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Molecular markers predict distant metastases after adjuvant chemoradiation for rectal cancer.

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dc.contributor.author금기창-
dc.contributor.author금웅섭-
dc.contributor.author김남규-
dc.contributor.author김용배-
dc.contributor.author김준원-
dc.contributor.author김호근-
dc.contributor.author안중배-
dc.contributor.author이익재-
dc.contributor.author조재호-
dc.date.accessioned2014-12-19T16:58:27Z-
dc.date.available2014-12-19T16:58:27Z-
dc.date.issued2012-
dc.identifier.issn0360-3016-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/90542-
dc.description.abstractPURPOSE: The outcomes of adjuvant chemoradiation for locally advanced rectal cancer are nonuniform among patients with matching prognostic factors. We explored the role of molecular markers for predicting the outcome of adjuvant chemoradiation for rectal cancer patients. METHODS AND MATERIALS: The study included 68 patients with stages II to III rectal adenocarcinoma who were treated with total mesorectal excision and adjuvant chemoradiation. Chemotherapy based on 5-fluorouracil and leucovorin was intravenously administered each month for 6-12 cycles. Radiation therapy consisted of 54 Gy delivered in 30 fractions. Immunostaining of surgical specimens for COX-2, EGFR, VEGF, thymidine synthase (TS), and Raf kinase inhibitor protein (RKIP) was performed. RESULTS: The median follow-up was 65 months. Eight locoregional (11.8%) and 13 distant (19.1%) recurrences occurred. Five-year locoregional failure-free survival (LRFFS), distant metastasis-free survival (DMFS), disease-free survival (DFS), and overall survival (OS) rates for all patients were 83.9%, 78.7%, 66.7%, and 73.8%, respectively. LRFFS was not correlated with TNM stage, surgical margin, or any of the molecular markers. VEGF overexpression was significantly correlated with decreased DMFS (P=.045), while RKIP-positive results were correlated with increased DMFS (P=.025). In multivariate analyses, positive findings for COX-2 (COX-2+) and VEGF (VEGF+) and negative findings for RKIP (RKIP-) were independent prognostic factors for DMFS, DFS, and OS (P=.035, .014, and .007 for DMFS; .021, .010, and <.0001 for DFS; and .004, .012, and .001 for OS). The combination of both COX-2+ and VEGF+ (COX-2+/VEGF+) showed a strong correlation with decreased DFS (P=.007), and the combinations of RKIP+/COX-2- and RKIP+/VEGF- showed strong correlations with improved DFS compared with the rest of the patients (P=.001 and <.0001, respectively). CONCLUSIONS: Molecular markers can be valuable in predicting treatment outcome of adjuvant chemoradiation for rectal cancer patients.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdenocarcinoma/chemistry-
dc.subject.MESHAdenocarcinoma/mortality-
dc.subject.MESHAdenocarcinoma/secondary*-
dc.subject.MESHAdenocarcinoma/surgery-
dc.subject.MESHAdenocarcinoma/therapy*-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAntimetabolites, Antineoplastic/therapeutic use-
dc.subject.MESHBiomarkers, Tumor/analysis*-
dc.subject.MESHChemoradiotherapy, Adjuvant*-
dc.subject.MESHCyclooxygenase 2/analysis-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHFemale-
dc.subject.MESHFluorouracil/therapeutic use-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Recurrence, Local/chemistry-
dc.subject.MESHNeoplasm Recurrence, Local/mortality-
dc.subject.MESHPhosphatidylethanolamine Binding Protein/analysis-
dc.subject.MESHRadiation Dosage-
dc.subject.MESHReceptor, Epidermal Growth Factor/analysis-
dc.subject.MESHRectal Neoplasms/chemistry-
dc.subject.MESHRectal Neoplasms/mortality-
dc.subject.MESHRectal Neoplasms/pathology-
dc.subject.MESHRectal Neoplasms/surgery-
