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The relationship between response to previous systemic treatment and the efficacy of subsequent pemetrexed therapy in advanced non-small cell lung cancer

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dc.contributor.authorSun, Jong-Mu-
dc.contributor.authorOh, Do-Youn-
dc.contributor.authorLee, Se-Hoon-
dc.contributor.authorKim, Dong-Wan-
dc.contributor.authorIm, Seock-Ah-
dc.contributor.authorKim, Tae-You-
dc.contributor.authorLee, Jong Seok-
dc.contributor.authorKim, Young-Whan-
dc.contributor.authorHeo, Dae Seog-
dc.contributor.authorBang, Yung-Jue-
dc.date.accessioned2020-04-27T11:38:20Z-
dc.date.available2020-04-27T11:38:20Z-
dc.date.created2020-02-19-
dc.date.created2020-02-19-
dc.date.issued2010-06-
dc.identifier.citationLung Cancer, Vol.68 No.3, pp.427-432-
dc.identifier.issn0169-5002-
dc.identifier.other91845-
dc.identifier.urihttps://hdl.handle.net/10371/165542-
dc.description.abstractBackground: We sought to identify the relationship between response to previous systemic treatment and the efficacy of subsequent pemetrexed therapy in advanced non-small cell lung cancer (NSCLC). Patients and methods: Two hundred and fifty clinical stage IIIB or IV NSCLC patients treated with pemetrexed as a second-line or further-line treatment between April 2007 and June 2008 were analyzed retrospectively. Prior therapies were divided into four types (gemcitabine-based [G], paclitaxel-based [P] docetaxel-based [D], and EGFR tyrosine kinase inhibitor [I]). Objective response rates (ORR) and progression-free survivals (PFS) for pemetrexed therapy were analyzed according to the response outcome with each previous treatment. Results: The ORR of pemetrexed therapy was higher for patients who had achieved partial response with previous [G] therapy than others (15.0% vs. 4.3%, p = 0.02). In addition, median PFS for pemetrexed therapy was greater for responders to [G] than for nonresponders (3.0 months vs. 1.7 months, p = 0.004). The longer PFS for responders to [G] was also shown in the analysis among patients with squamous cell carcinoma (3.2 months vs. 1.7 months, p = 0.056). By univariate analyses, the variables of the responder to [G] therapy, female, adenocarcinoma, never smoking status, and ECOG performance status of 0-1 were good predictive factors for pemetrexed therapy in terms of PFS. Multivariate analysis revealed that only response to [G] had statistical significance (hazard ratio = 0.62, p = 0.006). Conclusion: Response outcome to prior [G] therapy might predict the efficacy of subsequent pemetrexed therapy in advanced NSCLC. (C) 2009 Elsevier Ireland Ltd. All rights reserved.-
dc.language영어-
dc.publisherElsevier BV-
dc.titleThe relationship between response to previous systemic treatment and the efficacy of subsequent pemetrexed therapy in advanced non-small cell lung cancer-
dc.typeArticle-
dc.contributor.AlternativeAuthor임석아-
dc.identifier.doi10.1016/j.lungcan.2009.07.013-
dc.citation.journaltitleLung Cancer-
dc.identifier.wosid000278478700017-
dc.identifier.scopusid2-s2.0-77952543145-
dc.citation.endpage432-
dc.citation.number3-
dc.citation.startpage427-
dc.citation.volume68-
dc.identifier.sci000278478700017-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorOh, Do-Youn-
dc.contributor.affiliatedAuthorKim, Dong-Wan-
dc.contributor.affiliatedAuthorIm, Seock-Ah-
dc.contributor.affiliatedAuthorKim, Tae-You-
dc.contributor.affiliatedAuthorLee, Jong Seok-
dc.contributor.affiliatedAuthorKim, Young-Whan-
dc.contributor.affiliatedAuthorHeo, Dae Seog-
dc.contributor.affiliatedAuthorBang, Yung-Jue-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusRIBONUCLEOTIDE REDUCTASE-
dc.subject.keywordPlusPHASE-III-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusGEMCITABINE-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusDOCETAXEL-
dc.subject.keywordPlusTRIAL-
dc.subject.keywordPlusTRANSPORTS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorNon-small cell lung cancer-
dc.subject.keywordAuthorChemotherapy-
dc.subject.keywordAuthorPemetrexed-
dc.subject.keywordAuthorGemcitabine-
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  • College of Medicine
  • Department of Medicine
Research Area Clinical Medicine

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