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김은희

Kim, Eunhee
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dc.citation.endPage 1747 -
dc.citation.number 18 -
dc.citation.startPage 1733 -
dc.citation.title NEW ENGLAND JOURNAL OF MEDICINE -
dc.citation.volume 373 -
dc.contributor.author Tiacci, E. -
dc.contributor.author Park, J. H. -
dc.contributor.author De Carolis, L. -
dc.contributor.author Chung, S. S. -
dc.contributor.author Broccoli, A. -
dc.contributor.author Scott, S. -
dc.contributor.author Zaja, F. -
dc.contributor.author Devlin, S. -
dc.contributor.author Pulsoni, A. -
dc.contributor.author Chung, Y. R. -
dc.contributor.author Cimminiello, M. -
dc.contributor.author Kim, Eunhee -
dc.contributor.author Rossi, D. -
dc.contributor.author Stone, R. M. -
dc.contributor.author Motta, G. -
dc.contributor.author Saven, A. -
dc.contributor.author Varettoni, M. -
dc.contributor.author Altman, J. K. -
dc.contributor.author Anastasia, A. -
dc.contributor.author Grever, M. R. -
dc.contributor.author Ambrosetti, A. -
dc.contributor.author Rai, K. R. -
dc.contributor.author Fraticelli, V. -
dc.contributor.author Lacouture, M. E. -
dc.contributor.author Carella, A. M. -
dc.contributor.author Levine, R. L. -
dc.contributor.author Leoni, P. -
dc.contributor.author Rambaldi, A. -
dc.contributor.author Falzetti, F. -
dc.contributor.author Ascani, S. -
dc.contributor.author Capponi, M. -
dc.contributor.author Martelli, M. P. -
dc.contributor.author Park, C. Y. -
dc.contributor.author Pileri, S. A. -
dc.contributor.author Rosen, N. -
dc.contributor.author Foa, R. -
dc.contributor.author Berger, M. F. -
dc.contributor.author Zinzani, P. L. -
dc.contributor.author Abdel-Wahab, O. -
dc.contributor.author Falini, B. -
dc.contributor.author Tallman, M. S. -
dc.date.accessioned 2023-12-22T00:39:01Z -
dc.date.available 2023-12-22T00:39:01Z -
dc.date.created 2016-08-02 -
dc.date.issued 2015-10 -
dc.description.abstract BACKGROUND BRAF V600E is the genetic lesion underlying hairy-cell leukemia. We assessed the safety and activity of the oral BRAF inhibitor vemurafenib in patients with hairy-cell leukemia that had relapsed after treatment with a purine analogue or who had disease that was refractory to purine analogues. METHODS We conducted two phase 2, single-group, multicenter studies of vemurafenib (at a dose of 960 mg twice daily) - one in Italy and one in the United States. The therapy was administered for a median of 16 weeks in the Italian study and 18 weeks in the U.S. study. Primary end points were the complete response rate (in the Italian trial) and the overall response rate (in the U.S. trial). Enrollment was completed (28 patients) in the Italian trial in April 2013 and is still open (26 of 36 planned patients) in the U.S. trial. RESULTS The overall response rates were 96% (25 of 26 patients who could be evaluated) after a median of 8 weeks in the Italian study and 100% (24 of 24) after a median of 12 weeks in the U.S. study. The rates of complete response were 35% (9 of 26 patients) and 42% (10 of 24) in the two trials, respectively. In the Italian trial, after a median follow-up of 23 months, the median relapse-free survival was 19 months among patients with a complete response and 6 months among those with a partial response; the median treatment-free survival was 25 months and 18 months, respectively. In the U.S. trial, at 1 year, the progression-free survival rate was 73% and the overall survival rate was 91%. Drug-related adverse events were usually of grade 1 or 2, and the events most frequently leading to dose reductions were rash and arthralgia or arthritis. Secondary cutaneous tumors (treated with simple excision) developed in 7 of 50 patients. The frequent persistence of phosphorylated ERK-positive leukemic cells in bone marrow at the end of treatment suggests bypass reactivation of MEK and ERK as a resistance mechanism. CONCLUSIONS A short oral course of vemurafenib was highly effective in patients with relapsed or refractory hairy-cell leukemia. -
dc.identifier.bibliographicCitation NEW ENGLAND JOURNAL OF MEDICINE, v.373, no.18, pp.1733 - 1747 -
dc.identifier.doi 10.1056/NEJMoa1506583 -
dc.identifier.issn 0028-4793 -
dc.identifier.scopusid 2-s2.0-84946032602 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/20161 -
dc.identifier.url http://www.nejm.org/doi/10.1056/NEJMoa1506583 -
dc.identifier.wosid 000363514100009 -
dc.language 영어 -
dc.publisher MASSACHUSETTS MEDICAL SOC -
dc.title Targeting Mutant BRAF in Relapsed or Refractory Hairy-Cell Leukemia -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus INHIBITOR DABRAFENIB -
dc.subject.keywordPlus MEK INHIBITION -
dc.subject.keywordPlus MELANOMA -
dc.subject.keywordPlus MUTATIONS -
dc.subject.keywordPlus ACTIVATION -
dc.subject.keywordPlus CANCER -
dc.subject.keywordPlus RAF -
dc.subject.keywordPlus VEMURAFENIB -
dc.subject.keywordPlus SURVIVAL -
dc.subject.keywordPlus CLADRIBINE -

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