Table 1.

Clinicopathological variables associated with PFS after BTKi initiation

Pre-BTKi variableNo. of patientsAssociation with PFS after BTKi initiation
HR (95% CI)Log-rank P
Age ≥65 y  2.03 (0.23-17.7) .515 
 Y 20   
 N 
≥4 prior lines of therapy  0.38 (0.11-1.40) .132 
 Y 17   
 N 
Fludarabine refractory  0.60 (0.18-2.04) .416 
 Y 15   
 N 
Bulky adenopathy (>5 cm)  NA NA 
 Y   
 N 19 
NOTCH1 mutation  0.67 (0.08-5.52) .698 
 Y   
 N 16 
IgHV unmutated  NA NA 
 Y 13   
 N 
del(17p) and/or TP53 mutation  2.24 (0.42-11.98) .332 
 Y 16   
 N 
CK  0.69 (0.17-2.81) .600 
 Y 13   
 N 
BTKi post-RT*  0.92 (0.25-3.43) .898 
 Y   
 N 18 
CR or uMRD to venetoclax  0.15 (0.02-1.08) .029 
 Y   
 N 15 
≥24 mo on venetoclax  0.31 (0.09-1.03) .044 
 Y 14   
 N 
BCL2 G101V  0.24 (0.05-1.16) .054 
 Y   
 N 11 
Pre-BTKi variableNo. of patientsAssociation with PFS after BTKi initiation
HR (95% CI)Log-rank P
Age ≥65 y  2.03 (0.23-17.7) .515 
 Y 20   
 N 
≥4 prior lines of therapy  0.38 (0.11-1.40) .132 
 Y 17   
 N 
Fludarabine refractory  0.60 (0.18-2.04) .416 
 Y 15   
 N 
Bulky adenopathy (>5 cm)  NA NA 
 Y   
 N 19 
NOTCH1 mutation  0.67 (0.08-5.52) .698 
 Y   
 N 16 
IgHV unmutated  NA NA 
 Y 13   
 N 
del(17p) and/or TP53 mutation  2.24 (0.42-11.98) .332 
 Y 16   
 N 
CK  0.69 (0.17-2.81) .600 
 Y 13   
 N 
BTKi post-RT*  0.92 (0.25-3.43) .898 
 Y   
 N 18 
CR or uMRD to venetoclax  0.15 (0.02-1.08) .029 
 Y   
 N 15 
≥24 mo on venetoclax  0.31 (0.09-1.03) .044 
 Y 14   
 N 
BCL2 G101V  0.24 (0.05-1.16) .054 
 Y   
 N 11 

Bold font indicates significance.

CI, confidence interval; CR, complete response; HR, hazard ratio; IgHV, immunoglobulin heavy chain variable region; NA, not applicable; RT, Richter transformation.

*

Patients receiving BTKi therapy for progressive CLL after treatment for RT on venetoclax with salvage chemotherapy ± autologous SCT.

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