Barely Significant
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ASXL1 mutation as a surrogate marker in acute myeloid leukemia with myelodysplasia-related changes and normal karyotype.

Cancer Med · 2020 · PMC7286456 · PMID 32216059

2
hedged sentences
0.0720
closest p · 1.4× alpha
0.0720
boldest claim

The sentences

a clear trendP = .072so close (0.05 < p ≤ 0.1)
Differences in terms of overall survival between AML‐MRC ASXL1+ versus ASXL1− patients were found only in de novo AML‐MRC patients with intermediate‐risk karyotype (excluding MDS and MDS/MPN history and adverse‐risk karyotype), having ASXL1 + patients a worst outcome with a clear trend toward statistical association than ASXL1 −, HR = 2.9 P = .072 (Figure 3B ).

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showed a trendno p-value reported
In addition, ASXL1+ patients showed a trend toward a higher presence of megakaryocyte dysplasia (≥50%) in bone marrow.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.