| Literature DB >> 26327629 |
Marcelo C Pasquini1, Mei-Jie Zhang2, Bruno C Medeiros3, Philippe Armand4, Zhen-Huan Hu5, Taiga Nishihori6, Mahmoud D Aljurf7, Görgün Akpek8, Jean-Yves Cahn9, Mitchell S Cairo10, Jan Cerny11, Edward A Copelan12, Abhinav Deol13, César O Freytes14, Robert Peter Gale15, Siddhartha Ganguly16, Biju George17, Vikas Gupta18, Gregory A Hale19, Rammurti T Kamble20, Thomas R Klumpp21, Hillard M Lazarus22, Selina M Luger23, Jane L Liesveld24, Mark R Litzow25, David I Marks26, Rodrigo Martino27, Maxim Norkin28, Richard F Olsson29, Betul Oran30, Attaphol Pawarode31, Michael A Pulsipher32, Muthalagu Ramanathan11, Ran Reshef23, Ayman A Saad33, Wael Saber5, Bipin N Savani34, Harry C Schouten35, Olle Ringdén36, Martin S Tallman37, Geoffrey L Uy38, William A Wood39, Baldeep Wirk40, Waleska S Pérez5, Minoo Batiwalla41, Daniel J Weisdorf42.
Abstract
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.Entities:
Keywords: Acute myeloid leukemia; Allogeneic transplantation; Monosomal karyotype; Myelodysplastic syndrome
Mesh:
Year: 2015 PMID: 26327629 PMCID: PMC4716890 DOI: 10.1016/j.bbmt.2015.08.024
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742