Table 1.

Clinical and biological characteristics at baseline

CharacteristicsValueValid data (n)
Total population, n (%) 214 (100)  
Diagnosis period, n (%)   
 Diagnosis 2000-2005 50 (23.4) 214 
 Diagnosis 2006-2010 60 (28)  
 Diagnosis 2011-2015 104 (48.6)  
Sex, n (%)  214 
 Male 137 (64)  
 Female 77 (36)  
Age, y   
 Median ± standard deviation 37.2 ± 4.3  
 Minimum-maximum 18.6-40.9  
MGUS history, n (%) 19 (9.2) 206 
Type of disease, n (%)  214 
 Symptomatic MM 189 (88.3)  
pPCL 9 (4.2)  
SMM 10 (4.7)  
Solitary plasmacytoma 4 (1.9)  
Randall disease 2 (0.9)  
Isotype, n (%)  213 
 Complete isotype 162 (76)  
  IgA 28 (17.3)  
  IgG 130 (80.2)  
  IgM 1 (0.06)  
  IgD 3 (1.9)  
 Light chain only 51 (24)  
Light chain type, n (%)  209 
 κ 138 (66)  
 λ 71 (34)  
Bone lesions, n (%) 149 (75) 200 
Medical imaging, n (%)*  190 
 Standard radiography 100 (52.6)  
 CT imaging 64 (33.7)  
 MRI 114 (60)  
 PET 27 (14.2)  
 None 4 (2.1)  
Glomerular filtration rate (MDRD, ml/min), n (%)  200 
 ≥60 166 (83)  
 <60 34 (17)  
Hypercalcemia, n (%)  195 
 >2.75 mmol/L 25 (12.8)  
  ≤2.75 mmol/L 170 (87.2)  
Proteinuria >1 g/L, n (%) 34 (22.7) 150 
Albuminemia, median ± SD, g/L 39.2 ± 8.2 187 
β2-Microglobulinemia, median ± SD, g/L 2.83 ± 14.5 179 
Cytopenia, n (%)   
 Anemia (Hb <10 g/dL) 71 (35.1) 202 
 Neutropenia (PNN <1.5 G/L) 9 (4.7) 193 
 Thrombopenia (platelets <100 G/L) 8 (4) 199 
ISS score, n (%)  189 
 1 99 (52.4)  
 2 52 (27.5)  
 3 38 (20.1)  
Cytogenetics, n (%)   
 High risk, including*34 (18) 189 
  t(4;14) 19 (12.2) 189 
  del17p 17 (12.1) 156 
 Others, including 65 (34.4) 141 
  t(11;14) 9 (25.7) 189 
  t(14;16) 1 (2.5) 35 
  +1q 17 (30.4) 39 
  del1p32 8 (17.4) 56 
CharacteristicsValueValid data (n)
Total population, n (%) 214 (100)  
Diagnosis period, n (%)   
 Diagnosis 2000-2005 50 (23.4) 214 
 Diagnosis 2006-2010 60 (28)  
 Diagnosis 2011-2015 104 (48.6)  
Sex, n (%)  214 
 Male 137 (64)  
 Female 77 (36)  
Age, y   
 Median ± standard deviation 37.2 ± 4.3  
 Minimum-maximum 18.6-40.9  
MGUS history, n (%) 19 (9.2) 206 
Type of disease, n (%)  214 
 Symptomatic MM 189 (88.3)  
pPCL 9 (4.2)  
SMM 10 (4.7)  
Solitary plasmacytoma 4 (1.9)  
Randall disease 2 (0.9)  
Isotype, n (%)  213 
 Complete isotype 162 (76)  
  IgA 28 (17.3)  
  IgG 130 (80.2)  
  IgM 1 (0.06)  
  IgD 3 (1.9)  
 Light chain only 51 (24)  
Light chain type, n (%)  209 
 κ 138 (66)  
 λ 71 (34)  
Bone lesions, n (%) 149 (75) 200 
Medical imaging, n (%)*  190 
 Standard radiography 100 (52.6)  
 CT imaging 64 (33.7)  
 MRI 114 (60)  
 PET 27 (14.2)  
 None 4 (2.1)  
Glomerular filtration rate (MDRD, ml/min), n (%)  200 
 ≥60 166 (83)  
 <60 34 (17)  
Hypercalcemia, n (%)  195 
 >2.75 mmol/L 25 (12.8)  
  ≤2.75 mmol/L 170 (87.2)  
Proteinuria >1 g/L, n (%) 34 (22.7) 150 
Albuminemia, median ± SD, g/L 39.2 ± 8.2 187 
β2-Microglobulinemia, median ± SD, g/L 2.83 ± 14.5 179 
Cytopenia, n (%)   
 Anemia (Hb <10 g/dL) 71 (35.1) 202 
 Neutropenia (PNN <1.5 G/L) 9 (4.7) 193 
 Thrombopenia (platelets <100 G/L) 8 (4) 199 
ISS score, n (%)  189 
 1 99 (52.4)  
 2 52 (27.5)  
 3 38 (20.1)  
Cytogenetics, n (%)   
 High risk, including*34 (18) 189 
  t(4;14) 19 (12.2) 189 
  del17p 17 (12.1) 156 
 Others, including 65 (34.4) 141 
  t(11;14) 9 (25.7) 189 
  t(14;16) 1 (2.5) 35 
  +1q 17 (30.4) 39 
  del1p32 8 (17.4) 56 

Number of patients is expressed in absolute value (n), whereas percentage (%) is calculated among valid data, after exclusion of ND and NA values. CT, computed tomography; Hb, hemoglobin; IgA, immunoglobulin A; MDRD, Modification of Diet in Renal Disease equation; MGUS, monoclonal gammopathy of unknown significance; MRI, magnetic resonance imaging; PET, positron emission tomography; PNN, polynuclear neutrophil; SD, standard deviation.

*

Two patients had t(4;14) and del17p. Failure of cytogenetic analysis was considered as nonvalid data.

Associated with high-risk cytogenetics in 5 patients.

Associated with high-risk cytogenetics in 2 patients; associated with +1q in 5 patients.

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