Table 3.

Association between IGVH gene status and other prognostic factors

FactorMutated
N = 123
Unmutated N = 82Odds ratio
(95% CI)
P
Sex-male 49%  (60) 71%  (58) 2.5  (1.4, 4.6) .003 
Abnormal karyotype 60%  (74) 83%  (67) 3.2  (1.6, 6.3) .001  
Karyotype evolution present 18%  (19) 29%  (18) 1.9  (0.9, 3.9) .15   
Atypical morphology 18%  (21) 59%  (47) 6.6  (3.5, 12.7) < .001  
CD38 ≥ 30% 25%  (27) 72%  (44) 8.0  (3.9, 16.2) < .001  
Disease stage    < .001 
 A 93%  (114) 67%  (55) 1.0  
 B 2%  (3) 22%  (18) 12.4  (3.5, 44.0)  
 C 5%  (6) 11%  (9) 3.1  (1.1, 9.2)  
Chromosome 13 abnormal 53%  (64) 29%  (24) 0.4  (0.2, 0.7) .002  
Chromosome 12 abnormal 22%  (26) 45%  (35) 2.9  (1.6, 5.5) .001  
Chromosome 11 abnormal 8%  (9) 20%  (16) 3.1  (1.3, 7.4) .02  
Chromosome 17 abnormal 5%  (6) 14%  (9) 2.8  (1.0, 8.4) .09  
FactorMutated
N = 123
Unmutated N = 82Odds ratio
(95% CI)
P
Sex-male 49%  (60) 71%  (58) 2.5  (1.4, 4.6) .003 
Abnormal karyotype 60%  (74) 83%  (67) 3.2  (1.6, 6.3) .001  
Karyotype evolution present 18%  (19) 29%  (18) 1.9  (0.9, 3.9) .15   
Atypical morphology 18%  (21) 59%  (47) 6.6  (3.5, 12.7) < .001  
CD38 ≥ 30% 25%  (27) 72%  (44) 8.0  (3.9, 16.2) < .001  
Disease stage    < .001 
 A 93%  (114) 67%  (55) 1.0  
 B 2%  (3) 22%  (18) 12.4  (3.5, 44.0)  
 C 5%  (6) 11%  (9) 3.1  (1.1, 9.2)  
Chromosome 13 abnormal 53%  (64) 29%  (24) 0.4  (0.2, 0.7) .002  
Chromosome 12 abnormal 22%  (26) 45%  (35) 2.9  (1.6, 5.5) .001  
Chromosome 11 abnormal 8%  (9) 20%  (16) 3.1  (1.3, 7.4) .02  
Chromosome 17 abnormal 5%  (6) 14%  (9) 2.8  (1.0, 8.4) .09  
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