Table 1

Main clinicobiological features of stereotyped subset #2 and non–subset #2/IGHV3-21 cases included in the survival analysis

Subset #2 (n = 212)Non–subset #2/ IGHV3-21 (n = 143)P
Male 132/254, 62% 87/183, 61% ns 
Age (median) 63.5 y 62.2 y ns 
Binet A 72/156, 46% 50/81, 61% .023 
U-CLL 86/212, 40% 84/143, 59% .0007 
CD38 expression 35/92, 38% 31/73, 42% ns 
ZAP70 expression 23/54, 43% 16/33, 48% ns 
del(13q) 50/81, 61% 27/51, 53% ns 
Trisomy 12 5/103, 5% 5/65, 8% ns 
del(11q) 23/109, 21% 10/70, 14% ns 
del(17p) 4/103, 4% 3/69, 4% ns 
TTFT 22 mo 60 mo .001 
TTFT (M-CLL) 23 mo 154 mo <.0001 
TTFT (U-CLL) 19 mo 30 mo ns 
Subset #2 (n = 212)Non–subset #2/ IGHV3-21 (n = 143)P
Male 132/254, 62% 87/183, 61% ns 
Age (median) 63.5 y 62.2 y ns 
Binet A 72/156, 46% 50/81, 61% .023 
U-CLL 86/212, 40% 84/143, 59% .0007 
CD38 expression 35/92, 38% 31/73, 42% ns 
ZAP70 expression 23/54, 43% 16/33, 48% ns 
del(13q) 50/81, 61% 27/51, 53% ns 
Trisomy 12 5/103, 5% 5/65, 8% ns 
del(11q) 23/109, 21% 10/70, 14% ns 
del(17p) 4/103, 4% 3/69, 4% ns 
TTFT 22 mo 60 mo .001 
TTFT (M-CLL) 23 mo 154 mo <.0001 
TTFT (U-CLL) 19 mo 30 mo ns 

del(13q): isolated deletion of chromosome 13q; ns: nonsignificant. P values in bold indicate statistically significant differences.

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