Table 2

Data in high-risk cohorts for patients undergoing autologous transplant

TrialTime pointEFS all patientsEFS/PFS t(4;14)PFS del(17p)OS % all patientsOS % t(4;14)OS % del(17p)
VD vs VAD35,36  4 y 36 mo 28 mo 14 mo 77 63 49 
NR 16 mo NR 82 32 50 
VTD vs TD37  3 y 74% 69% NR 86 NR NR 
63% 37% NR 84 NR NR 
PAD vs VAD39  3 y 28 mo 25 mo 26 mo 85 66 69 
35 mo 21 mo 12 mo 80 44 17 
RVD→RVD* 3 y 32 mo NR 28 mo 93% NR 94% 
TrialTime pointEFS all patientsEFS/PFS t(4;14)PFS del(17p)OS % all patientsOS % t(4;14)OS % del(17p)
VD vs VAD35,36  4 y 36 mo 28 mo 14 mo 77 63 49 
NR 16 mo NR 82 32 50 
VTD vs TD37  3 y 74% 69% NR 86 NR NR 
63% 37% NR 84 NR NR 
PAD vs VAD39  3 y 28 mo 25 mo 26 mo 85 66 69 
35 mo 21 mo 12 mo 80 44 17 
RVD→RVD* 3 y 32 mo NR 28 mo 93% NR 94% 

EFS, event-free survival; NR, not reported; PAD, bortezomib, doxorubicin, and dexamethasone.

*

Only high-risk patients were enrolled.

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