Table 1

Baseline patient characteristics

CharacteristicsLow-dose group
(n=4)
Medium-dose group
(n=13)
High-dose group
(n=14)
Total
(n=31)
Median age, years (range)60.5 (54–72)64.0 (52–74)59.5 (45–71)61.0 (45–74)
 ≥65, n (%)2 (50.0)6 (46.2)4 (28.6)12 (38.7)
Male sex, n (%)2 (50.0)7 (53.8)8 (57.1)17 (54.8)
ECOG-PS, n (%)
 03 (75.0)5 (38.5)11 (78.6)19 (61.3)
 11 (25.0)8 (61.5)3 (21.4)12 (38.7)
Staging based on the R-ISS, n (%)
 I0 (0.0)2 (15.4)2 (14.3)4 (12.9)
 II4 (100.0)9 (69.2)8 (57.1)21 (67.7)
 III0 (0.0)2 (15.4)3 (21.4)5 (16.2)
 UK0 (0.0)0 (0.0)1 (7.1)1 (3.2)
Double-hit or triple-hit MM, n (%)
 Double-hit2 (50.0)5 (38.5)6 (42.9)13 (41.9)
 Triple-hit0 (0.0)1 (7.7)1 (7.1)2 (6.5)
High lactate dehydrogenase0 (0.0)2 (15.4)1 (7.1)3 (9.7)
MM type, n (%)
 IgA-κ0 (0.0)1 (7.7)0 (0.0)1 (3.2)
 IgA-λ0 (0.0)2 (15.4)2 (14.3)4 (12.9)
 IgD-λ0 (0.0)0 (0.0)1 (7.1)1 (3.2)
 IgG-κ2 (50.0)2 (15.4)4 (28.6)8 (25.8)
 IgG-λ0 (0.0)5 (38.5)2 (14.3)7 (22.6)
 Light chain2 (50.0)3 (23.1)4 (28.6)9 (29.0)
  κ1 (25.0)2 (15.4)2 (14.3)5 (16.1)
  λ1 (25.0)1 (7.7)2 (14.3)4 (12.9)
 Non-secretory0 (0.0)0 (0.0)1 (7.1)1 (3.2)
Extramedullary MM, n (%)0 (0.0)1 (7.7)2 (14.3)3 (9.7)
% bone marrow BCMA+plasma cells, median (range)0.4912 (0.026–0.4092)0.44 (0.0044–0.916)0.6921 (0.0587–0.9913)0.4912 (0.0044–0.9913)
BCMA density, median (range)7637 (136–8003)1023 (61–2756)572.5 (203–4422)806 (61–8003)
Previous therapeutic regimens, median (range)7.0 (5–7)4.0 (2–13)*4.0 (3–12)4.0 (2–13)
 Immunomodulatory agents and proteasome inhibitors4 (100.0)13 (100.0)14 (100.0)31 (100.0)
 ASCT2 (50.0)1 (7.7)4 (28.6)7 (22.6)
 Anti-CD38 mAb0 (0.0)3 (23.1)4 (28.6)7 (22.6)
Received bridging therapy, n (%)0 (0.0)3 (23.1)4 (28.6)7 (22.6)
  • *Two patients received two lines of anti-MM therapy.

  • ASCT, autologous stem cell transplantation; BCMA, B-cell maturation antigen; double-hit MM, two high-risk genetic abnormalities; ECOG-PS, Eastern Cooperative Oncology Group performance status; mAb, monoclonal antibody; MM, multiple myeloma; R-ISS, Revised International Staging System; triple-hit MM, three or more high-risk genetic abnormalities; UK, unknown.