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Table 3 Univariate and multivariate analyses for clinical characteristics of EFS and OS in adult AML patients

From: Single-cell transcriptomics reveals multiple chemoresistant properties in leukemic stem and progenitor cells in pediatric AML

TCGA cohort (n = 79)

Univariate

Multivariate

Variable

EFS

HR (95% CI)

EFS

p.value

OS

HR (95% CI)

OS

p.value

EFS

HR (95% CI)

EFS

p.value

OS

HR (95% CI)

OS

p.value

Age > 60

1.93 (1.18–3.17)

0.009***

2.24 (1.32–3.81)

0.003***

1.45 (0.846–2.47)

0.178

1.58 (0.883–2.82)

0.124

BM blast > 70%

1.54 (0.804–2.96)

0.192

1.48 (0.747–2.94)

0.260

    

CD69+ HSC-like% (high vs low)

2.47 (1.5–4.07)

0.000***

2.36 (1.39–4.02)

0.001***

1.85 (1.04–3.27)

0.035**

2.1 (1.17–3.76)

0.013**

LSC score (high vs low)

2.87 (1.72–4.81)

0.000***

2.47 (1.44–4.23)

0.001***

2.5 (1.34–4.66)

0.004***

2.11 (1.12–3.98)

0.021**

Gender (male vs female)

0.988 (0.604–1.62)

0.962

0.943 (0.56–1.59)

0.824

    

Cytogenetic Risk Favorable

0.606 (0.261–1.41)

0.243

0.514 (0.205–1.29)

0.157

    

Cytogenetic Risk Intermediate/Normal

1.1 (0.648–1.88)

0.719

1.22 (0.689–2.16)

0.495

    

Cytogenetic Risk Poor

1.21 (0.668–2.2)

0.529

1.18 (0.624–2.25)

0.606

    

Molecular Risk Good

0.606 (0.261–1.41)

0.243

0.514 (0.205–1.29)

0.157

    

Molecular Risk Intermediate

0.958 (0.575–1.6)

0.870

0.833 (0.486–1.43)

0.504

    

Molecular Risk Poor

1.39 (0.806–2.41)

0.234

1.87 (1.05–3.33)

0.033**

1.13 (0.625–2.04)

0.689

1.88 (1.01–3.47)

0.045**

cytogenetic BCR-ABL1

12.9 (2.75–60.1)

0.001***

1.73 (0.237–12.7)

0.588

    

cytogenetic CBFB-MYH11

0.847 (0.307–2.34)

0.749

0.603 (0.188–1.94)

0.395

    

cytogenetic Complex

1.1 (0.439–2.74)

0.844

1.6 (0.636–4.02)

0.318

    

cytogenetic Intermediate Risk Abnormality

1.56 (0.788–3.1)

0.201

1.52 (0.741–3.13)

0.252

    

cytogenetic MLL, poor risk

0.826 (0.202–3.38)

0.791

1.03 (0.25–4.23)

0.969

    

cytogenetic MLL, t(9;11)

2.55 (0.345–18.8)

0.360

4.01 (0.533–30.1)

0.177

    

cytogenetic Normal

0.843 (0.514–1.38)

0.497

0.798 (0.471–1.35)

0.399

    

cytogenetic Poor Risk Abnormality

1.13 (0.407–3.11)

0.819

1.57 (0.564–4.34)

0.389

    

cytogenetic RUNX1-RUNX1T1

0.41 (0.1–1.68)

0.215

0.463 (0.113–1.9)

0.285

    

FLT3-ITD

1.41 (0.828–2.4)

0.206

1.12 (0.628–2.01)

0.693

    

FLT3-PM

2.05 (0.929–4.53)

0.075*

2.71 (1.2–6.08)

0.016**

    

CEBPA mutation

0.663 (0.241–1.83)

0.427

0.708 (0.256–1.96)

0.507

    

DNMT3A/B mutation

1.54 (0.898–2.64)

0.117

2.13 (1.22–3.74)

0.008***

    

NPM1 mutation

0.839 (0.503–1.4)

0.502

0.765 (0.443–1.32)

0.336

    

RUNX1 mutation

1.39 (0.552–3.51)

0.484

1.89 (0.742–4.84)

0.181

    

TP53 mutation

2.34 (0.846–6.47)

0.101

3.62 (1.29–10.2)

0.015**

    

WT1 mutation

0.988 (0.45–2.17)

0.977

0.733 (0.314–1.71)

0.474

    

SCT

0.642 (0.392–1.05)

0.078*

0.483 (0.284–0.822)

0.007***

0.497 (0.282–0.874)

0.015**

0.353 (0.19–0.657)

0.001***

  1. Factors with P < 0.10 in the univariate analyses were subjected to multivariate analysis. HR and CI represent hazard ratio and confidence interval respectively
  2. *p < 0.10
  3. **p < 0.05
  4. ***p < 0.01