Hematopoietic Cell Transplantation Outcomes in Monosomal Karyotype Myeloid Malignancies.

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作者:Pasquini Marcelo C, Zhang Mei-Jie, Medeiros Bruno C, Armand Philippe, Hu Zhen-Huan, Nishihori Taiga, Aljurf Mahmoud D, Akpek Görgün, Cahn Jean-Yves, Cairo Mitchell S, Cerny Jan, Copelan Edward A, Deol Abhinav, Freytes César O, Gale Robert Peter, Ganguly Siddhartha, George Biju, Gupta Vikas, Hale Gregory A, Kamble Rammurti T, Klumpp Thomas R, Lazarus Hillard M, Luger Selina M, Liesveld Jane L, Litzow Mark R, Marks David I, Martino Rodrigo, Norkin Maxim, Olsson Richard F, Oran Betul, Pawarode Attaphol, Pulsipher Michael A, Ramanathan Muthalagu, Reshef Ran, Saad Ayman A, Saber Wael, Savani Bipin N, Schouten Harry C, Ringdén Olle, Tallman Martin S, Uy Geoffrey L, Wood William A Jr, Wirk Baldeep, Pérez Waleska S, Batiwalla Minoo, Weisdorf Daniel J
The presence of monosomal karyotype (MK+) in acute myeloid leukemia (AML) is associated with dismal outcomes. We evaluated the impact of MK+ in AML (MK+AML, n = 240) and in myelodysplastic syndrome (MDS) (MK+MDS, n = 221) on hematopoietic cell transplantation outcomes compared with other cytogenetically defined groups (AML, n = 3360; MDS, n = 1373) as reported to the Center for International Blood and Marrow Transplant Research from 1998 to 2011. MK+ AML was associated with higher disease relapse (hazard ratio, 1.98; P < .01), similar transplantation-related mortality (TRM) (hazard ratio, 1.01; P = .90), and worse survival (hazard ratio, 1.67; P < .01) compared with those outcomes for other cytogenetically defined AML. Among patients with MDS, MK+ MDS was associated with higher disease relapse (hazard ratio, 2.39; P < .01), higher TRM (hazard ratio, 1.80; P < .01), and worse survival (HR, 2.02; P < .01). Subset analyses comparing chromosome 7 abnormalities (del7/7q) with or without MK+ demonstrated higher mortality for MK+ disease in for both AML (hazard ratio, 1.72; P < .01) and MDS (hazard ratio, 1.79; P < .01). The strong negative impact of MK+ in myeloid malignancies was observed in all age groups and using either myeloablative or reduced-intensity conditioning regimens. Alternative approaches to mitigate disease relapse in this population are needed.

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