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. 2024 Nov 1;109(11):3785-3789.
doi: 10.3324/haematol.2024.285359.

FLT3 inhibitors potentially improve response rates in acute myeloid leukemia harboring t(6;9)(DEK::NUP214): the Mayo Clinic experience

Affiliations

FLT3 inhibitors potentially improve response rates in acute myeloid leukemia harboring t(6;9)(DEK::NUP214): the Mayo Clinic experience

Clifford M Csizmar et al. Haematologica. .
No abstract available

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Figures

Figure 1.
Figure 1.
Overall survival in t(6;9)(DEK::NUP214) acute myeloid leukemia and compared to European Leukemia Network risk groups. (A) The median overall survival (mOS) of the entire cohort. (B-F) mOS of fms-like tyrosine kinase 3 (FLT3) wild-type versus FLT3 internal tandem duplications (FLT3-ITD) cases (B); FLT3-ITD-positive cases receiving a FLT3 inhibitor (FLT3i) versus those that did not (C); t(6;9) acute myeloid leukemia (AML) patients undergoing allogeneic hematopoietic cell transplantation (alloHCT) versus those who did not (D); cases with wild-type FLT3 who underwent allogeneic hematopoietic cell transplantation (alloHCT) versus those who did not (E); and those with a FLT3-ITD mutation who underwent alloHCT compared to those who did not (F). (G) Comparison of OS in the t(6;9) AML cohort versus the ELN favorable, intermediate, and adverse-risk groups. (H) Comparison of OS in the t(6;9) AML subset who underwent alloHCT versus the European Leukemia Network (ELN) favorable, intermediate, and adverse-risk groups who also underwent alloHCT. (I) Comparison of OS in the t(6;9) AML cohort versus age-restricted subgroups of the comparison cohort; the median (range) ages of the 3 subgroups are 38 (18-55), 50 (18-60), and 56 (18-65) years (y), respectively. In (G-I), P values depict the comparison between the t(6;9) AML cohort and the color-matched subgroup of the comparison cohort. All survival times are denoted as median (95% confidence interval) in months (mo).

References

    1. Döhner H, Wei AH, Appelbaum FR, et al. . Diagnosis and management of AML in adults: 2022 ELN recommendations from an international expert panel. Blood. 2022;140(12):1345-1377.. - PubMed
    1. Slovak ML, Gundacker H, Bloomfield CD, et al. . A retrospective study of 69 patients with t(6;9)(p23;q34) AML emphasizes the need for a prospective, multicenter initiative for rare ‘poor prognosis’ myeloid malignancies. Leukemia. 2006;20(7):1295-1297. - PubMed
    1. Fang H, Yabe M, Zhang X, et al. . Myelodysplastic syndrome with t(6;9)(p22;q34.1)/DEK-NUP214 better classified as acute myeloid leukemia? A multicenter study of 107 cases. Mod Pathol. 2021;34(6):1143-1152. - PubMed
    1. Oyarzo MP, Lin P, Glassman A, Bueso-Ramos CE, Luthra R, Medeiros LJ. Acute myeloid leukemia with t(6;9)(p23;q34) is associated with dysplasia and a high frequency of flt3 gene mutations. Am J Clin Pathol. 2004;122(3):348-358. - PubMed
    1. Visconte V, Shetty S, Przychodzen B, et al. . Clinicopathologic and molecular characterization of myeloid neoplasms with isolated t(6;9)(p23;q34). Int J Lab Hematol. 2017;39(4):409-417. - PMC - PubMed

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