Table 3.

Putative risk factors for failure and TTP

VariableNMedian TTP
(mo)
HR
(95% CI)
Log-rank
P value
Age ≥65 y     
 Y 31 30 0.88 (0.28-2.72) .819 
 N 18 NR 
≥4 prior lines of therapy     
 Y 27 30 2.03 (0.64-6.49) .222 
 N 22 NR 
F-refractory     
 Y 24 22 7.02 (1.73-28.45) .002 
 N 25 NR 
Bulky disease     
 Y 21 25 1.83 (0.61-5.49) .276 
 N 28 NR 
Rituximab combination studies     
 Y 12 NR 0.50 (0.12-2.21) .355 
 N 37 30 
Deletion 11q     
 Y 13 NR 0.34 (0.07-1.62) .154 
 N 36 30 
Deletion 17p     
 Y 21 30 1.24 (0.40-3.87) .709 
 N 28 NR 
Deletion 17p and/or TP53 mutation     
 Y 24 30 1.23 (0.34-4.41) .752 
 N 16 NR 
Complex karyotype     
 Y 11 16 6.61 (1.47-29.75) .005 
 N 19 NR 
VariableNMedian TTP
(mo)
HR
(95% CI)
Log-rank
P value
Age ≥65 y     
 Y 31 30 0.88 (0.28-2.72) .819 
 N 18 NR 
≥4 prior lines of therapy     
 Y 27 30 2.03 (0.64-6.49) .222 
 N 22 NR 
F-refractory     
 Y 24 22 7.02 (1.73-28.45) .002 
 N 25 NR 
Bulky disease     
 Y 21 25 1.83 (0.61-5.49) .276 
 N 28 NR 
Rituximab combination studies     
 Y 12 NR 0.50 (0.12-2.21) .355 
 N 37 30 
Deletion 11q     
 Y 13 NR 0.34 (0.07-1.62) .154 
 N 36 30 
Deletion 17p     
 Y 21 30 1.24 (0.40-3.87) .709 
 N 28 NR 
Deletion 17p and/or TP53 mutation     
 Y 24 30 1.23 (0.34-4.41) .752 
 N 16 NR 
Complex karyotype     
 Y 11 16 6.61 (1.47-29.75) .005 
 N 19 NR 

Univariate analyses of associations between putative risk factors for failure and TTP for all patients who received ≥400 mg/d of venetoclax. Variables were dichotomized: Y, present; N, absent; n, number with data for each variable group (where testing was not performed, data are not included).

NR, not reached.

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