TY - JOUR
T1 - Prognostic implications of chromosome 17 abnormalities in the context of monosomal karyotype in patients with acute myeloid Leukemia and complex cytogenetics
AU - Nazha, Aziz
AU - Kantarjian, Hagop M.
AU - Bhatt, Vijaya R.
AU - Nogueras-Gonzalez, Graciela
AU - Cortes, Jorge E.
AU - Kadia, Tapan
AU - Garcia-Manero, Guillermo
AU - Abruzzo, Lynne
AU - Daver, Naval
AU - Pemmaraju, Naveen
AU - Quintas-Cardama, Alfonso
AU - Ravandi, Farhad
AU - Keating, Michael
AU - Borthakur, Gautam
PY - 2014/4
Y1 - 2014/4
N2 - Background Chromosome 17 abnormalities are associated with poor outcome in leukemias including AML. Recently, MK was introduced as an independent predictor of dismal outcome in AML. The additional prognostic effect of C17 abns in patients with MK in a CK background is not clear. Patients and Methods We conducted a retrospective analysis of 1086 patients with newly diagnosed AML treated between January 1998 and December 2007. Patients received treatment with one of the institution's first-line protocols. Results Four hundred eighty-three patients had CK. Among them, 370 patients (77%) had CK-MK, and 195 patients (53%) had CK-MK-C17 abns. Patients with CK-MK had significantly shorter OS rates compared with patients with CK without MK (4.4 vs. 8 months, respectively; P =.002). The median OS for patients with CK-C17 abns was shorter than for patients without C17 abns (4 vs. 6.1 months, respectively; P =.004). In a multivariate analysis, the presence of MK among patients with CK was identified as an independent prognostic marker for OS. In addition, presence of C17 abns had a significant negative effect on OS among patients with CK-MK (P =.04). Conclusion Among patients with CK-AML, MK was associated with poor outcomes. Additional presence of C17 abns further worsens the outcome in these particularly poor-risk patients with AML.
AB - Background Chromosome 17 abnormalities are associated with poor outcome in leukemias including AML. Recently, MK was introduced as an independent predictor of dismal outcome in AML. The additional prognostic effect of C17 abns in patients with MK in a CK background is not clear. Patients and Methods We conducted a retrospective analysis of 1086 patients with newly diagnosed AML treated between January 1998 and December 2007. Patients received treatment with one of the institution's first-line protocols. Results Four hundred eighty-three patients had CK. Among them, 370 patients (77%) had CK-MK, and 195 patients (53%) had CK-MK-C17 abns. Patients with CK-MK had significantly shorter OS rates compared with patients with CK without MK (4.4 vs. 8 months, respectively; P =.002). The median OS for patients with CK-C17 abns was shorter than for patients without C17 abns (4 vs. 6.1 months, respectively; P =.004). In a multivariate analysis, the presence of MK among patients with CK was identified as an independent prognostic marker for OS. In addition, presence of C17 abns had a significant negative effect on OS among patients with CK-MK (P =.04). Conclusion Among patients with CK-AML, MK was associated with poor outcomes. Additional presence of C17 abns further worsens the outcome in these particularly poor-risk patients with AML.
KW - AML
KW - Chromosome 17 abnormalities
KW - Complex karyotype
KW - Monosomal karyotype
UR - http://www.scopus.com/inward/record.url?scp=84896400386&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84896400386&partnerID=8YFLogxK
U2 - 10.1016/j.clml.2013.07.009
DO - 10.1016/j.clml.2013.07.009
M3 - Article
C2 - 24461514
AN - SCOPUS:84896400386
SN - 2152-2650
VL - 14
SP - 163
EP - 171
JO - Clinical Lymphoma
JF - Clinical Lymphoma
IS - 2
ER -