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


Journal

Neuro-oncology
ISSN: 1523-5866
Titre abrégé: Neuro Oncol
Pays: England
ID NLM: 100887420

Informations de publication

Date de publication:
19 02 2019
Historique:
pubmed: 1 12 2018
medline: 6 5 2020
entrez: 1 12 2018
Statut: ppublish

Résumé

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

Sections du résumé

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.

Identifiants

pubmed: 30500939
pii: 5219198
doi: 10.1093/neuonc/noy200
pmc: PMC6380422
doi:

Substances chimiques

Antigens, Neoplasm 0
Cancer Vaccines 0
DNA-Binding Proteins 0
HLA-A24 Antigen 0
Neoplasm Proteins 0
Vaccines, Subunit 0
DSE protein, human EC 5.1.3.19

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

348-359

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Yoshitaka Narita (Y)

National Cancer Center Hospital, Tokyo, Japan.

Yoshiki Arakawa (Y)

Kyoto University Graduate School of Medicine, Kyoto, Japan.

Fumiyuki Yamasaki (F)

Hiroshima University Graduate School of Biomedical and Health Sciences, Hiroshima, Japan.

Ryo Nishikawa (R)

Saitama Medical University International Medical Center, Saitama, Japan.

Tomokazu Aoki (T)

National Hospital Organization, Kyoto Medical Center, Kyoto, Japan.

Masayuki Kanamori (M)

Tohoku University Graduate School of Medicine, Miyagi, Japan.

Motoo Nagane (M)

Kyorin University Faculty of Medicine, Tokyo, Japan.

Toshihiro Kumabe (T)

Kitasato University School of Medicine, Kanagawa, Japan.

Yuichi Hirose (Y)

Fujita Health University School of Medicine, Aichi, Japan.

Tomotsugu Ichikawa (T)

Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Hiroyuki Kobayashi (H)

Hokkaido University Graduate School of Medicine, Hokkaido, Japan.

Takamitsu Fujimaki (T)

Saitama Medical University Hospital, Saitama, Japan.

Hisaharu Goto (H)

Yamaguchi University School of Medicine, Yamaguchi, Japan.

Hideo Takeshima (H)

Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.

Tetsuya Ueba (T)

Kochi Medical School, Kochi, Japan.

Hiroshi Abe (H)

Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

Takashi Tamiya (T)

Kagawa University Faculty of Medicine, Kagawa, Japan.

Yukihiko Sonoda (Y)

Yamagata University Faculty of Medicine, Yamagata, Japan.

Atsushi Natsume (A)

Nagoya University Graduate School of Medicine, Aichi, Japan.

Tatsuyuki Kakuma (T)

Biostatistics Center, Kurume University, Fukuoka, Japan.

Yasuo Sugita (Y)

Kurume University School of Medicine, Fukuoka, Japan.

Nobukazu Komatsu (N)

Kurume University School of Medicine, Fukuoka, Japan.

Akira Yamada (A)

Kurume University School of Medicine, Fukuoka, Japan.

Tetsuro Sasada (T)

Cancer Vaccine Center, Kanagawa Cancer Center Research Institute, Kanagawa, Japan.

Satoko Matsueda (S)

Center for Immunotherapy, Roswell Park Cancer Institute, Buffalo, New York, USA.

Shigeki Shichijo (S)

Cancer Vaccine Center, Kurume University, Fukuoka, Japan.

Kyogo Itoh (K)

Cancer Vaccine Center, Kurume University, Fukuoka, Japan.

Mizuhiko Terasaki (M)

Kurume University School of Medicine, Fukuoka, Japan.

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Classifications MeSH