Table 1

Patient demographics and disease characteristics of patients with MM

CharacteristicsNo. of patients (%)P value
Non-ASCTASCTTotal
Median age [range], years58 [26, 81]50 [32, 67]57 [26, 81]< 0.001
Age group at diagnosis, years< 0.001
 ≤ 65275 (82.1)115 (96.6)390 (85.9)
 > 6560 (17.9)4 (3.4)64 (14.1)
Gender0.302
 Female142 (42.4)44 (37.0)186 (41.0)
 Male193 (57.6)75 (63.0)268 (59.0)
M-component0.155
 IgG155 (46.3)54 (45.4)209 (46.0)
 IgA76 (22.7)21 (17.6)97 (21.4)
 IgD18 (5.4)14 (11.8)32 (7.0)
 Light chain76 (22.7)25 (21.0)101 (22.2)
 Other10 (3.0)5 (4.2)15 (3.3)
LDH0.118
 Normal273 (81.5)89 (74.8)362 (79.7)
 Elevated62 (18.5)30 (25.2)92 (20.3)
ISS stage0.009
 I63 (19.1)36 (31.0)99 (22.2)
 II120 (36.4)44 (37.9)164 (36.8)
 III147 (44.5)36 (31.0)183 (41.0)
R-ISS stage< 0.001
 I7 (3.5)14 (16.9)21 (7.4)
 II156 (77.2)56 (67.5)212 (74.4)
 III39 (19.3)13 (15.7)52 (18.2)
Extra-medullary disease0.780
 Yes63 (18.8)21 (17.6)84 (18.5)
 No272 (81.2)98 (82.4)370 (81.5)
Induction regimen
 PI-based203 (60.6)88 (73.9)291 (64.1)0.050
 IMiD-based52 (15.5)10 (8.4)62 (13.7)
 PI+IMiD-based19 (5.7)13 (10.9)32 (7.0)
 Conventional61 (18.2)8 (6.7)69 (15.2)
lq21+0.759
 Positive66 (51.6)29 (49.2)95 (50.8)
 Negative62 (48.4)30 (50.8)92 (49.2)
Del(17p13)0.496
 Positive12 (9.4)4 (6.5)16 (8.4)
 Negative116 (90.6)58 (93.5)174 (91.6)
Del(13q14)0.246
 Positive64 (50.0)25 (41.0)89 (47.1)
 Negative64 (50.0)36 (59.0)100 (52.9)
t(4;14)0.056
 Positive26 (35.1)7 (17.9)33 (29.2)
 Negative48 (64.9)32 (82.1)80 (70.8)
t(11;14)0.141
 Positive20 (27.4)16 (41.0)36 (32.1)
 Negative53 (72.6)23 (59.0)76 (67.9)
t(14;16)0.645
 Positive4 (5.5)3 (7.7)7 (6.2)
 Negative69 (94.5)36 (92.3)105 (93.8)
Cytogenetics0.415
 High risk36 (30.0)14 (24.1)50 (28.1)
 Standard risk84 (70.0)44 (75.9)128 (71.9)

ASCT, autologous stem cell transplantation; IgH, immunoglobulin heavy chain; IMiD, immunomodulatory drug; LDH, lactate dehydrogenase; MM, multiple myeloma; PI, proteasome inhibitor; ISS, International Staging System; R-ISS, Revised-International Staging System. High-risk cytogenetics was defined by the presence of t(4;14), t(14;16), or del(17p13). Standard risk cytogenetics was defined as the absence of these abnormalities.