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Concurrent chemoradiotherapy with doxifluridine and paclitaxel for extrahepatic bile duct cancer

DC Field Value Language
dc.contributor.author김경식-
dc.contributor.author박승우-
dc.contributor.author박정엽-
dc.contributor.author성진실-
dc.contributor.author송시영-
dc.contributor.author이우정-
dc.contributor.author정재복-
dc.date.accessioned2015-06-10T12:58:03Z-
dc.date.available2015-06-10T12:58:03Z-
dc.date.issued2006-
dc.identifier.issn0277-3732-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/110770-
dc.description.abstractOBJECTIVES: Bile duct cancer is a rare malignancy with poor prognosis. We sought to determine the efficacy of concurrent chemoradiotherapy with doxifluridine and paclitaxel for extrahepatic bile duct cancer. METHODS: Nineteen patients with unresectable extrahepatic bile duct cancer received doxifluridine (600 mg/m2) daily, intravenous paclitaxel (50 mg/m) weekly (before radiotherapy), and radiotherapy of 4500 cGy for approximately 5 weeks. RESULTS: Local response rate which reflected the reopening of occluded bile duct was 89.5% (17 out of 19). In 6 cases (31.6%), overall response, which measured the change of tumor size, was achieved with this treatment. The longest survival time was 52 months, and median survival time was 14 months. One- and 2-year survival rates were 84.2% and 31.6%, respectively. One case of gastrointestinal bleeding and 1 case of grade III leukopenia occurred during the treatment. One patient could not finish the treatment because of poor general condition. CONCLUSIONS: Concurrent chemoradiotherapy with doxifluridine and paclitaxel seemed to produce a good clinical response without severe toxicity and improve survival rates in patients with extrahepatic bile duct cancer.-
dc.description.statementOfResponsibilityopen-
dc.format.extent240~245-
dc.relation.isPartOfAMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdministration, Oral-
dc.subject.MESHAged-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols/adverse effects-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols/therapeutic use*-
dc.subject.MESHBile Duct Neoplasms/drug therapy*-
dc.subject.MESHBile Duct Neoplasms/radiotherapy*-
dc.subject.MESHBile Ducts, Extrahepatic*-
dc.subject.MESHCombined Modality Therapy-
dc.subject.MESHFemale-
dc.subject.MESHFloxuridine/administration & dosage-
dc.subject.MESHHumans-
dc.subject.MESHInfusions, Intravenous-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPaclitaxel/administration & dosage-
dc.subject.MESHSurvival Analysis-
dc.subject.MESHTreatment Outcome-
dc.titleConcurrent chemoradiotherapy with doxifluridine and paclitaxel for extrahepatic bile duct cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Surgery (외과학)-
dc.contributor.googleauthorJeong Youp Park-
dc.contributor.googleauthorSeung Woo Park-
dc.contributor.googleauthorJae Bock Chung-
dc.contributor.googleauthorJinsil Seong-
dc.contributor.googleauthorKyung Sik Kim-
dc.contributor.googleauthorWoo Jung Lee-
dc.contributor.googleauthorSi Young Song-
dc.identifier.doi10.1097/01.coc.0000217829.77404.22-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00299-
dc.contributor.localIdA01551-
dc.contributor.localIdA01647-
dc.contributor.localIdA01956-
dc.contributor.localIdA02035-
dc.contributor.localIdA03706-
dc.contributor.localIdA02993-
dc.relation.journalcodeJ00075-
dc.identifier.eissn1537-453X-
dc.identifier.pmid16755176-
dc.identifier.urlhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&AN=00000421-200606000-00005&LSLINK=80&D=ovft-
dc.subject.keywordchemoradiotherapy-
dc.subject.keyworddoxifluridine-
dc.subject.keywordpaclitaxel-
dc.subject.keywordextrahepatic bile duct cancer-
dc.contributor.alternativeNameKim, Kyung Sik-
dc.contributor.alternativeNamePark, Seung Woo-
dc.contributor.alternativeNamePark, Jeong Youp-
dc.contributor.alternativeNameSeong, Jin Sil-
dc.contributor.alternativeNameSong, Si Young-
dc.contributor.alternativeNameLee, Woo Jung-
dc.contributor.alternativeNameChung, Jae Bock-
dc.contributor.affiliatedAuthorKim, Kyung Sik-
dc.contributor.affiliatedAuthorPark, Seung Woo-
dc.contributor.affiliatedAuthorPark, Jeong Youp-
dc.contributor.affiliatedAuthorSeong, Jin Sil-
dc.contributor.affiliatedAuthorSong, Si Young-
dc.contributor.affiliatedAuthorChung, Jae Bock-
dc.contributor.affiliatedAuthorLee, Woo Jung-
dc.rights.accessRightsnot free-
dc.citation.volume29-
dc.citation.number3-
dc.citation.startPage240-
dc.citation.endPage245-
dc.identifier.bibliographicCitationAMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, Vol.29(3) : 240-245, 2006-
dc.identifier.rimsid54421-
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 Radiation Oncology (방사선종양학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers

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