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Multinational randomized phase III trial with or without consolidation chemotherapy using docetaxel and cisplatin after concurrent chemoradiation in inoperable stage III non-small-cell lung cancer: KCSG-LU05-04

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dc.contributor.authorAhn, Jin Seok-
dc.contributor.authorAhn, Yong Chan-
dc.contributor.authorKim, Joo-Hang-
dc.contributor.authorLee, Chang Geol-
dc.contributor.authorCho, Eun Kyung-
dc.contributor.authorLee, Kyu Chan-
dc.contributor.authorChen, Ming-
dc.contributor.authorKim, Dong-Wan-
dc.contributor.authorKim, Hoon-Kyo-
dc.contributor.authorMin, Young Joo-
dc.contributor.authorKang, Jin-Hyoung-
dc.contributor.authorChoi, Jin-Hyuck-
dc.contributor.authorKim, Sang-We-
dc.contributor.authorZhu, Guangying-
dc.contributor.authorWu, Yi-Long-
dc.contributor.authorKim, Sung Rok-
dc.contributor.authorLee, Kyung Hee-
dc.contributor.authorSong, Hong Suk-
dc.contributor.authorChoi, Yoon-La-
dc.contributor.authorSun, Jong-Mu-
dc.contributor.authorJung, Sin-Ho-
dc.contributor.authorAhn, Myung-Ju-
dc.contributor.authorPark, Keunchil-
dc.date.accessioned2020-04-27T11:20:37Z-
dc.date.available2020-04-27T11:20:37Z-
dc.date.created2018-11-01-
dc.date.issued2015-08-
dc.identifier.citationJournal of Clinical Oncology, Vol.33 No.24, pp.2660-2666-
dc.identifier.issn0732-183X-
dc.identifier.other65076-
dc.identifier.urihttps://hdl.handle.net/10371/165368-
dc.description.abstractPurpose To determine the efficacy of consolidation chemotherapy (CC) with docetaxel and cisplatin (DP) after concurrent chemoradiotherapy (CCRT) with the same agents in locally advanced non-small-cell lung cancer (LA-NSCLC). Patient and Methods Patients were randomly assigned to either CCRT alone (observation arm) or CCRT followed by CC (consolidation arm). CCRT with docetaxel (20 mg/m(2)) and cisplatin (20 mg/m(2)) was administered every week for 6 weeks with a total dose of 66 Gy of thoracic radiotherapy in 33 fractions. In the consolidation arm, patients were further treated with three cycles of DP (35 mg/m(2) each on days 1 and 8, every 3 weeks). The primary end point was 40% improvement in progression-free survival (PFS) compared with observation. Results From October 2005 to April 2011, 437 patients were randomly assigned. Seventeen patients did not start CCRT as a result of consent withdrawal or ineligibility reasons after random assignment, leaving 420 patients for this analysis (n = 211 for observation; n = 209 for consolidation). Patient characteristics were similar in both arms. In the consolidation arm, 143 patients (68%) received CC, of whom 88 (62%) completed three planned cycles. The median PFS was 8.1 months in the observation arm and 9.1 months in the consolidation arm (hazard ratio, 0.91; 95% CI, 0.73 to 1.12; P = .36). Median overall survival times were 20.6 and 21.8 months in the observation and consolidation arms, respectively (HR, 0.91; 95% CI, 0.72 to 1.25; P = .44). Conclusion CC with DP after CCRT with weekly DP in LA-NSCLC failed to further prolong PFS. CCRT alone should remain the standard of care. (C) 2015 by American Society of Clinical Oncology-
dc.language영어-
dc.publisherAmerican Society of Clinical Oncology-
dc.titleMultinational randomized phase III trial with or without consolidation chemotherapy using docetaxel and cisplatin after concurrent chemoradiation in inoperable stage III non-small-cell lung cancer: KCSG-LU05-04-
dc.typeArticle-
dc.contributor.AlternativeAuthor김동완-
dc.identifier.doi10.1200/JCO.2014.60.0130-
dc.citation.journaltitleJournal of Clinical Oncology-
dc.identifier.wosid000361655000015-
dc.identifier.scopusid2-s2.0-84940484434-
dc.citation.endpage2666-
dc.citation.number24-
dc.citation.startpage2660-
dc.citation.volume33-
dc.identifier.sci000361655000015-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorKim, Dong-Wan-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusHYPERFRACTIONATED RADIATION-THERAPY-
dc.subject.keywordPlusBETA-TUBULIN EXPRESSION-
dc.subject.keywordPlusTHORACIC RADIOTHERAPY-
dc.subject.keywordPlus2ND-LINE CHEMOTHERAPY-
dc.subject.keywordPlusDNA-REPAIR-
dc.subject.keywordPlusERCC1-
dc.subject.keywordPlusCHEMORADIOTHERAPY-
dc.subject.keywordPlusCOMBINATION-
dc.subject.keywordPlusETOPOSIDE-
dc.subject.keywordPlusSURVIVAL-
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