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Cumulative incidence rates for CNS and non-CNS progression in two phase II studies of alectinib in ALK-positive NSCLC

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dc.contributor.authorGadgeel, Shirish-
dc.contributor.authorShaw, Alice T.-
dc.contributor.authorBarlesi, Fabrice-
dc.contributor.authorCrino, Lucio-
dc.contributor.authorYang, James Chih-Hsin-
dc.contributor.authorDingemans, Anne-Marie C.-
dc.contributor.authorKim, Dong-Wan-
dc.contributor.authorde Marinis, Filippo-
dc.contributor.authorSchulz, Mathias-
dc.contributor.authorLiu, Shiyao-
dc.contributor.authorGupta, Ravindra-
dc.contributor.authorKotb, Ahmed-
dc.contributor.authorOu, Sai-Hong Ignatius-
dc.date.accessioned2020-04-27T11:05:10Z-
dc.date.available2020-04-27T11:05:10Z-
dc.date.created2019-03-19-
dc.date.issued2018-01-
dc.identifier.citationBritish Journal of Cancer, Vol.118 No.1, pp.38-42-
dc.identifier.issn0007-0920-
dc.identifier.other72783-
dc.identifier.urihttps://hdl.handle.net/10371/165242-
dc.description.abstractBackground: We evaluated the cumulative incidence rate (CIR) of central nervous system (CNS) and non-CNS progression in alectinib-treated patients with anaplastic lymphoma kinase (ALK)-positive non-small-cell lung cancer (NSCLC) to determine the extent to which alectinib may treat or control CNS disease. Methods: Patients with crizotinib-pretreated locally advanced or metastatic disease received alectinib 600 mg orally twice daily in two phase II trials. All patients underwent baseline imaging and regular centrally reviewed scans. Results: At 24 months, the CIR for CNS progression was lower in patients without vs with baseline CNS metastases (8.0 vs 43.9%). Patients with baseline CNS disease and prior radiotherapy had a higher CIR of CNS progression than radiotherapy-naive patients (50.5 vs 27.4%) and a lower CIR of non-CNS progression (25.8 vs 42.5%). Adverse events leading to withdrawal occurred in 5.9% and 6.7% of patients with and without baseline CNS metastases, respectively. Conclusions: This analysis indicates a potential role for alectinib in controlling and preventing CNS metastases.-
dc.language영어-
dc.publisherNature Publishing Group-
dc.titleCumulative incidence rates for CNS and non-CNS progression in two phase II studies of alectinib in ALK-positive NSCLC-
dc.typeArticle-
dc.contributor.AlternativeAuthor김동완-
dc.identifier.doi10.1038/bjc.2017.395-
dc.citation.journaltitleBritish Journal of Cancer-
dc.identifier.wosid000419758900007-
dc.identifier.scopusid2-s2.0-85040316540-
dc.citation.endpage42-
dc.citation.number1-
dc.citation.startpage38-
dc.citation.volume118-
dc.identifier.sci000419758900007-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, Dong-Wan-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusCELL LUNG-CANCER-
dc.subject.keywordPlusOPEN-LABEL-
dc.subject.keywordPlusCRIZOTINIB-
dc.subject.keywordAuthoralectinib-
dc.subject.keywordAuthorALK positive-
dc.subject.keywordAuthorcentral nervous system-
dc.subject.keywordAuthorcumulative incidence rates-
dc.subject.keywordAuthordisease progression-
dc.subject.keywordAuthornon-small-cell lung cancer-
dc.subject.keywordAuthorphase II-
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