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Efficacy of pemetrexed-based chemotherapy in comparison to non-pemetrexed-based chemotherapy in advanced, ALK plus non-small cell lung cancer

DC Field Value Language
dc.contributor.authorJo, Jaemin-
dc.contributor.authorKim, Se Hyun-
dc.contributor.authorKim, Yu Jung-
dc.contributor.authorLee, Juhyun-
dc.contributor.authorKim, Miso-
dc.contributor.authorKeam, Bhumsuk-
dc.contributor.authorKim, Tae Min-
dc.contributor.authorKim, Dong-Wan-
dc.contributor.authorHeo, Dae Seog-
dc.contributor.authorChung, Jin-Haeng-
dc.contributor.authorJeon, Yoon Kyung-
dc.contributor.authorLee, Jong Seok-
dc.date.accessioned2020-04-27T11:05:44Z-
dc.date.available2020-04-27T11:05:44Z-
dc.date.created2019-04-30-
dc.date.issued2018-03-
dc.identifier.citationYonsei Medical Journal, Vol.59 No.2, pp.202-210-
dc.identifier.issn0513-5796-
dc.identifier.other73419-
dc.identifier.urihttps://hdl.handle.net/10371/165245-
dc.description.abstractPurpose: Previous retrospective studies suggest that anaplastic lymphoma kinase (ALK) mutation-positive (ALK+) non-small cell lung cancer (NSCLC) patients are sensitive to pemetrexed. To determine its efficacy, we retrospectively evaluated clinical outcomes of pemetrexed-based chemotherapy in patients with ALK+ NSCLC. Materials and Methods: We identified 126 patients with advanced, ALK+ NSCLC who received first-line cytotoxic chemotherapy. We compared response, progression-free survival (PFS), and overall survival (OS) rates according to chemotherapy regimens. Furthermore, we evaluated intracranial time to tumor progression (TTP) and proportion of ALK+ cells as prognostic factors. Results: Forty-eight patients received pemetrexed-based chemotherapy, while 78 received other regimens as first-line treatment. The pemetrexed-based chemotherapy group showed superior overall response (44.7% vs. 14.3%, p<0.001) and disease control (85.1% vs. 62.3%, p=0.008) rates. The pemetrexed-based chemotherapy group also exhibited longer PFS (6.6 months vs. 3.8 months, p<0.001); OS rates were not significantly different. The lack of exposure to second-generation ALK inhibitors and intracranial metastasis on initial diagnosis were independent negative prognostic factors of OS. Intracranial TTP was similar between the treatment groups (32.7 months vs. 35.7 months, p=0.733). Patients who harbored a greater number of ALK+ tumor cells (>= 70%) showed prolonged OS on univariate analysis (not reached vs. 44.8 months, p=0.041), but not on multivariate analysis (hazard ratio: 0.19, 95% confidence interval: 0.03-1.42; p=0.106). Conclusion: Pemetrexed-based regimens may prolong PFS in patients with ALK+ NSCLC as a first-line treatment, but are not associated with prolonged OS. Exposure to second-generation ALK inhibitors may improve OS rates in patients with ALK+ NSCLC.-
dc.language영어-
dc.publisher연세대학교의과대학-
dc.titleEfficacy of pemetrexed-based chemotherapy in comparison to non-pemetrexed-based chemotherapy in advanced, ALK plus non-small cell lung cancer-
dc.typeArticle-
dc.contributor.AlternativeAuthor허대석-
dc.contributor.AlternativeAuthor전윤경-
dc.contributor.AlternativeAuthor김동완-
dc.contributor.AlternativeAuthor정진행-
dc.contributor.AlternativeAuthor이종석-
dc.identifier.doi10.3349/ymj.2018.59.2.202-
dc.citation.journaltitleYonsei Medical Journal-
dc.identifier.wosid000425361900006-
dc.identifier.scopusid2-s2.0-85042099444-
dc.citation.endpage210-
dc.citation.number2-
dc.citation.startpage202-
dc.citation.volume59-
dc.identifier.sci000425361900006-
dc.identifier.kciidART002316223-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, Dong-Wan-
dc.contributor.affiliatedAuthorHeo, Dae Seog-
dc.contributor.affiliatedAuthorChung, Jin-Haeng-
dc.contributor.affiliatedAuthorJeon, Yoon Kyung-
dc.contributor.affiliatedAuthorLee, Jong Seok-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusTHYMIDYLATE SYNTHASE-
dc.subject.keywordPlusBRAIN METASTASES-
dc.subject.keywordPlusOPEN-LABEL-
dc.subject.keywordPlusCRIZOTINIB-
dc.subject.keywordPlusTRIAL-
dc.subject.keywordPlusCISPLATIN-
dc.subject.keywordPlusASSOCIATION-
dc.subject.keywordPlusGEMCITABINE-
dc.subject.keywordPlusPERCENTAGE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorAnaplastic lymphoma kinase-
dc.subject.keywordAuthorcarcinoma-
dc.subject.keywordAuthornon-small-cell lung-
dc.subject.keywordAuthorpemetrexed-
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