Figure 1.
Figure 1. Variant allele frequency of mutations and course of platelet count prior to and during PEM therapy. (A) Variant allele frequency of single-nucleotide variants detected in IDH1, IDH2, ASXL1, RUNX1, and STAG2 in the patient before and during treatment with PEM. Analyses were done using published methods (panel next-generation sequencing analysis for 54 mutations; Trusight Myeloid Panel) including targeted ultradeep analysis for IDH1 and IDH2 with a sensitivity down to 0.1%.19 (B) After diagnosis of MDS EB-1, the patient presented with persistent thrombocytopenia. Two months after PEM treatment initiation, platelet counts increased from 34 Gpt/L to 81 Gpt/L. The course was complicated by a PEM-associated pneumonitis at ∼5 months after the start of therapy. During this period, PEM was stopped for 8 weeks, and the patient lost his platelet response subsequently. Response was regained after reintroduction of therapy. sAML, secondary AML.

Variant allele frequency of mutations and course of platelet count prior to and during PEM therapy. (A) Variant allele frequency of single-nucleotide variants detected in IDH1, IDH2, ASXL1, RUNX1, and STAG2 in the patient before and during treatment with PEM. Analyses were done using published methods (panel next-generation sequencing analysis for 54 mutations; Trusight Myeloid Panel) including targeted ultradeep analysis for IDH1 and IDH2 with a sensitivity down to 0.1%.19  (B) After diagnosis of MDS EB-1, the patient presented with persistent thrombocytopenia. Two months after PEM treatment initiation, platelet counts increased from 34 Gpt/L to 81 Gpt/L. The course was complicated by a PEM-associated pneumonitis at ∼5 months after the start of therapy. During this period, PEM was stopped for 8 weeks, and the patient lost his platelet response subsequently. Response was regained after reintroduction of therapy. sAML, secondary AML.

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