Table 1.
Isa (N = 21) | |
---|---|
Age, median (range), yrs | 58 (46–72) |
< 65 years, n (%) | 18 (85.7) |
65 to < 75 years, n (%) | 3 (14.3) |
Female, n (%) | 11 (52.4) |
Male, n (%) | 10 (47.6) |
ECOG PS, n (%) | |
0 | 6 (28.6) |
1 | 12 (57.1) |
2 | 3 (14.3) |
Median time from initial diagnosis (range), yrs | 2.61 (0.7–10.9) |
ISS stage at study entry, n (%) | |
Stage I | 4 (19.0) |
Stage II | 7 (33.3) |
Stage III | 9 (42.9) |
Not known | 1 (4.8) |
Median BMPC (range) at study entry, % | 24.0 (0–97.0) |
Patients with bone lesions at study entry, n (%) | 16 (76.2) |
Number of prior lines, median (range) | 4 (2–11) |
Number of prior lines, n (%) | |
1 | 0 |
2 | 7 (33.3) |
3 | 2 (9.5) |
≥ 4 | 12 (57.1) |
Refractory to, n (%) | |
IMiD | 19 (90.5) |
PI | 14 (66.7) |
IMiD and PI | 12 (57.1) |
Refractory to last treatment regimen, n (%) | 20 (95.2) |
BMPC, bone marrow plasma cells; ECOG PS, Eastern Cooperative Oncology Group performance status; IMiD, immunomodulatory drug; Isa, isatuximab; ISS, international staging system; PI, proteasome inhibitor.