Barely Significant
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Myeloid Neoplasms With Erythroid Predominance and Excess Blasts in Young Adults Exhibit Distinct Genetic Profiles.

Eur J Haematol · 2025 · PMC12224554 · PMID 40370262

1
hedged sentence
0.1200
closest p · 2.4× alpha
0.1200
boldest claim

The sentences

did not reach statistical significancep = 0.12not close (p > 0.1)
In this population of young adults with AEML, the presence of UBTF ‐TD was associated with a decreased DFS compared to NPM1 ‐mutated patients and NPM1/UBTF ‐unmutated patients although it did not reach statistical significance (5y‐DFS: 15% [95% CI: 2.8%–80.4%], 58.2% [95% CI: 37.4%–90.5%] and 66.7% [95% CI: 46.6%–95.3%] respectively; p = 0.12) (Figure S2 ). 3.3 NPM1 ‐Mutated AEML Molecular Features Our cohort of AEML included 15 cases with NPM1 mutations, which represented the most frequent molecular lesion in young adults.

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