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. 2015 Jan 22;125(12):1922–1931. doi: 10.1182/blood-2014-08-596247

Table 3.

Association between clinical and biological variables and High-M phenotype in SMZL patients

Variables High-M phenotype Low-M phenotype Fisher’s exact test Pearson χ2
Notch pathway mutation 10/21 (48%) 7/46 (15%) .0072a .0047b
NOTCH2 mutation 8/21 (38%) 4/46 (9%) .0063a .0036b
IGHV1-02 usage 8/22 (36%) 8/65 (12%) .0225a .0118a
HCV status 2/26 (8%) 11/58 (19%) .3273d .1866d
High grade transformation 5/13 (38%) 0/47 (0%) .0002c <.0001c
Increased LDH 8/18 (44%) 11/44 (25%) .1445d .1317d
7q31.32 loss 12/28 (43%) 13/74 (18%) .0184a .0081a
17p loss 5/28 (18%) 11/74 (15%) .7631d .7108d
age <60 y 16/22 (73%) 60/85 (71%) 1.0000d .8437d
IILSS* 11/16 (69%) 19/39 (49%) .2374d .1754d
KM3 phenotype 33/33 (100%) 5/102 (5%) <.0001c <.0001c
KLF4 (cg07309102) 31/33 (94%) 9/101 (9%) <.0001c <.0001c
CACNB2 (cg01805540) 30/33 (91%) 18/101 (18%) <.0001c <.0001c
HTRA1 (cg25920792) 31/33 (94%) 11/101 (11%) <.0001c <.0001c

LDH, lactate dehydrogenase.

*

For IILSS, the comparison was high and intermediate value vs low value: a, P < .05; b, P < .005; c, P < .0005; d, borderline significance.