Table 1.

Association of RDI with treatment outcome and patients' characteristics

Impact of obinutuzumab RDI reduction >20% on outcome
CharacteristicOverall (n = 130)RDI reduction of obinutuzumab doseP value*
>20% (n = 20)≤20% (n = 110)
ORR, n (%) 111 (88%) 11 (61%) 100 (93%) .001 
Median PFS 33 mo 17.2 mo 37.3 mo .001 
24-mo PFS 68% 32% 74% <.001 
36-mo PFS 49% 32% 52% <.001 
Median TTNT 40 mo 24.4 mo NR .001 
24-mo TTNT 75% 57% 79% .001 
36-mo TTNT 54% 34% 58% .001 
Impact of obinutuzumab RDI reduction >20% on outcome
CharacteristicOverall (n = 130)RDI reduction of obinutuzumab doseP value*
>20% (n = 20)≤20% (n = 110)
ORR, n (%) 111 (88%) 11 (61%) 100 (93%) .001 
Median PFS 33 mo 17.2 mo 37.3 mo .001 
24-mo PFS 68% 32% 74% <.001 
36-mo PFS 49% 32% 52% <.001 
Median TTNT 40 mo 24.4 mo NR .001 
24-mo TTNT 75% 57% 79% .001 
36-mo TTNT 54% 34% 58% .001 
Impact of patients’ characteristic on obinutuzumab RDI reduction > 20%
CharacteristicOverall (n = 130)RDI reduction of obinutuzumab dose
>20% (n = 20)≤20% (n = 110)P value*Q value
ECOG PS in class, n (%)    .027 .027 
 0-1 94 (72) 10 (50) 84 (76)   
 ≥2 36 (28) 10 (50) 26 (24)   
ANC before treatment, median (range) 3920 (313, 16 000) 3200 (313, 9290) 4100 (580, 16 000) .018 .29 
CIRS in class, n (%)    .085 .56 
 ≤6 49 (38) 4 (20) 45 (41)   
 >6 81 (62) 16 (80) 65 (59)   
Impact of patients’ characteristic on obinutuzumab RDI reduction > 20%
CharacteristicOverall (n = 130)RDI reduction of obinutuzumab dose
>20% (n = 20)≤20% (n = 110)P value*Q value
ECOG PS in class, n (%)    .027 .027 
 0-1 94 (72) 10 (50) 84 (76)   
 ≥2 36 (28) 10 (50) 26 (24)   
ANC before treatment, median (range) 3920 (313, 16 000) 3200 (313, 9290) 4100 (580, 16 000) .018 .29 
CIRS in class, n (%)    .085 .56 
 ≤6 49 (38) 4 (20) 45 (41)   
 >6 81 (62) 16 (80) 65 (59)   

ANC, absolute neutrophil count; NR, not reached.

*

Fisher's exact test.

False discovery rate correction for multiple testing.

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