Table 1

Baseline characteristics

N = 44
Age, y, median (range) 63 (45-86) 
Male, n (%) 19 (43) 
ECOG PS, n (%)  
 0 4 (9) 
 1 23 (52) 
 2 17 (38) 
Cytogenetic/FISH markers, n (%)  
 Standard risk 23 (52) 
 High risk 20 (45) 
 Unknown 1 (2) 
Creatinine clearance, n (%)  
 <30 mL/min 7 (16) 
 30-60 mL/min 13 (30) 
 >60 mL/min 24 (55) 
Prior lines of therapy, median (range) 5 (1-11) 
Prior therapy, n (%)  
 Lenalidomide or thalidomide 44 (100) 
 Bortezomib 44 (100) 
 Autologous SCT 32 (72) 
 Allogeneic SCT 10 (22) 
 Alkylating agent 42 (95) 
 Dexamethasone 44 (100) 
 Anthracycline 26 (59) 
 VDT-PACE or DCEP 18 (41) 
Refractory to prior therapy, n (%)  
 Lenalidomide 34 (77) 
 Bortezomib 34 (77) 
 Bortezomib and lenalidomide 28 (64) 
N = 44
Age, y, median (range) 63 (45-86) 
Male, n (%) 19 (43) 
ECOG PS, n (%)  
 0 4 (9) 
 1 23 (52) 
 2 17 (38) 
Cytogenetic/FISH markers, n (%)  
 Standard risk 23 (52) 
 High risk 20 (45) 
 Unknown 1 (2) 
Creatinine clearance, n (%)  
 <30 mL/min 7 (16) 
 30-60 mL/min 13 (30) 
 >60 mL/min 24 (55) 
Prior lines of therapy, median (range) 5 (1-11) 
Prior therapy, n (%)  
 Lenalidomide or thalidomide 44 (100) 
 Bortezomib 44 (100) 
 Autologous SCT 32 (72) 
 Allogeneic SCT 10 (22) 
 Alkylating agent 42 (95) 
 Dexamethasone 44 (100) 
 Anthracycline 26 (59) 
 VDT-PACE or DCEP 18 (41) 
Refractory to prior therapy, n (%)  
 Lenalidomide 34 (77) 
 Bortezomib 34 (77) 
 Bortezomib and lenalidomide 28 (64) 

DCEP, dexamethasone, cyclophosphamide, etoposide, cisplatin; PS, performance status; VDT-PACE, bortezomib, dexamethasone, thalidomide, cisplatin, doxorubicin, cyclophosphamide, and etoposide.

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