Barely Significant
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Genomic structural variations contribute to inform prognosis in patients with cytogenetically normal acute myeloid leukemia.

Blood Cancer J · 2026 · PMC13005009 · PMID 41792115

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0.0010
closest p · 0.0× alpha
0.0010
boldest claim

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highly significantP < 0.001actually significant
The difference remained highly significant after censoring at ASCT (9.7 months; 95%CI: 0-20.3, vs 54.5 months; 95%CI, 30.5-78.3; P < 0.001) (Supplementary Fig. 3a ).

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