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. 2016 Feb;22(2):248-257.
doi: 10.1016/j.bbmt.2015.08.024. Epub 2015 Aug 29.

Hematopoietic Cell Transplantation Outcomes in Monosomal Karyotype Myeloid Malignancies

Affiliations

Hematopoietic Cell Transplantation Outcomes in Monosomal Karyotype Myeloid Malignancies

Marcelo C Pasquini et al. Biol Blood Marrow Transplant. 2016 Feb.

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.

Keywords: Acute myeloid leukemia; Allogeneic transplantation; Monosomal karyotype; Myelodysplastic syndrome.

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Conflict of interest statement

Financial Disclosure Statement: There are no relevant conflicts of interest to disclose.

Figures

Figure 1
Figure 1
Cumulative incidence of disease relapse for AML in first complete remission(1A) and MDS (1B) and overall survival for AML in first complete remission (1C) and MDS (1D) after HCT,
Figure 1
Figure 1
Cumulative incidence of disease relapse for AML in first complete remission(1A) and MDS (1B) and overall survival for AML in first complete remission (1C) and MDS (1D) after HCT,
Figure 2
Figure 2
Overall survival for AML in first complete remission (2A) and MDS (2B) after HCT defined as chromosome 7 abnormalities with or without monosomal karyotype (MK+) and normal karyotype

Comment in

References

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