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A phase I/Ib study of OTSGC-A24 combined peptide vaccine in advanced gastric cancer

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dc.contributor.author라선영-
dc.contributor.author김효송-
dc.contributor.author김찬-
dc.date.accessioned2022-08-16T01:29:57Z-
dc.date.available2022-08-16T01:29:57Z-
dc.date.issued2018-03-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/188895-
dc.description.abstractBackground: 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.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherBioMed Central-
dc.relation.isPartOfBMC CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHBiomarkers-
dc.subject.MESHCancer Vaccines / adverse effects-
dc.subject.MESHCancer Vaccines / immunology*-
dc.subject.MESHCancer Vaccines / therapeutic use*-
dc.subject.MESHCombined Modality Therapy-
dc.subject.MESHCytotoxicity, Immunologic-
dc.subject.MESHFemale-
dc.subject.MESHHLA-A24 Antigen / genetics-
dc.subject.MESHHLA-A24 Antigen / immunology-
dc.subject.MESHHaplotypes-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Metastasis-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHStomach Neoplasms / immunology*-
dc.subject.MESHStomach Neoplasms / mortality-
dc.subject.MESHStomach Neoplasms / pathology-
dc.subject.MESHStomach Neoplasms / therapy*-
dc.subject.MESHT-Lymphocytes, Cytotoxic / immunology-
dc.subject.MESHT-Lymphocytes, Cytotoxic / metabolism-
dc.subject.MESHVaccines, Subunit / immunology-
dc.subject.MESHVaccines, Subunit / therapeutic use-
dc.titleA phase I/Ib study of OTSGC-A24 combined peptide vaccine in advanced gastric cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorRaghav Sundar-
dc.contributor.googleauthorSun Young Rha-
dc.contributor.googleauthorHiroki Yamaue-
dc.contributor.googleauthorMasahiro Katsuda-
dc.contributor.googleauthorKoji Kono-
dc.contributor.googleauthorHyo Song Kim-
dc.contributor.googleauthorChan Kim-
dc.contributor.googleauthorKousaku Mimura-
dc.contributor.googleauthorLey-Fang Kua-
dc.contributor.googleauthorWei Peng Yong-
dc.identifier.doi10.1186/s12885-018-4234-8-
dc.contributor.localIdA01316-
dc.contributor.localIdA01202-
dc.contributor.localIdA01034-
dc.relation.journalcodeJ00351-
dc.identifier.eissn1471-2407-
dc.identifier.pmid29587677-
dc.subject.keywordCancer vaccine-
dc.subject.keywordGastric cancer-
dc.subject.keywordOTSGC-A24-
dc.subject.keywordPhase I-
dc.contributor.alternativeNameRha, Sun Young-
dc.contributor.affiliatedAuthor라선영-
dc.contributor.affiliatedAuthor김효송-
dc.contributor.affiliatedAuthor김찬-
dc.citation.volume18-
dc.citation.number1-
dc.citation.startPage332-
dc.identifier.bibliographicCitationBMC CANCER, Vol.18(1) : 332, 2018-03-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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