Table 1

Baseline patient characteristics

CharacteristicN = 91
Male, n (%) 61 (67) 
Age  
 Median (range), years 58 (29-66) 
ISS stage, n (%)  
 1 38 (42) 
 2 31 (34) 
 3 22 (24) 
WHO performance status, n (%)  
 0 42 (46) 
 1 37 (41) 
 2 4 (4) 
 3 2 (2) 
 Unknown 6 (7) 
M-protein isotype, n (%)  
 IgA 20 (22) 
 IgG 48 (53) 
 IgD 3 (3) 
 Light-chain disease 17 (19) 
 Unknown 3 (3) 
M-protein light chain, n (%)  
 κ 59 (65) 
 Λ 29 (32) 
 Unknown 3 (3) 
Lytic bone lesions, n (%)  
 0 22 (24) 
 1 8 (9) 
 2 6 (7) 
 ≥3 53 (58) 
 Unknown 2 (2) 
Genetic abnormalities, n (%)*  
 add1q 11 (15) 
 t(4;14)(p16;q32) 4 (5) 
 del(17p13) 8 (11) 
Risk status, n (%)  
 Standard 36 (40) 
 High 35 (38) 
 Unknown 20 (22) 
Grade 1/2 PNP 7 (9) 
 Median β2-microglobulin (range), mg/L 3.6 (1.4-23.6) 
 Median hemoglobin (range), mmol/L 7.0 (4.3-10.4) 
 Median calcium (range), mmol/L 2.3 (2.0-4.1) 
 Median creatinine (range), µmol/L 79 (40-345) 
 Median creatinine clearance (range), mL/min§ 60 (26-118) 
CharacteristicN = 91
Male, n (%) 61 (67) 
Age  
 Median (range), years 58 (29-66) 
ISS stage, n (%)  
 1 38 (42) 
 2 31 (34) 
 3 22 (24) 
WHO performance status, n (%)  
 0 42 (46) 
 1 37 (41) 
 2 4 (4) 
 3 2 (2) 
 Unknown 6 (7) 
M-protein isotype, n (%)  
 IgA 20 (22) 
 IgG 48 (53) 
 IgD 3 (3) 
 Light-chain disease 17 (19) 
 Unknown 3 (3) 
M-protein light chain, n (%)  
 κ 59 (65) 
 Λ 29 (32) 
 Unknown 3 (3) 
Lytic bone lesions, n (%)  
 0 22 (24) 
 1 8 (9) 
 2 6 (7) 
 ≥3 53 (58) 
 Unknown 2 (2) 
Genetic abnormalities, n (%)*  
 add1q 11 (15) 
 t(4;14)(p16;q32) 4 (5) 
 del(17p13) 8 (11) 
Risk status, n (%)  
 Standard 36 (40) 
 High 35 (38) 
 Unknown 20 (22) 
Grade 1/2 PNP 7 (9) 
 Median β2-microglobulin (range), mg/L 3.6 (1.4-23.6) 
 Median hemoglobin (range), mmol/L 7.0 (4.3-10.4) 
 Median calcium (range), mmol/L 2.3 (2.0-4.1) 
 Median creatinine (range), µmol/L 79 (40-345) 
 Median creatinine clearance (range), mL/min§ 60 (26-118) 

Ig, immunoglobulin; PNP, polyneuropathy.

*

A total of 74 patients were evaluable for cytogenetics.

High-risk patients had ISS stage 3 disease and/or del17p and/or t(4;14) and/or add1q cytogenetic abnormalities. The remaining patients with available ISS status and cytogenetics were considered to have a standard risk.

Not recorded in 10 patients.

§

Evaluated from 36 patients.

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