A randomized, double-blind, phase III trial of personalized peptide vaccination for recurrent glioblastoma

Neuro Oncol. 2019 Feb 19;21(3):348-359. doi: 10.1093/neuonc/noy200.

Abstract

Background: We conducted a phase III trial of personalized peptide vaccination (PPV) for human leukocyte antigen (HLA)-A24+ recurrent glioblastoma to develop a new treatment modality.

Methods: We randomly assigned 88 recurrent glioblastoma patients to receive PPV (n = 58) or the placebo (n = 30) at a 2-to-1 ratio. Four of 12 warehouse peptides selected based on preexisting peptide-specific immunoglobulin G levels or the corresponding placebos were injected 1×/week for 12 weeks.

Results: Our trial met neither the primary (overall survival [OS]) nor secondary endpoints. Unfavorable factors for OS of 58 PPV patients compared with 30 placebo patients were SART2-93 peptide selection (n = 13 vs 8, hazard ratio [HR]: 15.9), ≥70 years old (4 vs 4, 7.87), >70 kg body weight (10 vs 7, 4.11), and performance status (PS)3 (8 vs 2, 2.82), respectively. Consequently, the median OS for PPV patients without SART2-93 selection plus one of these 3 favorable factors (<70 y old, ≤70 kg, or PS0-2) was significantly longer than that for the corresponding placebo patients (HR: 0.49, 0.44, and 0.51), respectively. Preexisting immunity against both all 12 warehouse peptides besides SART2-93 and the other cytotoxic T lymphocyte epitope peptides was significantly depressed in the patients with SART2-93 selection (n = 21) compared with that of the patients without SART2-93 selection (n = 67). Biomarkers correlative for favorable OS of the PPV patients were a lower percentage of CD11b+CD14+HLA-DRlow immunosuppressive monocytes and a higher percentage of CD4+CD45RA- activated T cells, the intermediate levels of chemokine C-C ligand 2 (CCL2), vascular endothelial growth factor, interleukin (IL)-6, IL-17, or haptoglobin, respectively.

Conclusion: This phase III trial met neither the primary nor secondary endpoints.

Keywords: biomarker for overall survival; personalized peptide vaccine; phase III trial; pre-existing immunity; recurrent glioblastoma.

Publication types

  • Clinical Trial, Phase III
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age Factors
  • Aged
  • Antigens, Neoplasm / immunology*
  • Brain Neoplasms / drug therapy*
  • Brain Neoplasms / immunology
  • Brain Neoplasms / metabolism
  • Cancer Vaccines / therapeutic use*
  • DNA-Binding Proteins / immunology
  • Female
  • Glioblastoma / drug therapy*
  • Glioblastoma / immunology
  • Glioblastoma / metabolism
  • HLA-A24 Antigen / metabolism
  • Humans
  • Karnofsky Performance Status
  • Male
  • Middle Aged
  • Neoplasm Proteins / immunology
  • Neoplasm Recurrence, Local / drug therapy*
  • Neoplasm Recurrence, Local / immunology
  • Neoplasm Recurrence, Local / metabolism
  • Precision Medicine
  • Prognosis
  • Proportional Hazards Models
  • Survival Rate
  • Treatment Outcome
  • Vaccines, Subunit / therapeutic use*
  • Young Adult

Substances

  • Antigens, Neoplasm
  • Cancer Vaccines
  • DNA-Binding Proteins
  • HLA-A24 Antigen
  • Neoplasm Proteins
  • Vaccines, Subunit
  • DSE protein, human