Gilteritinib or Chemotherapy for Relapsed or Refractory FLT3-Mutated AML

Oral use of the selective FLT3 kinase inhibitor gilteritinib in patients who had relapsed or refractory acute myeloid leukemia with FLT3 mutations led to a median overall survival of 9.3 months (vs. 5.6 months with standard chemotherapy) and complete remission with full or partial hematologic recove...

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Published inThe New England journal of medicine Vol. 381; no. 18; pp. 1728 - 1740
Main Authors Perl, Alexander E, Martinelli, Giovanni, Cortes, Jorge E, Neubauer, Andreas, Berman, Ellin, Paolini, Stefania, Montesinos, Pau, Baer, Maria R, Larson, Richard A, Ustun, Celalettin, Fabbiano, Francesco, Erba, Harry P, Di Stasi, Antonio, Stuart, Robert, Olin, Rebecca, Kasner, Margaret, Ciceri, Fabio, Chou, Wen-Chien, Podoltsev, Nikolai, Recher, Christian, Yokoyama, Hisayuki, Hosono, Naoko, Yoon, Sung-Soo, Lee, Je-Hwan, Pardee, Timothy, Fathi, Amir T, Liu, Chaofeng, Hasabou, Nahla, Liu, Xuan, Bahceci, Erkut, Levis, Mark J
Format Journal Article
LanguageEnglish
Published United States Massachusetts Medical Society 31.10.2019
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Summary:Oral use of the selective FLT3 kinase inhibitor gilteritinib in patients who had relapsed or refractory acute myeloid leukemia with FLT3 mutations led to a median overall survival of 9.3 months (vs. 5.6 months with standard chemotherapy) and complete remission with full or partial hematologic recovery in 34.0% of patients (vs. 15.3%).
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ISSN:0028-4793
1533-4406
1533-4406
DOI:10.1056/NEJMoa1902688