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Olmutinib in T790M-positive non-small cell lung cancer after failure of first-line epidermal growth factor receptor-tyrosine kinase inhibitor therapy: A global, phase 2 study

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dc.contributor.authorPark, Keunchil-
dc.contributor.authorJanne, Pasi A.-
dc.contributor.authorKim, Dong-Wan-
dc.contributor.authorHan, Ji-Youn-
dc.contributor.authorWu, Ming-Fang-
dc.contributor.authorLee, Jong-Seok-
dc.contributor.authorKang, Jin-Hyoung-
dc.contributor.authorLee, Dae Ho-
dc.contributor.authorCho, Byoung Chul-
dc.contributor.authorYu, Chong-Jen-
dc.contributor.authorPang, Yong Kek-
dc.contributor.authorFelip, Enriqueta-
dc.contributor.authorKim, Hyunjin-
dc.contributor.authorBaek, Eunhye-
dc.contributor.authorNoh, Young Su-
dc.date.accessioned2023-03-20T08:54:27Z-
dc.date.available2023-03-20T08:54:27Z-
dc.date.created2021-07-06-
dc.date.created2021-07-06-
dc.date.issued2021-05-
dc.identifier.citationCancer, Vol.127 No.9, pp.1407-1416-
dc.identifier.issn0008-543X-
dc.identifier.urihttps://hdl.handle.net/10371/189623-
dc.description.abstractBACKGROUND: In this open-label, international phase 2 study, the authors assessed the efficacy and safety of olmutinib in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) who had a confirmed T790M mutation and disease progression on previous epidermal growth factor receptor-tyrosine kinase inhibitor therapy. METHODS: Patients aged >= 20 years received once-daily oral olmutinib 800 mg continuously in 21-day cycles. The primary endpoint was the objective response rate (patients who had a confirmed best overall response of a complete or partial response), assessed by central review. Secondary endpoints included the disease control rate, the duration of objective response, progression-free survival, and overall survival. Adverse events were graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (version 4.03). RESULTS: Overall, 162 patients (median age, 63 years; women, >60%) were enrolled from 68 sites in 9 countries. At the time of database cutoff, 23.5% of enrolled patients remained on treatment. The median treatment duration was 6.5 months (range, 0.03-21.68 months). Overall, 46.3% of patients (95% CI, 38.4%-54.3%) had a confirmed objective response (all partial responses). The best overall response (the objective response rate regardless of confirmation) was 51.9% (84 patients; 95% CI, 43.9%-59.8%). The confirmed disease control rate for all patients was 86.4% ( 95% CI, 80.2%-91.3%). The median duration of objective response was 12.7 months (95% CI, 8.3-15.4 months). Estimated median progression-free survival was 9.4 months (95% CI, 6.9-12.3 months), and estimated median overall survival was 19.7 months (95% CI, 15.1 months to not reached). All patients experienced treatment-emergent adverse events, and 71.6% of patients had grade >= 3 treatment-emergent adverse events. CONCLUSIONS: Olmutinib has meaningful clinical activity and a manageable safety profile in patients with T790M-positive non-small cell lung cancer who received previous epidermal growth factor receptor-tyrosine kinase inhibitor therapy. Cancer 2020;0:1-10. (c) 2020 The Authors. Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.-
dc.language영어-
dc.publisherJohn Wiley & Sons Inc.-
dc.titleOlmutinib in T790M-positive non-small cell lung cancer after failure of first-line epidermal growth factor receptor-tyrosine kinase inhibitor therapy: A global, phase 2 study-
dc.typeArticle-
dc.identifier.doi10.1002/cncr.33385-
dc.citation.journaltitleCancer-
dc.identifier.wosid000606964500001-
dc.identifier.scopusid2-s2.0-85099224690-
dc.citation.endpage1416-
dc.citation.number9-
dc.citation.startpage1407-
dc.citation.volume127-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, Dong-Wan-
dc.contributor.affiliatedAuthorLee, Jong-Seok-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusACQUIRED-RESISTANCE-
dc.subject.keywordPlusII TRIAL-
dc.subject.keywordPlusEGFR-
dc.subject.keywordPlusGEFITINIB-
dc.subject.keywordPlusERLOTINIB-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordPlusAFATINIB-
dc.subject.keywordPlusMUTATION-
dc.subject.keywordPlusCARBOPLATIN-
dc.subject.keywordPlusPACLITAXEL-
dc.subject.keywordAuthorepidermal growth factor receptor-
dc.subject.keywordAuthornon-small cell lung cancer-
dc.subject.keywordAuthorolmutinib-
dc.subject.keywordAuthorT790M-
dc.subject.keywordAuthortyrosine kinase inhibitor-
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