In a univariable Cox model, the impact of LSC17 status on OS was significant in patients with NPM1 -mutated AML (HR, 2.71; 95% CI, 1.63-4.53; P = .0001) but did not reach statistical significance in patients with AML with wild-type NPM1 (HR, 1.35; 95% CI, 0.96-1.89; P = .08; Figure 3 A).
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LSC17 score complements genetics and measurable residual disease in acute myeloid leukemia: an ALFA study.
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