Cited 32 times in
A phase I/Ib study of OTSGC-A24 combined peptide vaccine in advanced gastric cancer
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 라선영 | - |
dc.contributor.author | 김효송 | - |
dc.contributor.author | 김찬 | - |
dc.date.accessioned | 2022-08-16T01:29:57Z | - |
dc.date.available | 2022-08-16T01:29:57Z | - |
dc.date.issued | 2018-03 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/188895 | - |
dc.description.abstract | Background: We conducted a phase I/Ib, open-label, single-arm trial to assess the safety, tolerability and optimal scheduling regimen of OTSGC-A24 cancer vaccine in patients with advanced gastric cancer. Methods: Patients with advanced gastric cancer with HLA-A*24:02 haplotype were included in this study. OTSGC-A24 was administered at 1 mg in 3-weekly (3w), 2-weekly (2w), and weekly (1w) cohorts to evaluate the safety, immunological response and schedule. Based on the highest specific cytotoxic T lymphocyte (CTL) induction rate at 4 weeks, using the ELISPOT test, cohorts were expanded to define the optimal dosing schedule for OTSGC-A24. Results: In this study, 24 advanced gastric cancer patients with HLA-A*24:02 haplotype were enrolled and treated in 3 cohorts (3w cohort: 3; 2w cohort: 11 and 1w cohort: 10 patients). The most common adverse events were decreased appetite (29%), diarrhea (21%), myalgia (25%). The most common treatment-related adverse event was injection site erythema (25%). No dose-limiting toxicities were observed in any cohort and OTSGC-A24 was well tolerated. Positive CTL responses after vaccination were observed in 15 patients (75%) at 4 weeks: 3w cohort (33%), 2w cohort (88%), 1w cohort (78%). At 12 weeks, 18 patients had responded (90%); 3w cohort (100%), 2w cohort (100%), 1w cohort (78%). The best radiological was stable disease (40%). Median progression free survival was 1.7 months (95% CI: 1.4 to 3.5) and median overall survival was 5.7 months (95% CI 3.8 to 8.6). Conclusions: OTSGC-A24 combined peptide cancer vaccine was well tolerated. Significant responses in CTL were observed and the recommended phase 2 dose is 1 mg OTSGC-A24 sub-cutaneous, every 2 weeks. Although no radiological response was observed, a respectable overall survival was achieved, consistent with other immunotherapy agents being investigated in gastric cancer. Trial registration: ClinicalTrials.gov Identifier: NCT01227772 , Date registered: 21 Oct 2010. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | BioMed Central | - |
dc.relation.isPartOf | BMC CANCER | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Biomarkers | - |
dc.subject.MESH | Cancer Vaccines / adverse effects | - |
dc.subject.MESH | Cancer Vaccines / immunology* | - |
dc.subject.MESH | Cancer Vaccines / therapeutic use* | - |
dc.subject.MESH | Combined Modality Therapy | - |
dc.subject.MESH | Cytotoxicity, Immunologic | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | HLA-A24 Antigen / genetics | - |
dc.subject.MESH | HLA-A24 Antigen / immunology | - |
dc.subject.MESH | Haplotypes | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Neoplasm Metastasis | - |
dc.subject.MESH | Neoplasm Staging | - |
dc.subject.MESH | Stomach Neoplasms / immunology* | - |
dc.subject.MESH | Stomach Neoplasms / mortality | - |
dc.subject.MESH | Stomach Neoplasms / pathology | - |
dc.subject.MESH | Stomach Neoplasms / therapy* | - |
dc.subject.MESH | T-Lymphocytes, Cytotoxic / immunology | - |
dc.subject.MESH | T-Lymphocytes, Cytotoxic / metabolism | - |
dc.subject.MESH | Vaccines, Subunit / immunology | - |
dc.subject.MESH | Vaccines, Subunit / therapeutic use | - |
dc.title | A phase I/Ib study of OTSGC-A24 combined peptide vaccine in advanced gastric cancer | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.googleauthor | Raghav Sundar | - |
dc.contributor.googleauthor | Sun Young Rha | - |
dc.contributor.googleauthor | Hiroki Yamaue | - |
dc.contributor.googleauthor | Masahiro Katsuda | - |
dc.contributor.googleauthor | Koji Kono | - |
dc.contributor.googleauthor | Hyo Song Kim | - |
dc.contributor.googleauthor | Chan Kim | - |
dc.contributor.googleauthor | Kousaku Mimura | - |
dc.contributor.googleauthor | Ley-Fang Kua | - |
dc.contributor.googleauthor | Wei Peng Yong | - |
dc.identifier.doi | 10.1186/s12885-018-4234-8 | - |
dc.contributor.localId | A01316 | - |
dc.contributor.localId | A01202 | - |
dc.contributor.localId | A01034 | - |
dc.relation.journalcode | J00351 | - |
dc.identifier.eissn | 1471-2407 | - |
dc.identifier.pmid | 29587677 | - |
dc.subject.keyword | Cancer vaccine | - |
dc.subject.keyword | Gastric cancer | - |
dc.subject.keyword | OTSGC-A24 | - |
dc.subject.keyword | Phase I | - |
dc.contributor.alternativeName | Rha, Sun Young | - |
dc.contributor.affiliatedAuthor | 라선영 | - |
dc.contributor.affiliatedAuthor | 김효송 | - |
dc.contributor.affiliatedAuthor | 김찬 | - |
dc.citation.volume | 18 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 332 | - |
dc.identifier.bibliographicCitation | BMC CANCER, Vol.18(1) : 332, 2018-03 | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.