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. 2021 Jun 1;106(6):1762-1766.
doi: 10.3324/haematol.2020.263319.

Structural aberrations are associated with poor survival in patients with clonal cytopenia of undetermined significance

Affiliations

Structural aberrations are associated with poor survival in patients with clonal cytopenia of undetermined significance

Stine U Mikkelsen et al. Haematologica. .

Abstract

Not available.

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Figures

Figure 1.
Figure 1.
Single nucleotide polymorphism- based array analysisdetected structural aberrations demarcate survival in patients with idiopathic cytopenia of undetermined significance but are not an independent adverse prognostic factor. Kaplan-Meier estimates of (A) overall survival and (B) progression- free survival of the group of idiopathic cytopenia of undetermined significance (ICUS) patients with copy number aberrations (CNA) or copy neutral loss of heterozygosity (CNLOH) (excluding loss of the Y chromosome; red curve) and the group of ICUS patients without CNA or CNLOH (black curve). (C) Forest plot of hazard ratios (HR) including 95% Confidence intervals (CI) for allcause mortality in multivariable analysis in ICUS patients (n=109 with complete data). Overall survival was measured from first bone marrow investigation (=inclusion) to death from any cause. Progression-free survival was measured from first bone marrow investigation to progression to a myeloid cancer or death from any cause. Annotated P-values are from two-sided log-rank tests. Severe anemia was defined as hemoglobin <100 g/L. Mutations were identified by targeted next generation sequencing using a 20- gene panel with a lower limit of detection at 2%.
Figure 2.
Figure 2.
In patienst with clonal cytopenia of undetermined significance, the presence of additional structural aberrations is associated with an increased hazard of all-cause mortality in univariable and multivariable analysis. (A) Kaplan-Meier estimates of overall survival of the group of clonal cytopenia of undetermined significance (CCUS) patients with copy number aberrations (CNA) or copy neutral loss of heterozygosity (CNLOH) (excluding loss of the Y chromosome; red curve) and the group of CCUS patients without CNA or CNLOH (black curve). (B) Forest plot of hazard ratios (HR) including 95% Confidence Intervals (CI) for all-cause mortality in multivariable analysis in CCUS patients (n=51 with complete data). Overall survival was measured from first bone marrow investigation (=inclusion) to death from any cause. Patients alive at the last date of follow-up were censored at that time. Annotated P-values are from two-sided log-rank tests. Severe anemia was defined as hemoglobin <100 g/L.

References

    1. Kwok B, Hall JM, Witte JS, et al. . MDS-associated somatic mutations and clonal hematopoiesis are common in idiopathic cytopenias of undetermined significance. Blood. 2015;126(21):2355-2361. - PMC - PubMed
    1. Malcovati L, Gallì A, Travaglino E, et al. . Clinical significance of somatic mutation in unexplained blood cytopenia. Blood. 2017; 129(25):3371-3378. - PMC - PubMed
    1. Kanagal-Shamanna R, Hodge JC, Tucker T, et al. . Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: an evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms. Cancer Genet. 2018;228-229:197-217. - PubMed
    1. Xu X, Bryke C, Sukhanova M, et al. . Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: an evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group. Cancer Genet. 2018;228-229:218-235. - PubMed
    1. Ronaghy A, Yang RK, Khoury JD, Kanagal-Shamanna R. Clinical applications of chromosomal microarray testing in myeloid malignancies. Curr Hematol Malig Rep. 2020;15(3):194-202. - PubMed

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