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Table 2 Cox regression analyses of variables for OS and LFS in whole-cohort-AML among TCGA cohort

From: BCL2 overexpression: clinical implication and biological insights in acute myeloid leukemia

Variables

OS

LFS

Univariate analysis

Multivariate analysis

Univariate analysis

Multivariate analysis

HR (95% CI)

P

HR (95% CI)

P

HR (95% CI)

P

HR (95% CI)

P

BCL2 expression

1.000 (1.000–1.000)

0.185

1.000 (1.000–1.000)

0.761

1.000 (1.000–1.000)

0.356

  

Age

1.040 (1.027–1.054)

0.000

1.027 (1.011–1.042)

0.001

1.035 (1.022–1.048)

0.000

1.027 (1.013–1.041)

0.000

WBC

1.003 (0.999–1.006)

0.119

1.007 (1.003–1.012)

0.001

1.003 (1.000–1.006)

0.091

1.003 (1.000–1.006)

0.040

Karyotype risk

1.854 (1.465–2.346)

0.000

2.208 (1.591–3.063)

0.000

1.829 (1.448–2.311)

0.000

2.065 (1.593–2.676)

0.000

Treatment regimens

0.551 (0.389–0.780)

0.001

0.441 (0.284–0.687)

0.000

0.615 (0.434–0.871)

0.006

0.546 (0.366–0.815)

0.003

FLT3 mutations

1.269 (0.869–1.852)

0.217

  

1.254 (0.859–1.829)

0.241

  

NPM1 mutations

1.220 (0.837–1.778)

0.301

  

1.268 (0.869–1.848)

0.218

  

CEBPA mutations

0.913 (0.464–1.796)

0.792

  

1.053 (0.535–2.073)

0.881

  

DNMT3A mutations

1.615 (1.104–2.362)

0.014

1.472 (0.951–2.279)

0.083

1.511 (1.035–2.206)

0.033

1.302 (0.860–1.973)

0.212

IDH1 mutations

0.843 (0.466–1.527)

0.574

  

0.890 (0.492–1.611)

0.700

  

IDH2 mutations

1.113 (0.649–1.910)

0.697

  

0.987 (0.576–1.691)

0.963

  

TET2 mutations

0.953 (0.514–1.767)

0.879

  

0.945 (0.510–1.751)

0.857

  

RUNX1 mutations

1.853 (1.077–3.186)

0.026

1.692 (1.137–2.518)

0.009

1.644 (0.959–2.817)

0.071

1.322 (0.912–1.916)

0.141

TP53 mutations

3.687 (2.144–6.339)

0.000

2.379 (1.211–4.673)

0.012

3.257 (1.912–5.549)

0.000

1.642 (0.904–2.984)

0.103

  1. OS overall survival, LFS leukemia-free survival, HR hazard ratio, CI confidence interval, WBC white blood cells. Variables in multivariate analysis including BCL2 expression, age, WBC, karyotype (favorable vs. intermediate vs. poor), treatment regimens (without/with HSCT) and gene mutations (mutant vs. wild-type)