Table 2.

Response rates after induction*

VRDVTD
GEM2012GEM2005
All patients, n (%)High-risk cytogenetics, n (%)All patients, n (%)High-risk cytogenetics, n (%)
(N = 458)(n = 92)(N = 130)(n = 23)
PR or better 382 (83.4) 75 (81.5) 110 (84.6) 18 (78.3) 
 CR 153 (33.4) 32 (34.8) 46 (35.4) 8 (34.8) 
 VGPR 152 (33.2) 33 (35.9) 32 (24.6) 5 (21.7) 
 PR 77 (16.8) 10 (10.9) 32 (24.6) 5 (21.7) 
VGPR or better 305 (66.6) 65 (70.7) 78 (60.0) 13 (56.5) 
Stable disease 20 (4.4) 7 (5.4) 2 (8.7) 
Progressive disease 31 (6.8) 14 (15.2) 9 (6.9) 1 (4.3) 
Not evaluable 25 (5.5) 3 (3.3)   
VRDVTD
GEM2012GEM2005
All patients, n (%)High-risk cytogenetics, n (%)All patients, n (%)High-risk cytogenetics, n (%)
(N = 458)(n = 92)(N = 130)(n = 23)
PR or better 382 (83.4) 75 (81.5) 110 (84.6) 18 (78.3) 
 CR 153 (33.4) 32 (34.8) 46 (35.4) 8 (34.8) 
 VGPR 152 (33.2) 33 (35.9) 32 (24.6) 5 (21.7) 
 PR 77 (16.8) 10 (10.9) 32 (24.6) 5 (21.7) 
VGPR or better 305 (66.6) 65 (70.7) 78 (60.0) 13 (56.5) 
Stable disease 20 (4.4) 7 (5.4) 2 (8.7) 
Progressive disease 31 (6.8) 14 (15.2) 9 (6.9) 1 (4.3) 
Not evaluable 25 (5.5) 3 (3.3)   

PR, partial response.

*

Efficacy data for GEM2012 was adjudicated by an independent response adjudication committee and IMWG criteria. The data for GEM2005 was based on investigator assessment with central review and European Society for Blood and Marrow Transplantation criteria with Uniform Response Criteria for VGPR categorization.

Data from Rosiñol at al.12 

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