Table 3.

Patient disposition among patients with higher-risk CLL

ParameterTN CLL (n = 320)R/R CLL (n = 488) Total (N = 808)
Follow-up, median (range), mo 59.1 (1-82) 44.3 (0-88) 49.1 (0-88) 
Patients remaining on treatment, n (%) 164 (51) 131 (27) 295 (37) 
Reasons for treatment discontinuation, n (%)    
Progressive disease 26 (8) 149 (31) 175 (22) 
Adverse event 44 (14) 81 (17) 125 (15) 
Study terminated by sponsor 42 (13) 74 (15) 116 (14) 
Death 11 (3) 18 (4) 29 (4) 
Lost to follow-up 2 (0.6) 1 (0.2) 3 (0.4) 
Richter transformation 1 (0.3) 2 (0.4) 3 (0.4) 
Other  30 (9) 32 (7) 62 (8) 
ParameterTN CLL (n = 320)R/R CLL (n = 488) Total (N = 808)
Follow-up, median (range), mo 59.1 (1-82) 44.3 (0-88) 49.1 (0-88) 
Patients remaining on treatment, n (%) 164 (51) 131 (27) 295 (37) 
Reasons for treatment discontinuation, n (%)    
Progressive disease 26 (8) 149 (31) 175 (22) 
Adverse event 44 (14) 81 (17) 125 (15) 
Study terminated by sponsor 42 (13) 74 (15) 116 (14) 
Death 11 (3) 18 (4) 29 (4) 
Lost to follow-up 2 (0.6) 1 (0.2) 3 (0.4) 
Richter transformation 1 (0.3) 2 (0.4) 3 (0.4) 
Other  30 (9) 32 (7) 62 (8) 

R/R data set includes acalabrutinib plus obinutuzumab data from the CL-003 study in addition to the acalabrutinib monotherapy data from the CL-001, ELEVATE-R/R, and ASCEND studies.

Other includes physician decision (TN, n = 11; R/R, n = 15), withdrawal of consent (TN, n = 5; R/R, n = 11), pregnancy (TN, n = 1; R/R, n = 0), and other (TN, n = 13; R/R, n = 6).

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