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Concurrent chemoradiotherapy followed by adjuvant chemotherapy in uterine cervical cancer patients with high-risk factors

DC Field Value Language
dc.contributor.author성진실-
dc.contributor.author이창걸-
dc.contributor.author조재호-
dc.contributor.author금기창-
dc.contributor.author김귀언-
dc.contributor.author김용배-
dc.contributor.author서창옥-
dc.date.accessioned2014-12-21T16:38:19Z-
dc.date.available2014-12-21T16:38:19Z-
dc.date.issued2007-
dc.identifier.issn0090-8258-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/96066-
dc.description.abstractOBJECTIVES: To determine whether concurrent chemoradiotherapy (CCRT) followed by adjuvant chemotherapy is better than CCRT alone in the management of FIGO stage bulky IB and IIB uterine cervical cancer. METHODS: Two hundred and five FIGO stage bulky IB and IIB patients with squamous cell carcinoma of the uterine cervix treated with CCRT were divided into 2 groups: (1) CCRT alone (n=103, Group A) and (2) CCRT plus adjuvant chemotherapy (n=102, Group B), and treatment outcomes were retrospectively compared between the two patient groups. RESULTS: Only 63% of patients received all three planned cycles of adjuvant chemotherapy, while 16% received only one cycle because of increased treatment-related morbidity or other causes. There were no treatment-related deaths. Although 37 patients experienced failures after completion of treatment, no significant differences were found in patterns of local and regional failures between the two groups. The incidence of distant metastasis, including para-aortic or supraclavicular lymph node metastases, was not reduced in patients of Group B (8% in Group A vs. 7% in Group B). Overall five-year actuarial survival rates for Group A and Group B patients were 85% vs. 80%, and five-year disease-free survival rates were 83% vs. 78%, respectively. CONCLUSIONS: Our data failed to show discernable therapeutic advantage of adjuvant chemotherapy with given after CCRT for the management of FIGO stage bulky IB and IIB uterine cervical cancer patients. A future clinical trial will be necessary to test the clinical efficacy of the adjuvant treatment using newly developed agents in uterine cervical cancer patients.-
dc.description.statementOfResponsibilityopen-
dc.format.extent58~63-
dc.relation.isPartOfGYNECOLOGIC ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols/administration & dosage*-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols/adverse effects-
dc.subject.MESHBrachytherapy-
dc.subject.MESHCarboplatin/administration & dosage-
dc.subject.MESHCarboplatin/adverse effects-
dc.subject.MESHCarcinoma, Squamous Cell/drug therapy*-
dc.subject.MESHCarcinoma, Squamous Cell/pathology-
dc.subject.MESHCarcinoma, Squamous Cell/radiotherapy*-
dc.subject.MESHChemotherapy, Adjuvant/adverse effects-
dc.subject.MESHCisplatin/administration & dosage-
dc.subject.MESHCisplatin/adverse effects-
dc.subject.MESHDose Fractionation, Radiation-
dc.subject.MESHFemale-
dc.subject.MESHFluorouracil/administration & dosage-
dc.subject.MESHFluorouracil/adverse effects-
dc.subject.MESHHumans-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHPrognosis-
dc.subject.MESHRadiotherapy/adverse effects-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHRisk Factors-
dc.subject.MESHUterine Cervical Neoplasms/drug therapy*-
dc.subject.MESHUterine Cervical Neoplasms/pathology-
dc.subject.MESHUterine Cervical Neoplasms/radiotherapy*-
dc.titleConcurrent chemoradiotherapy followed by adjuvant chemotherapy in uterine cervical cancer patients with high-risk factors-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Radiation Oncology (방사선종양학)-
dc.contributor.googleauthorYong Bae Kim-
dc.contributor.googleauthorJae Ho Cho-
dc.contributor.googleauthorGwi Eon Kim-
dc.contributor.googleauthorChang Ok Suh-
dc.contributor.googleauthorJinsil Seong-
dc.contributor.googleauthorChang Geol Lee-
dc.contributor.googleauthorKi Chang Keum-
dc.identifier.doi10.1016/j.ygyno.2006.07.005-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00744-
dc.contributor.localIdA03901-
dc.contributor.localIdA01956-
dc.contributor.localIdA03240-
dc.contributor.localIdA00272-
dc.contributor.localIdA00321-
dc.contributor.localIdA01919-
dc.relation.journalcodeJ00956-
dc.identifier.eissn1095-6859-
dc.identifier.pmid16919718-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0090825806005567-
dc.contributor.alternativeNameSeong, Jin Sil-
dc.contributor.alternativeNameLee, Chang Geol-
dc.contributor.alternativeNameCho, Jae Ho-
dc.contributor.alternativeNameKeum, Ki Chang-
dc.contributor.alternativeNameKim, Gwi Eon-
dc.contributor.alternativeNameKim, Yong Bae-
dc.contributor.alternativeNameSuh, Chang Ok-
dc.contributor.affiliatedAuthorKim, Yong Bae-
dc.contributor.affiliatedAuthorCho, Jae Ho-
dc.contributor.affiliatedAuthorSeong, Jin Sil-
dc.contributor.affiliatedAuthorLee, Chang Geol-
dc.contributor.affiliatedAuthorKeum, Ki Chang-
dc.contributor.affiliatedAuthorKim, Gwi Eon-
dc.contributor.affiliatedAuthorSuh, Chang Ok-
dc.rights.accessRightsnot free-
dc.citation.volume104-
dc.citation.number1-
dc.citation.startPage58-
dc.citation.endPage63-
dc.identifier.bibliographicCitationGYNECOLOGIC ONCOLOGY, Vol.104(1) : 58-63, 2007-
dc.identifier.rimsid35407-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers

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