Baseline demographics
. | N (%) . |
---|---|
Age, median (range), y | 64 (40-80) |
Sex (male/female) | 35/13 (73%/27%) |
Race | |
White | 40 (83%) |
Asian | 4 (8.3%) |
Black or African-American | 2 (4.2%) |
Other | 2 (4.2%) |
Prior lines of therapy | |
Median (range) | 3 (1-9) |
1 | 19 (40%) |
2 | 4 (8.3%) |
3 | 8 (16.7%) |
≥4 | 17 (35%) |
ISS | |
I | 3 (6%) |
II | 6 (12%) |
III | 24 (50%) |
Previous therapy | |
Auto-SCT | 23 (48%) |
Immunomodulatory drug | 48 (100%) |
Lenalidomide | 48 (100%) |
Pomalidomide | 16 (33%) |
Proteasome inhibitor | 48 (100%) |
Bortezomib | 46 (96%) |
Carfilzomib | 14 (29%) |
Ixazomib | 3 (6%) |
CD38 monoclonal antibody∗ | 14 (29%) |
Daratumumab | 12 (25%) |
Isatuximab | 2 (4%) |
Penta-drug exposed† | 6 (13%) |
FISH | |
Standard risk | 21 (44%) |
High risk | 12 (25%) |
Del17p | 8 (17%) |
t(4;14) | 3 (6%) |
t(14;16) | 2 (4%) |
1q gain‡ | 14 (29%) |
Unknown | 15 (31%) |
. | N (%) . |
---|---|
Age, median (range), y | 64 (40-80) |
Sex (male/female) | 35/13 (73%/27%) |
Race | |
White | 40 (83%) |
Asian | 4 (8.3%) |
Black or African-American | 2 (4.2%) |
Other | 2 (4.2%) |
Prior lines of therapy | |
Median (range) | 3 (1-9) |
1 | 19 (40%) |
2 | 4 (8.3%) |
3 | 8 (16.7%) |
≥4 | 17 (35%) |
ISS | |
I | 3 (6%) |
II | 6 (12%) |
III | 24 (50%) |
Previous therapy | |
Auto-SCT | 23 (48%) |
Immunomodulatory drug | 48 (100%) |
Lenalidomide | 48 (100%) |
Pomalidomide | 16 (33%) |
Proteasome inhibitor | 48 (100%) |
Bortezomib | 46 (96%) |
Carfilzomib | 14 (29%) |
Ixazomib | 3 (6%) |
CD38 monoclonal antibody∗ | 14 (29%) |
Daratumumab | 12 (25%) |
Isatuximab | 2 (4%) |
Penta-drug exposed† | 6 (13%) |
FISH | |
Standard risk | 21 (44%) |
High risk | 12 (25%) |
Del17p | 8 (17%) |
t(4;14) | 3 (6%) |
t(14;16) | 2 (4%) |
1q gain‡ | 14 (29%) |
Unknown | 15 (31%) |
Data are presented for 48 patients.
FISH, fluorescence in situ hybridization; ISS, International Staging System; Auto-SCT, autologous stem cell transplantation.
Hundred percent were refractory to anti-CD38 antibody (and also triple-class exposed based on the eligibility criteria for the trial); 7 patients had anti-CD38 antibody as the last line of therapy.
Penta drug included lenalidomide, bortezomib, carfilzomib, pomalidomide, and anti-CD38 antibody.
No patients had 1q amplification (defined as ≥4 copies).