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. 2018 Jun 25;97(11):2163–2171. doi: 10.1007/s00277-018-3401-y

Table 1.

Characteristics of patients

Characteristics All patients (N = 90) (%)
Age, years; median (range) 61 (29–84)
Sex (M/F) 48 (53)/42 (47)
Serum M-protein
 IgG 47 (52)
 IgA 22 (24)
 Light chain, kappa 7 (8)
 Light chain, lambda 11 (12)
 Others 3(3)
Durie-Salmon stage
 I/II/III 7 (8)/5 (5)/78 (87)
ISS stage
 I/II/III/NA 21 (23)/27 (30)/29 (32)/13 (14)
Cytogeneticsa
 Standard risk/high risk/NA 61 (68)/20 (22)/9 (10)
Myeloma bone disease on plain radiographs, yes/no 74 (82)/16 (18)
Time since diagnosis, years; median (range) 3.2 (0.5–9.5)
Previous number of therapiesb, median (range) 2 (1–7)
 ≤ 2 53 (59)
 > 2 37 (41)
Previous ASCT 49 (54)
Previous therapy before Len-dex
 Bortezomib-based regimens 36 (40)
 Both bortezomib- and thalidomide-based regimens 54 (60)
Laboratory data
 Serum M-proteinc, g/dL, median (range) 2.36 (1.02–6.06)
 Difference between serum iFLC and uninvolved FLC, median (range) 237.1 (5.2–34,151.9)
 Hb, g/dL, median (range) 11.0 (6.8–15.3)
 Ca, mg/dL, median (range) 9.0 (7.2–12.1)
 LDH, U/L, median (range) 395.5 (153–1078)

ASCT autologous stem cell transplantation, iFLC involved free light chain, Len-dex lenalidomide and low-dose dexamethasone, NA not available, LDH lactate dehydrogenase

aHigh-risk cytogenetics is defined as hypodiploid or deletion of chr13 on conventional cytogenetics or presence of t(4;14), t(14;16), and -17p on fluorescent in situ hybridization and/or conventional cytogenetics. All other cytogenetic abnormalities were considered standard risk

bInduction + ASCT was considered one therapeutic line

cPatients with measurable serum M protein of at least 1 g per 100 mL were included