Table 1 Cox regression analysis of treatment-free survival in the whole cohort

From: KRAS, NRAS, and BRAF mutations are highly enriched in trisomy 12 chronic lymphocytic leukemia and are associated with shorter treatment-free survival

  

Univariable

 

Multivariable (n = 365)

N pts analyzed

HR (95% CI)

p-value

HR (95% CI)

p-value

male gender

442

0.97 (0.76–1.22)

0.8

−

−

age ≥ 65

441

0.97 (0.77–1.23)

0.8

−

−

Rai stage II–III–IV

434

2.60 (2.03–3.32)

<0.0001

2.59 (1.98–3.41)

<0.0001

CD49d positive (≥30%)

440

1.48 (1.13–1.92)

0.004

1.65 (1.22–2.23)

0.001

CD38 positive (≥30%)

439

1.13 (0.89–1.43)

0.3

−

−

ZAP-70 positive (≥20%)

389

1.44 (1.11–1.87)

0.005

n.i.

n.i.

IGHV unmutated

428

2.16 (1.66–2.8)

<0.0001

1.83 (1.37–2.45)

<0.0001

TP53 disrupted (del17p and/or TP53 mutated)

442

1.70 (1.24–2.32)

0.0008

1.46 (1.05–2.03)

0.024

NOTCH1 mutated

442

1.37 (1.08–1.73)

0.009

n.i.

n.i.

SF3B1 mutated

327

1.46 (0.90–2.38)

0.1

−

−

BIRC3 mutated

343

0.93 (0.65–1.34)

0.7

−

−

KRAS mutated

442

1.49 (0.96–2.30)

0.073

−

−

NRAS mutated

442

1.86 (0.99–3.50)

0.055

−

−

BRAF mutated

442

1.34 (0.75–2.40)

0.3

−

−

KRAS/NRAS mutated

442

1.54 (1.05–2.25)

0.025

1.56 (1.04–2.36)

0.033

  1. Factors with p-value <0.05 in univariable analysis were entered in the multivariable analysis
  2. HR hazard ratio, CI confidence interval, n.i. variables not included in the model after stepwise selection