TY - JOUR
T1 - Factors associated with risk of central nervous system relapse in patients with non-core binding factor acute myeloid leukemia
AU - Jabbour, Elias
AU - Guastad Daver, Naval
AU - Short, Nicholas James
AU - Huang, Xuelin
AU - Chen, Hsiang Chun
AU - Maiti, Abhishek
AU - Ravandi, Farhad
AU - Cortes, Jorge
AU - Abi Aad, Simon
AU - Garcia-Manero, Guillermo
AU - Estrov, Zeev
AU - Kadia, Tapan
AU - O'Brien, Susan
AU - Dabaja, Bouthaina
AU - Bueso-Ramos, Carlos
AU - Strati, Paolo
AU - Bivins, Carol
AU - Pierce, Sherry
AU - Kantarjian, Hagop
N1 - Publisher Copyright:
© 2017 Wiley Periodicals, Inc.
PY - 2017/9
Y1 - 2017/9
N2 - Central nervous system (CNS) relapse is uncommon in patients with acute myeloid leukemia (AML) with the use of high-dose cytarabine containing chemotherapy regimens. The clinical and molecular features associated with a higher risk of CNS relapse are not well defined. We assessed the incidence and outcome of CNS relapses among 1245 patients with relapsed/refractory AML referred to our institution between 2000 and 2014. CNS leukemia relapse was observed in 51 patients (4.1%). Using a multivariate regression model and after adjusting for age, FLT3-ITD mutation (OR = 2.33; P =.02) and elevated LDH (>1000 IU/L, OR = 1.99; P =.04) were independent predictive factors for CNS relapse. Patients under 64 years of age with 0, 1, or 2 baseline adverse features had a probability of 3.8%, 7.0%-8.0%, and 13.9% for developing CNS disease, respectively. Our study identifies patients with AML at higher risk for CNS relapse in whom prophylactic CNS therapy may be warranted.
AB - Central nervous system (CNS) relapse is uncommon in patients with acute myeloid leukemia (AML) with the use of high-dose cytarabine containing chemotherapy regimens. The clinical and molecular features associated with a higher risk of CNS relapse are not well defined. We assessed the incidence and outcome of CNS relapses among 1245 patients with relapsed/refractory AML referred to our institution between 2000 and 2014. CNS leukemia relapse was observed in 51 patients (4.1%). Using a multivariate regression model and after adjusting for age, FLT3-ITD mutation (OR = 2.33; P =.02) and elevated LDH (>1000 IU/L, OR = 1.99; P =.04) were independent predictive factors for CNS relapse. Patients under 64 years of age with 0, 1, or 2 baseline adverse features had a probability of 3.8%, 7.0%-8.0%, and 13.9% for developing CNS disease, respectively. Our study identifies patients with AML at higher risk for CNS relapse in whom prophylactic CNS therapy may be warranted.
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U2 - 10.1002/ajh.24799
DO - 10.1002/ajh.24799
M3 - Article
C2 - 28556489
AN - SCOPUS:85025071097
SN - 0361-8609
VL - 92
SP - 924
EP - 928
JO - American Journal of Hematology
JF - American Journal of Hematology
IS - 9
ER -