dc.subject.MESHRectal Neoplasms/therapy*-
dc.subject.MESHThymidylate Synthase/analysis-
dc.subject.MESHTreatment Outcome-
dc.subject.MESHVascular Endothelial Growth Factor A/analysis-
dc.titleMolecular markers predict distant metastases after adjuvant chemoradiation for rectal cancer.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Radiation Oncology (방사선종양학)-
dc.contributor.googleauthorJun Won Kim-
dc.contributor.googleauthorYong Bae Kim-
dc.contributor.googleauthorJun Jeong Choi-
dc.contributor.googleauthorWoong Sub Koom-
dc.contributor.googleauthorHoguen Kim-
dc.contributor.googleauthorNam-Kyu Kim-
dc.contributor.googleauthorJoong Bae Ahn-
dc.contributor.googleauthorIkjae Lee-
dc.contributor.googleauthorJae Ho Cho-
dc.contributor.googleauthorKi Chang Keum-
dc.identifier.doi22981710-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00272-
dc.contributor.localIdA00273-
dc.contributor.localIdA00353-
dc.contributor.localIdA00958-
dc.contributor.localIdA01183-
dc.contributor.localIdA02262-
dc.contributor.localIdA03055-
dc.contributor.localIdA00744-
dc.contributor.localIdA03901-
dc.relation.journalcodeJ01157-
dc.identifier.eissn1879-355X-
dc.identifier.pmid22981710-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0360301612033160-
dc.subject.keywordAdenocarcinoma/chemistry-
dc.subject.keywordAdenocarcinoma/mortality-
dc.subject.keywordAdenocarcinoma/secondary*-
dc.subject.keywordAdenocarcinoma/surgery-
dc.subject.keywordAdenocarcinoma/therapy*-
dc.subject.keywordAdult-
dc.subject.keywordAged-
dc.subject.keywordAntimetabolites, Antineoplastic/therapeutic use-
dc.subject.keywordBiomarkers, Tumor/analysis*-
dc.subject.keywordChemoradiotherapy, Adjuvant*-
dc.subject.keywordCyclooxygenase 2/analysis-
dc.subject.keywordDisease-Free Survival-
dc.subject.keywordFemale-
dc.subject.keywordFluorouracil/therapeutic use-
dc.subject.keywordHumans-
dc.subject.keywordMale-
dc.subject.keywordMiddle Aged-
dc.subject.keywordNeoplasm Recurrence, Local/chemistry-
dc.subject.keywordNeoplasm Recurrence, Local/mortality-
dc.subject.keywordPhosphatidylethanolamine Binding Protein/analysis-
dc.subject.keywordRadiation Dosage-
dc.subject.keywordReceptor, Epidermal Growth Factor/analysis-
dc.subject.keywordRectal Neoplasms/chemistry-
dc.subject.keywordRectal Neoplasms/mortality-
dc.subject.keywordRectal Neoplasms/pathology-
dc.subject.keywordRectal Neoplasms/surgery-
dc.subject.keywordRectal Neoplasms/therapy*-
dc.subject.keywordThymidylate Synthase/analysis-
dc.subject.keywordTreatment Outcome-
dc.subject.keywordVascular Endothelial Growth Factor A/analysis-
dc.contributor.alternativeNameKeum, Ki Chang-
dc.contributor.alternativeNameKoom, Woong Sub-
dc.contributor.alternativeNameKim, Nam Kyu-
dc.contributor.alternativeNameKim, Yong Bae-
dc.contributor.alternativeNameKim, Jun Won-
dc.contributor.alternativeNameKim, Ho Keun-
dc.contributor.alternativeNameAhn, Joong Bae-
dc.contributor.alternativeNameLee, Ik Jae-
dc.contributor.alternativeNameCho, Jae Ho-
dc.contributor.affiliatedAuthorKeum, Ki Chang-
dc.contributor.affiliatedAuthorKoom, Woong Sub-
dc.contributor.affiliatedAuthorKim, Nam Kyu-
dc.contributor.affiliatedAuthorKim, Jun Won-
dc.contributor.affiliatedAuthorKim, Ho Keun-
dc.contributor.affiliatedAuthorAhn, Joong Bae-
dc.contributor.affiliatedAuthorLee, Ik Jae-
dc.contributor.affiliatedAuthorKim, Yong Bae-
dc.contributor.affiliatedAuthorCho, Jae Ho-
dc.citation.volume84-
dc.citation.number5-
dc.citation.startPage577-
dc.citation.endPage584-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, Vol.84(5) : 577-584, 2012-
dc.identifier.rimsid32823-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers

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