Table 1 Comparison of clinicopathological features of 156 CLL/SLL patients with or without MYD88 mutations.

From: Clinicopathological characterization of chronic lymphocytic leukemia with MYD88 mutations: L265P and non-L265P mutations are associated with different features

Features

WT (n = 100)

A (L265P, n = 38)

B (Non-L265P, n = 18)

P-value

WT vs. A

WT vs. B

A vs. B

Age @ dx

 Median

 Range

58.5

55

61

0.0077

NS

0.0071

(30–81)

(23–73)

(51–79)

M:F

2.2:1 (69:31)

4.4:1 (31:7)

2:1 (12:6)

NS

NS

NS

Rai stage III–IV @ dx

14% (13/91)

5% (2/38)

6% (1/16)

NS

NS

NS

1° or 2° relative with CLL

12% (10/83)

11% (4/35)

13% (2/15)

NS

NS

NS

ALC, × 109/L

 Median

 Range

16.6

13.4

22.3

NS

NS

NS

(1.3–328.6)

(2.0–238.8)

(0.3–90.8)

Serum Paraprotein +

9% (9/100)

11% (4/38)

6% (1/18)

NS

NS

NS

Elevated β2-microglobulin

62% (53/85)

38% (14/37)

56% (10/18)

0.0173

NS

NS

CD38+

47% (47/100)

16% (6/38)

17% (3/18)

0.0008a

0.0195

NS

ZAP-70+

68% (65/95)

23% (8/35)

53% (9/17)

<0.0001a

NS

0.0565

Mutated IGHV

39% (34/87)

97% (35/36)

63% (10/16)

<0.0001a

NS

0.0022

  1. CLL/SLL chronic lymphocytic leukemia/small lymphocytic lymphoma, WT wild-type, NS nonsignificant, ALC absolute lymphocyte count. The P-values close to or ≤0.05 are shown in bold with values ≤0.05 in italics as well.
  2. aStatistically significant after the Bonferroni correction for multiple testing (P ≤ 0.05/30 = 0.0017).