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Data · dataset · 2026

<p>Mutation patterns and survival according to response to Aza/Ven.</p>

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<p>A. Concordance between G-banding and ELN 2022 cytogenetic risk classifications.

Description

Sankey diagram showing reclassification of patients (n = 53) from conventional G-banding–based cytogenetic risk groups (left) to ELN 2022 risk groups (right). Flow width is proportional to the number of cases.

Of 1 patient classified as favorable by G-banding, 1 remained favorable under ELN 2022. Of 30 patients classified as intermediate, 16 remained intermediate, 5 were reclassified as favorable, and 9 were reclassified as adverse. Genes involved in risk reclassification included <i>NPM1</i> for intermediate-to-favorable reclassification (n = 5), and <i>EZH2</i> (n = 2), <i>RUNX1</i> (n = 2), <i>SRSF2</i> (n = 2), <i>TP53</i> (n = 2), and <i>U2AF1</i> (n = 1) for intermediate-to-adverse reclassification.

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All 22 patients classified as adverse remained adverse under ELN 2022, resulting in 31 adverse cases in total. B. Overall survival according to response to first-line Aza/Ven. C. Treatment response according to gene mutation (n ≥ 2).

CR/CRi ratios were as follows: <i>IDH1</i> (100%, n = 3), <i>IDH2</i> (100%, n = 3), <i>FLT3-TKD</i> (83%, n = 6), <i>PTPN11</i> (80%, n = 5), <i>NRAS</i> (71%, n = 7), <i>CBL</i> (67%, n = 3), <i>FLT3-ITD</i> (63%, n = 8), <i>NPM1</i> (62%, n = 13), <i>SRSF2</i> (50%, n = 4), <i>EZH2</i> (50%, n = 2), <i>SETBP1</i> (50%, n = 2), <i>NF1</i> (50%, n = 4), <i>GATA2</i> (50%, n = 2), <i>TP53</i> (42%, n = 12), <i>RUNX1</i> (25%, n = 4), and <i>KRAS</i> (17%, n = 6).

Green indicates Type 1 mutations, purple indicates Type 2 mutations, and blue indicates other mutations. D. Distribution of treatment response (CR/CRi vs non-CR). CR/CRi (n = 52): type 1 (63%, n = 33), type 2 (15%, n = 8), others (21%, n = 11).

Non-CR (n = 38): type 1 (32%, n = 12), type 2 (42%, n = 16), others (26%, n = 10) (p = 0.0050). Aza, azacitidine; CR, complete remission; CRi, CR with incomplete hematologic recovery; ELN, European LeukemiaNet; Ven, venetoclax.</p>

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UCL Research Data Repositoryoai:figshare.com:article/340500639 d agoJSON v1
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