Frontiers in Immunology (May 2021)

Combining a Universal Telomerase Based Cancer Vaccine With Ipilimumab in Patients With Metastatic Melanoma - Five-Year Follow Up of a Phase I/IIa Trial

  • Elin Aamdal,
  • Elin Aamdal,
  • Elin Aamdal,
  • Else Marit Inderberg,
  • Espen Basmo Ellingsen,
  • Espen Basmo Ellingsen,
  • Espen Basmo Ellingsen,
  • Wenche Rasch,
  • Paal Fredrik Brunsvig,
  • Steinar Aamdal,
  • Steinar Aamdal,
  • Steinar Aamdal,
  • Karen-Marie Heintz,
  • Daniel Vodák,
  • Sigve Nakken,
  • Sigve Nakken,
  • Eivind Hovig,
  • Eivind Hovig,
  • Marta Nyakas,
  • Marta Nyakas,
  • Tormod Kyrre Guren,
  • Gustav Gaudernack,
  • Gustav Gaudernack

DOI
https://doi.org/10.3389/fimmu.2021.663865
Journal volume & issue
Vol. 12

Abstract

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BackgroundIpilimumab improves survival for patients with metastatic malignant melanoma. Combining a therapeutic cancer vaccine with ipilimumab may increase efficacy by providing enhanced anti-tumor immune responses. UV1 consists of three synthetic long peptides from human telomerase reverse transcriptase (hTERT). These peptides comprise epitopes recognized by T cells from cancer patients experiencing long-term survival following treatment with a first-generation hTERT vaccine, and generate long-lasting immune responses in cancer patients when used as monotherapy. The objective of this trial was to investigate the safety and efficacy of combining UV1 with ipilimumab in metastatic melanoma.Patients and MethodsIn this phase I/IIa, single center trial [NCT02275416], patients with metastatic melanoma received repeated UV1 vaccinations, with GM-CSF as an adjuvant, in combination with ipilimumab. Patients were evaluated for safety, efficacy and immune response. Immune responses against vaccine peptides were monitored in peripheral blood by measuring antigen-specific proliferation and IFN-γ production.ResultsTwelve patients were recruited. Adverse events were mainly diarrhea, injection site reaction, pruritus, rash, nausea and fatigue. Ten patients showed a Th1 immune response to UV1 peptides, occurring early and after few vaccinations. Three patients obtained a partial response and one patient a complete response. Overall survival was 50% at 5 years.ConclusionTreatment was well tolerated. The rapid expansion of UV1-specific Th1 cells in the majority of patients indicates synergy between UV1 vaccine and CTLA-4 blockade. This may have translated into clinical benefit, encouraging the combination of UV1 vaccination with standard of care treatment regimes containing ipilimumab/CTLA-4 blocking antibodies.

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