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Gilteritinib or Chemotherapy for Relapsed or Refractory FLT3-Mutated AML
Author(s) -
Alexander E. Perl,
Giovanni Martinelli,
Jorge E. Cortés,
Andreas Neubauer,
Ellin Berman,
Stefania Paolini,
Pau Montesinos,
Maria R. Baer,
Richard A. Larson,
Celalettin Üstün,
Francesco Fabbiano,
Harry P. Erba,
Antonio Di Stasi,
Robert K. Stuart,
Rebecca L. Olin,
Margaret Kasner,
Fabio Ciceri,
WenChien Chou,
Nikolai A. Podoltsev,
Christian Récher,
Hisayuki Yokoyama,
Naoko Hosono,
SungSoo Yoon,
JeHwan Lee,
Timothy S. Pardee,
Amir T. Fathi,
Chaofeng Liu,
Nahla Hasabou,
Xuan Liu,
Erkut Bahceci,
Mark J. Levis
Publication year - 2019
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1902688
Subject(s) - medicine , refractory (planetary science) , hazard ratio , chemotherapy , surgery , salvage therapy , gastroenterology , confidence interval , biology , astrobiology
Patients with relapsed or refractory acute myeloid leukemia (AML) with mutations in the FMS-like tyrosine kinase 3 gene ( FLT3 ) infrequently have a response to salvage chemotherapy. Gilteritinib is an oral, potent, selective FLT3 inhibitor with single-agent activity in relapsed or refractory FLT3 -mutated AML.

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