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PMID: 23829867 Published · ppublish English Clinical Trial, Phase II Journal Article Research Support, Non-U.S. Gov't

Phase II study of personalized peptide vaccination for refractory bone and soft tissue sarcoma patients.

Cancer science ·Vol. 104 ·No. 10 ·2013-10-00 ·Pages 1285-94

Takahashi R, Ishibashi Y, Hiraoka K, Matsueda S, Kawano K, Kawahara A, Kage M, Ohshima K, Yamanaka R, Shichijo S, Shirouzu K, Itoh K, Sasada T

Abstract

Refractory bone and soft tissue sarcomas are challenging diseases to treat because of their robustness to chemotherapy. Although cancer vaccines have the potential to become an attractive treatment modality, their progress has been hampered by the presence of many subtypes of sarcomas and different human leukocyte antigen (HLA)-types. We investigated whether personalized peptide vaccination (PPV) would be feasible for the vast majority of sarcoma patients. Twenty refractory bone and soft tissue sarcoma patients with nine different subtypes and 11 different HLA-class IA phenotypes were enrolled in this study. A maximum of four HLA-matched peptides showing higher peptide-specific IgG responses in pre-vaccination plasma were selected from 31 pooled peptide candidates applicable for the HLA-A2, -A3, -A11, -A24, -A26, -A31, and -A33 types, and were subcutaneously administered weekly for 6 weeks and bi-weekly thereafter. Measurement of peptide-specific CTL and IgG responses along with other laboratory analyses were conducted before and after vaccination. No patients were excluded by either sarcoma subtypes or different HLA-types. No severe adverse events associated with PPV were observed in any patients. Peptide-specific immunological boosting was observed in the post-vaccination samples from the majority of patients. Tumor reduction of the lung metastasis and a long stable disease was observed in each case, and the median overall survival time of the 20 cases was 9.6 months. Taken together, PPV could be feasible for the vast majority of refractory sarcoma patients because of the safety and higher rates of immunological responses regardless of the presence of different sarcoma subtypes and various HLA-types.

MeSH Terms
Adult Aged Antigens, Neoplasm/analysis Antineoplastic Combined Chemotherapy Protocols/therapeutic use Bone Neoplasms/drug therapy,immunology,therapy Cancer Vaccines/adverse effects,therapeutic use Combined Modality Therapy Cytokines/blood Female Gastrointestinal Diseases/chemically induced HLA Antigens/analysis Hematologic Diseases/chemically induced Humans Immunoglobulin G/blood Immunotherapy, Active/adverse effects Kaplan-Meier Estimate Middle Aged Precision Medicine Salvage Therapy Sarcoma/drug therapy,immunology,therapy Soft Tissue Neoplasms/drug therapy,immunology,therapy T-Lymphocytes, Cytotoxic/immunology Treatment Outcome Vaccination Vaccines, Subunit/adverse effects,therapeutic use Young Adult
Chemicals
Antigens, Neoplasm Cancer Vaccines Cytokines HLA Antigens Immunoglobulin G Vaccines, Subunit
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Takahashi Ryuji
Department of Surgery, Kurume University School of Medicine, Kurume, Japan.
Ishibashi Yukinao
Hiraoka Koji
Matsueda Satoko
Kawano Kouichirou
Kawahara Akihiko
Kage Masayoshi
Ohshima Koichi
Yamanaka Ryuya
Shichijo Shigeki
Shirouzu Kazuo
Itoh Kyogo
Sasada Tetsuro
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Article Info
Journal
Cancer science
Abbr.
Cancer Sci
ISSN
1349-7006
Published
2013-10-00
Epub
2013-00-06
Pages
1285-94
Language
English
Region
England
NLM ID
101168776
PMCID
PMC7656559
Subset
IM
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