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A randomized phase 3 trial comparing pemetrexed/carboplatin and docetaxel/carboplatin as first-line treatment for advanced, nonsquamous non-small cell lung cancer

DC Field Value Language
dc.contributor.author김주항-
dc.date.accessioned2014-12-20T17:35:02Z-
dc.date.available2014-12-20T17:35:02Z-
dc.date.issued2011-
dc.identifier.issn1556-0864-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/94875-
dc.description.abstractINTRODUCTION: This study compared survival without toxicity in patients with advanced, nonsquamous non-small cell lung cancer who were treated with first-line pemetrexed/carboplatin or docetaxel/carboplatin. METHODS: This multicenter, open-label, parallel-group, phase 3 trial comprised patients randomized (1:1) to pemetrexed/carboplatin (n = 128) or docetaxel/carboplatin (n = 132). Patients received treatment on day 1 of each 21-day cycle (maximum of six cycles). Treatment included carboplatin (area under the curve = 5 mg/ml × min) and pemetrexed (500 mg/m(2)) or docetaxel (75 mg/m(2)). The primary outcome measure, survival without treatment-emergent grade 3/4 toxicity, was defined as the time from randomization to the first treatment-emergent grade 3/4 adverse event or death and was analyzed using a log-rank test. The analysis population included 106 patients in the pemetrexed/carboplatin (Pem/Carb) group and 105 patients in the docetaxel/carboplatin (Doc/Carb) group. RESULTS: Survival without treatment-emergent grade 3/4 toxicity was significantly longer in the Pem/Carb versus the Doc/Carb group (log-rank p < 0.001; median survival without treatment-emergent grade 3/4 toxicity: 3.2 versus 0.7 months; adjusted hazard ratio = 0.45 [95% confidence interval: 0.34-0.61]). Overall survival was similar in the Pem/Carb versus the Doc/Carb group (log-rank p = 0.934; median survival: 14.9 versus 14.7 months; adjusted hazard ratio = 0.93 [95% confidence interval: 0.66-1.32]). Compared with the Doc/Carb group, fewer patients in the Pem/Carb group experienced grade 3/4 drug-related, treatment-emergent neutropenia, leukopenia, or febrile neutropenia, and more patients experienced anemia and thrombocytopenia. There were three study drug-related deaths during treatment in each group. CONCLUSIONS: The favorable benefit-to-risk profile of pemetrexed/carboplatin suggests that pemetrexed/carboplatin is an appropriate first-line treatment option for chemonaïve patients with advanced, nonsquamous non-small cell lung cancer.-
dc.description.statementOfResponsibilityopen-
dc.format.extent1907~1914-
dc.relation.isPartOfJOURNAL OF THORACIC ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdenocarcinoma/drug therapy*-
dc.subject.MESHAdenocarcinoma/mortality-
dc.subject.MESHAdenocarcinoma/pathology-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols/therapeutic use*-
dc.subject.MESHCarboplatin/administration & dosage-
dc.subject.MESHCarcinoma, Large Cell/drug therapy*-
dc.subject.MESHCarcinoma, Large Cell/mortality-
dc.subject.MESHCarcinoma, Large Cell/pathology-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung/drug therapy*-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung/mortality-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung/pathology-
dc.subject.MESHFemale-
dc.subject.MESHFollow-Up Studies-
dc.subject.MESHGlutamates/administration & dosage-
dc.subject.MESHGuanine/administration & dosage-
dc.subject.MESHGuanine/analogs & derivatives-
dc.subject.MESHHumans-
dc.subject.MESHLung Neoplasms/drug therapy*-
dc.subject.MESHLung Neoplasms/mortality-
dc.subject.MESHLung Neoplasms/pathology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHPemetrexed-
dc.subject.MESHPrognosis-
dc.subject.MESHSurvival Rate-
dc.subject.MESHTaxoids/administration & dosage-
dc.titleA randomized phase 3 trial comparing pemetrexed/carboplatin and docetaxel/carboplatin as first-line treatment for advanced, nonsquamous non-small cell lung cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorRodrigues-Pereira, José-
dc.contributor.googleauthorKim, Joo-Hang-
dc.contributor.googleauthorMagallanes, Manuel-
dc.contributor.googleauthorLee, Dae Ho-
dc.contributor.googleauthorWang, Jie-
dc.contributor.googleauthorGanju, Vinod-
dc.contributor.googleauthorMartínez-Barrera, Luis-
dc.contributor.googleauthorBarraclough, Helen-
dc.contributor.googleauthorvan Kooten, Maximiliano-
dc.contributor.googleauthorOrlando, Mauro-
dc.identifier.doi10.1097/JTO.0b013e318226b5fa-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00945-
dc.relation.journalcodeJ01909-
dc.identifier.eissn1556-1380-
dc.identifier.pmid22005471-
dc.identifier.urlhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&AN=01243894-201111000-00018&LSLINK=80&D=ovft-
dc.subject.keywordCarboplatin-
dc.subject.keywordDocetaxel-
dc.subject.keywordFirst-line therapy-
dc.subject.keywordNon-small cell lung carcinoma-
dc.subject.keywordNonsquamous-
dc.subject.keywordPemetrexed-
dc.contributor.alternativeNameKim, Joo Hang-
dc.contributor.affiliatedAuthorKim, Joo Hang-
dc.rights.accessRightsnot free-
dc.citation.volume6-
dc.citation.number11-
dc.citation.startPage1907-
dc.citation.endPage1914-
dc.identifier.bibliographicCitationJOURNAL OF THORACIC ONCOLOGY, Vol.6(11) : 1907-1914, 2011-
dc.identifier.rimsid27818-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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