were monitored. Results: A total of 23 patients were registered. No treatment-related grade 3 or higher adverse events were observed. Increases in MART-1a-specific T cells were seen in 70 and 63% of Schedule 1 and Schedule 2 patients, respectively. Conclusion: Both vaccine schedules were well-tolerated and resulted in an increase in MART-1a-specific T cells. Clinical Trial registration: NCT02320305 ( ClinicalTrials.gov ).

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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