Table 1

Characteristics of MM patients

NDMM (n=10)RRMM (n=10)DARA-R MM (n=9)
Age, years, median (range)61 (51–86)63 (54–77)65 (56–80)
Male, n (%)9 (90)6 (60)6 (67)
LDH, U/L
 Median (range)203 (133–334)185 (58–1505)200 (81–294)
 Unknown, n (%)3 (30)00
 Elevated, n (%)1 (14)1 (10)2 (22)
eGFR, mL/min/1.73 m2
 Median (range)88 (12–90)86 (39–90)82 (45–90)
 Unknown, n (%)1 (10)00
B2-microglobulin, mg/L
 Median (range)3,8 (2,1–12)NANA
 Unknown, n (%)3 (30)
M protein, n (%)
 IgG3 (33)6 (60)3 (33)
 IgA2 (22)2 (20)5 (56)
 FLC only4 (44)2 (20)1 (11)
 Non-secretor000
 Unknown1 (10)00
ISS score at diagnosis, n (%)
 13 (33)NANA
 23 (33)
 33 (33)
 Unknown1 (10)
High risk cytogenetics,* n (%)2 (22)1 (11)6 (67)
 del(17 p)203
 t(4;14)113
 t(14;16)000
 Unknown110
Prior lines, median (range)03 (2–5)4 (1–6)
Prior autologous SCT, n (%)NA7 (70)8 (89)
 Single4 (40)6 (67)
 Double3 (30)2 (22)
Prior allogeneic SCT, n (%)NA01 (11)
Thalidomide, n (%)NA
 Exposed4 (40)2 (22)
 Refractory†00
Lenalidomide, n (%)NA
 Exposed9 (90)8 (89)
 Refractory8 (80)7 (78)
Pomalidomide, n (%)NA
 Exposed4 (40)0
 Refractory4 (40)0
Bortezomib, n (%)NA
 Exposed9 (90)9 (100)
 Refractory2 (20)0
Carfilzomib, n (%)NA
 Exposed3 (30)2 (22)
 Refractory2 (20)1 (11)
Ixazomib, n (%)NA
 Exposed1 (10)2 (22)
 Refractory1 (10)2 (22)
Daratumumab, n (%)NA
 Exposed09 (100)
 Refractory09
Nivolumab, n (%)NA
 Exposed05 (56)
 Refractory05 (56)
IMiD,‡ n (%)NA
 Exposed10 (100)9 (100)
 Refractory10 (100)7 (78)
PI,§ n (%)NA
 Exposed10 (100)9 (100)
 Refractory5 (50)3 (33)
IMID and PI, n (%)NA
 Exposed10 (100)9 (100)
 Refractory5 (50)3 (33)
Triple class,¶ n (%)NA
 Exposed09 (100)
 Refractory03 (33)
Radiotherapy, n (%)
 No8 (89)5 (50)7 (78)
 Yes1 (11)5 (50)2 (22)
 Unknown1 (10)00
Extramedullary plasmacytomas, n (%)
 No9 (100)8 (80)9 (100)
 Yes02 (20)0
 Unknown1 (10)00
  • *Based on the presence of del(17 p), t(4;14) and/or t(14;16).

  • †Refractory disease was defined as progressive disease during therapy, no response (less than partial response), or progressive disease within 60 days of stopping treatment, according to the International Uniform Response Criteria for MM. BM samples were obtained at the time of diagnosis for newly diagnosed patients, and at the time of progression for other patients (n=19). Of these 19 patients, 8 progressed during their last line of therapy, and 7 patients progressed within 60 days after treatment was stopped. Four samples were collected at progression >60 days after stopping the last line of treatment.

  • ‡Thalidomide, lenalidomide and/or pomalidomide.

  • §Bortezomib, carfilzomib, and/or ixazomib.

  • ¶At least 1 IMiD, 1 PI, and CD38-targeting antibody.

  • BM, bone marrow; DRMM, daratumumab refractory MM; eGFR, estimated glomerular filtration rate; FLC, free light chains; IMiD, immunomodulatory drug; ISS, International Staging System; LDH, lactate dehydrogenase; MM, multiple myeloma; NA, not applicable; NDMM, newly diagnosed MM; PI, proteasome inhibitor ; RRMM, relapsed/refractory MM; SCT, stem cell transplantation.