Table 1.

Patient demographic and baseline disease characteristics in the safety run-in population of GRIFFIN

D-RVd (N = 16)
Age, median (range), y 62.5 (46-65) 
 Category  
  <65 14 (87.5) 
  ≥65 2 (12.5) 
Sex  
 Male 8 (50.0) 
 Female 8 (50.0) 
Race  
 White 11 (68.8) 
 Black or African American 4 (25.0) 
 Asian 1 (6.3) 
ECOG performance status*  
 0 3 (18.8) 
 1 10 (62.5) 
 2 3 (18.8) 
ISS disease stage  
 I 12 (75.0) 
 II 2 (12.5) 
 III 2 (12.5) 
Cytogenetic risk profile  
 Standard 12 (75.0) 
 High risk 4 (25.0) 
Time since diagnosis of multiple myeloma, median (range), mo 1.6 (0-5) 
D-RVd (N = 16)
Age, median (range), y 62.5 (46-65) 
 Category  
  <65 14 (87.5) 
  ≥65 2 (12.5) 
Sex  
 Male 8 (50.0) 
 Female 8 (50.0) 
Race  
 White 11 (68.8) 
 Black or African American 4 (25.0) 
 Asian 1 (6.3) 
ECOG performance status*  
 0 3 (18.8) 
 1 10 (62.5) 
 2 3 (18.8) 
ISS disease stage  
 I 12 (75.0) 
 II 2 (12.5) 
 III 2 (12.5) 
Cytogenetic risk profile  
 Standard 12 (75.0) 
 High risk 4 (25.0) 
Time since diagnosis of multiple myeloma, median (range), mo 1.6 (0-5) 

Data are number of patients (% of total group), unless otherwise specified.

ECOG, Eastern Cooperative Oncology Group; ISS, International Staging System.

*

ECOG performance status is scored on a scale from 0 to 5, with 0 indicating no symptoms and higher scores indicating increasing disability.

The ISS disease stage is based on the combination of serum β2-microglobulin and albumin levels. Higher stages indicate more advanced disease.

Cytogenetic risk was assessed by fluorescence in situ hybridization (local testing); high risk was defined as the presence of del17p, t(4;14), or t(14;16) in patients with available cytogenetic risk data.

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