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Bax predicts outcome in gastric cancer patients treated with 5-fluorouracil, leucovorin, and oxaliplatin palliative chemotherapy.
DC Field | Value | Language |
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dc.contributor.author | Jeong, SH | - |
dc.contributor.author | Han, JH | - |
dc.contributor.author | Kim, JH | - |
dc.contributor.author | Ahn, MS | - |
dc.contributor.author | Hwang, YH | - |
dc.contributor.author | Lee, HW | - |
dc.contributor.author | Kang, SY | - |
dc.contributor.author | Park, JS | - |
dc.contributor.author | Choi, JH | - |
dc.contributor.author | Lee, KJ | - |
dc.contributor.author | Sheen, SS | - |
dc.contributor.author | Lim, HY | - |
dc.date.accessioned | 2012-04-23T23:55:15Z | - |
dc.date.available | 2012-04-23T23:55:15Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 0163-2116 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/6508 | - |
dc.description.abstract | BACKGROUND: Platinum and 5-fluorouracil (5-FU)-based regimens have been used the most frequently in palliative chemotherapy for gastric cancer. The present study evaluated the prognostic significance of Bax, excision repair cross-complementation group 1 (ERCC1), and thymidylate synthase (TS) in advanced gastric cancer patients treated with 5-FU, leucovorin, and oxaliplatin (FOLFOX) palliative chemotherapy.
METHODS: Seventy-two patients with metastatic or recurrent gastric cancer were treated with FOLFOX regimen. Pretreatment tumor biopsy specimens were analyzed for Bax, ERCC1, and TS expression by immunohistochemistry. RESULTS: High expression of Bax, ERCC1, and TS was observed in 31 (43%), 33 (46%), and 35 (49%) patients, respectively. The median overall survival (OS) of patients was 12 months. Low expression of Bax was associated with poor OS (median, 9 months vs. 18 months; 2-year, 10% vs. 48%; p=0.0005) in univariate analysis, while expression of ERCC1 and TS was not correlated with patient outcome. In multivariate analysis, low expression of Bax was a significant independent predictor of poor OS (p=0.028). Low expression of Bax was significantly associated with poor survival of patients with metastatic or recurrent gastric cancer treated with FOLFOX chemotherapy. CONCLUSIONS: Immunohistochemical staining for Bax with pretreatment biopsy specimen may be useful in selecting FOLFOX regimen as a treatment option for advanced gastric cancer patients. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Antineoplastic Combined Chemotherapy Protocols | - |
dc.subject.MESH | Biopsy | - |
dc.subject.MESH | DNA-Binding Proteins | - |
dc.subject.MESH | Endonucleases | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Fluorouracil | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Leucovorin | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Organoplatinum Compounds | - |
dc.subject.MESH | Predictive Value of Tests | - |
dc.subject.MESH | Prognosis | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Stomach | - |
dc.subject.MESH | Stomach Neoplasms | - |
dc.subject.MESH | Thymidylate Synthase | - |
dc.subject.MESH | Treatment Outcome | - |
dc.subject.MESH | Tumor Markers, Biological | - |
dc.subject.MESH | bcl-2-Associated X Protein | - |
dc.title | Bax predicts outcome in gastric cancer patients treated with 5-fluorouracil, leucovorin, and oxaliplatin palliative chemotherapy. | - |
dc.type | Article | - |
dc.identifier.pmid | 20503071 | - |
dc.contributor.affiliatedAuthor | 정, 성현 | - |
dc.contributor.affiliatedAuthor | 한, 재호 | - |
dc.contributor.affiliatedAuthor | 김, 장희 | - |
dc.contributor.affiliatedAuthor | 안, 미선 | - |
dc.contributor.affiliatedAuthor | 이, 현우 | - |
dc.contributor.affiliatedAuthor | 강, 석윤 | - |
dc.contributor.affiliatedAuthor | 박, 준성 | - |
dc.contributor.affiliatedAuthor | 최, 진혁 | - |
dc.contributor.affiliatedAuthor | 이, 광재 | - |
dc.contributor.affiliatedAuthor | 신, 승수 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1007/s10620-010-1280-8 | - |
dc.citation.title | Digestive diseases and sciences | - |
dc.citation.volume | 56 | - |
dc.citation.number | 1 | - |
dc.citation.date | 2011 | - |
dc.citation.startPage | 131 | - |
dc.citation.endPage | 138 | - |
dc.identifier.bibliographicCitation | Digestive diseases and sciences, 56(1). : 131-138, 2011 | - |
dc.identifier.eissn | 1573-2568 | - |
dc.relation.journalid | J001632116 | - |
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