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5-Fluorouracil, mitomycin-c, and polysaccharide-k versus uracil-ftorafur and polysaccharide-K as adjuvant chemoimmunotherapy for patients with locally advanced gastric cancer with curative resection.
DC Field | Value | Language |
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dc.contributor.author | Ahn, MS | - |
dc.contributor.author | Kang, SY | - |
dc.contributor.author | Lee, HW | - |
dc.contributor.author | Jeong, SH | - |
dc.contributor.author | Park, JS | - |
dc.contributor.author | Lee, KJ | - |
dc.contributor.author | Cho, YK | - |
dc.contributor.author | Han, SU | - |
dc.contributor.author | Lee, SY | - |
dc.contributor.author | Lim, HY | - |
dc.contributor.author | Choi, JH | - |
dc.date.accessioned | 2014-05-21T01:56:31Z | - |
dc.date.available | 2014-05-21T01:56:31Z | - |
dc.date.issued | 2013 | - |
dc.identifier.issn | 0378-584X | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/10051 | - |
dc.description.abstract | BACKGROUND: Despite the small but significant survival benefit of adjuvant chemotherapy in locally advanced gastric cancer (LAGC), the optimal regimen remains to be determined. We conducted a randomized trial comparing oral (PO) chemoimmunotherapy (CITX) with intravenous (IV) CITX in LAGC patients (stages IB-IIIB) with curative resection (≥ D2 dissection).
METHODS: The patients were randomized to the IV (5-fluorouracil 500 mg/m(2) weekly for 24 weeks, mitomycin-C 8 mg/m(2) every 6 weeks × 4) or the PO (uracil-ftorafur (UFT) 400-600 mg/day for 12 months) group. Patients in both groups received PO polysaccharide-K (3 g/day for 4 months). The planned number of patients was 368 for proving the non-inferiority of PO CITX compared to IV CITX for overall survival. RESULTS: The trial was closed prematurely after enrolling 82 patients (44 in the IV group, 38 in the PO group). With a median follow-up of 82 months, there were no significant differences in the 5-year disease-free survival (73% vs. 55%, p = 0.358) and overall survival (77% vs. 66%, p = 0.159) between the 2 groups. The IV group demonstrated a higher incidence of grade 2 or 3 neutropenia, thrombocytopenia, and vomiting. CONCLUSIONS: PO CITX with UFT appeared to be at least non-inferior to 5-fluorouracil and mitomycin-C CITX, with lower toxicity in the adjuvant treatment for LAGC. | - |
dc.format | text/plain | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Antineoplastic Combined Chemotherapy Protocols | - |
dc.subject.MESH | Chemotherapy, Adjuvant | - |
dc.subject.MESH | Disease-Free Survival | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Fluorouracil | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Immunotherapy | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Mitomycin | - |
dc.subject.MESH | Prevalence | - |
dc.subject.MESH | Proteoglycans | - |
dc.subject.MESH | Republic of Korea | - |
dc.subject.MESH | Risk Factors | - |
dc.subject.MESH | Stomach Neoplasms | - |
dc.subject.MESH | Survival Rate | - |
dc.subject.MESH | Tegafur | - |
dc.subject.MESH | Treatment Outcome | - |
dc.subject.MESH | Uracil | - |
dc.title | 5-Fluorouracil, mitomycin-c, and polysaccharide-k versus uracil-ftorafur and polysaccharide-K as adjuvant chemoimmunotherapy for patients with locally advanced gastric cancer with curative resection. | - |
dc.type | Article | - |
dc.identifier.pmid | 23921761 | - |
dc.identifier.url | http://www.karger.com/?DOI=10.1159/000349957 | - |
dc.contributor.affiliatedAuthor | 안, 미선 | - |
dc.contributor.affiliatedAuthor | 강, 석윤 | - |
dc.contributor.affiliatedAuthor | 이, 현우 | - |
dc.contributor.affiliatedAuthor | 정, 성현 | - |
dc.contributor.affiliatedAuthor | 박, 준성 | - |
dc.contributor.affiliatedAuthor | 이, 광재 | - |
dc.contributor.affiliatedAuthor | 조, 용관 | - |
dc.contributor.affiliatedAuthor | 한, 상욱 | - |
dc.contributor.affiliatedAuthor | 이, 순영 | - |
dc.contributor.affiliatedAuthor | 최, 진혁 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1159/000349957 | - |
dc.citation.title | Onkologie | - |
dc.citation.volume | 36 | - |
dc.citation.number | 7-8 | - |
dc.citation.date | 2013 | - |
dc.citation.startPage | 421 | - |
dc.citation.endPage | 426 | - |
dc.identifier.bibliographicCitation | Onkologie, 36(7-8). : 421-426, 2013 | - |
dc.identifier.eissn | 1423-0240 | - |
dc.relation.journalid | J00378584X | - |
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