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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
DC Field | Value | Language |
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dc.contributor.author | Park, Keunchil | - |
dc.contributor.author | Janne, Pasi A. | - |
dc.contributor.author | Kim, Dong-Wan | - |
dc.contributor.author | Han, Ji-Youn | - |
dc.contributor.author | Wu, Ming-Fang | - |
dc.contributor.author | Lee, Jong-Seok | - |
dc.contributor.author | Kang, Jin-Hyoung | - |
dc.contributor.author | Lee, Dae Ho | - |
dc.contributor.author | Cho, Byoung Chul | - |
dc.contributor.author | Yu, Chong-Jen | - |
dc.contributor.author | Pang, Yong Kek | - |
dc.contributor.author | Felip, Enriqueta | - |
dc.contributor.author | Kim, Hyunjin | - |
dc.contributor.author | Baek, Eunhye | - |
dc.contributor.author | Noh, Young Su | - |
dc.date.accessioned | 2023-03-20T08:54:27Z | - |
dc.date.available | 2023-03-20T08:54:27Z | - |
dc.date.created | 2021-07-06 | - |
dc.date.created | 2021-07-06 | - |
dc.date.created | 2021-07-06 | - |
dc.date.issued | 2021-05 | - |
dc.identifier.citation | Cancer, Vol.127 No.9, pp.1407-1416 | - |
dc.identifier.issn | 0008-543X | - |
dc.identifier.uri | https://hdl.handle.net/10371/189623 | - |
dc.description.abstract | BACKGROUND: 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.language | 영어 | - |
dc.publisher | John Wiley & Sons Inc. | - |
dc.title | 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 | - |
dc.type | Article | - |
dc.identifier.doi | 10.1002/cncr.33385 | - |
dc.citation.journaltitle | Cancer | - |
dc.identifier.wosid | 000606964500001 | - |
dc.identifier.scopusid | 2-s2.0-85099224690 | - |
dc.citation.endpage | 1416 | - |
dc.citation.number | 9 | - |
dc.citation.startpage | 1407 | - |
dc.citation.volume | 127 | - |
dc.description.isOpenAccess | Y | - |
dc.contributor.affiliatedAuthor | Kim, Dong-Wan | - |
dc.contributor.affiliatedAuthor | Lee, Jong-Seok | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.subject.keywordPlus | ACQUIRED-RESISTANCE | - |
dc.subject.keywordPlus | II TRIAL | - |
dc.subject.keywordPlus | EGFR | - |
dc.subject.keywordPlus | GEFITINIB | - |
dc.subject.keywordPlus | ERLOTINIB | - |
dc.subject.keywordPlus | CHEMOTHERAPY | - |
dc.subject.keywordPlus | AFATINIB | - |
dc.subject.keywordPlus | MUTATION | - |
dc.subject.keywordPlus | OSIMERTINIB | - |
dc.subject.keywordPlus | CARBOPLATIN | - |
dc.subject.keywordAuthor | epidermal growth factor receptor | - |
dc.subject.keywordAuthor | non-small cell lung cancer | - |
dc.subject.keywordAuthor | olmutinib | - |
dc.subject.keywordAuthor | T790M | - |
dc.subject.keywordAuthor | tyrosine kinase inhibitor | - |
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