Table 1

Clinical and genetic characterization of CLL samples without 17p deletion stratified by miR-34a expression

CharacteristicmiR-34a lowmiR-34a highP
VH unmutated 10 15  
VH mutated 17 n.s. 
13q- single 16 n.s. 
Trisomy 12 n.s. 
11q- n.s. 
Normal/other n.s. 
TP53 mutation  
TP53 wild-type 11 n.s.* 
Prior therapy  
No prior therapy 24 .052 
F-refractory  
F-sensitive or no treatment 30 < .002 
p53/p21 dysfunctional FACS 12  
Normal p21/p53 induction 29 < .001 
Viability after 5Gy (48 hours median) 68% 45% .04 
CharacteristicmiR-34a lowmiR-34a highP
VH unmutated 10 15  
VH mutated 17 n.s. 
13q- single 16 n.s. 
Trisomy 12 n.s. 
11q- n.s. 
Normal/other n.s. 
TP53 mutation  
TP53 wild-type 11 n.s.* 
Prior therapy  
No prior therapy 24 .052 
F-refractory  
F-sensitive or no treatment 30 < .002 
p53/p21 dysfunctional FACS 12  
Normal p21/p53 induction 29 < .001 
Viability after 5Gy (48 hours median) 68% 45% .04 

Distribution of clinical and genetic profile of CLL samples stratified by miR-34a expression. Groupwise comparisons were performed by Fisher exact test. Viability was compared using Student t test. Low miR-34a group includes cases with expression of miR-34a below median for basal and induced (5Gy) value. n.s. indicates not significant.

*

The majority of cases with high miR-34a expression were not tested for TP53 mutation (22/33 cases) but, based on their FACS profiles, are unlikely to have TP53 mutations.

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