Table 2

Summary of TP53 abnormalities identified in CLL patients and their association with biologic and clinical variables

AbnormalityMonoallelic alterationsBiallelic alterations
Total 23 47 
Type of defect (n) del(17p) (3), mutation (20) del(17p)/mutation (42), mutation/mutation (5) 
Proportion of missense mutations, % 100 67* 
High risk: Rai stage III/IV (at the time of TP53 status examination), % (n) 48 (10/21) 67 (29/43) 
P .13 < .001 
Unmutated IgVH, % (n) 86 (18/21) 93 (41/44) 
P .025 .001 
11q deletion, % (n) 43 (10/23) 11 (5/47) 
P .014 .055 
AbnormalityMonoallelic alterationsBiallelic alterations
Total 23 47 
Type of defect (n) del(17p) (3), mutation (20) del(17p)/mutation (42), mutation/mutation (5) 
Proportion of missense mutations, % 100 67* 
High risk: Rai stage III/IV (at the time of TP53 status examination), % (n) 48 (10/21) 67 (29/43) 
P .13 < .001 
Unmutated IgVH, % (n) 86 (18/21) 93 (41/44) 
P .025 .001 
11q deletion, % (n) 43 (10/23) 11 (5/47) 
P .014 .055 

P = .003 (biallelic vs monoallelic alterations in relation to 11q deletion).

CLL indicates chronic lymphocytic leukemia.

*

In the subgroup del(17p)/mutation.

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