Table 1.

Combination therapies with venetoclax for patients with treatment-naive CLL

RegimenPhasenORR, %CRR, %MRD status, %Median follow-up, moPFSMedian DOROS
VO17  (NCT01685892) 1b 32 100 78 91: 3 mo after last obinutuzumab
91: 9 mo after last obinutuzumab
78: 12 mo after last obinutuzumab 
26.7 2 y = 90.6% NR NR 
VO18  30 NA NA 80 (24/29): end of obinutuzumab
86 (24/28): 6 mo after last obinutuzumab
89 (16/18): 9 mo after last obinutuzumab 
NA NA NA NA 
VO19  (NCT02242942) 216 84.7 49.5 75.5: 3 mo after venetoclax 28.1 2 y = 88.2% NR 2 y = 92% 
Venetoclax + ibrutinib26  (NCT02756897) 80 100* 96* 69: 18 mo of combination* 14.8 1 y = 98% NR 1 y = 99% 
Venetoclax + ibrutinib + obinutuzumab27  (NCT02427451) 25 84 32 83: end of obinutuzumab
95: 2 mo after last obinutuzumab 
24.2 NA NA NA 
RegimenPhasenORR, %CRR, %MRD status, %Median follow-up, moPFSMedian DOROS
VO17  (NCT01685892) 1b 32 100 78 91: 3 mo after last obinutuzumab
91: 9 mo after last obinutuzumab
78: 12 mo after last obinutuzumab 
26.7 2 y = 90.6% NR NR 
VO18  30 NA NA 80 (24/29): end of obinutuzumab
86 (24/28): 6 mo after last obinutuzumab
89 (16/18): 9 mo after last obinutuzumab 
NA NA NA NA 
VO19  (NCT02242942) 216 84.7 49.5 75.5: 3 mo after venetoclax 28.1 2 y = 88.2% NR 2 y = 92% 
Venetoclax + ibrutinib26  (NCT02756897) 80 100* 96* 69: 18 mo of combination* 14.8 1 y = 98% NR 1 y = 99% 
Venetoclax + ibrutinib + obinutuzumab27  (NCT02427451) 25 84 32 83: end of obinutuzumab
95: 2 mo after last obinutuzumab 
24.2 NA NA NA 

CRR, complete response rate; DOR, duration of response; NA, not available; NR, not reached.

*

Not reported by intention-to-treat population. As assessed in 26 available patients after 18 cycles of ibrutinib and venetoclax combination therapy.

As assessed by intention to treat.

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