Table 2.

Characteristics and response rate of first and subsequent salvage treatments

Treatment groupFirst line of salvage treatmentAll lines of salvage treatment
N% usedN ≥ PR
ORR
N ≥ VGPR
%
N% usedN ≥ PR
ORR
N ≥ VGPR
%
Allo-SCT 0.0% 0/0
N/A 
0/0
N/A 
3.0% 4/4
100.0% 
2/4
50.0% 
Auto-SCT 3.8% 1/3
33.3% 
1/3
33.3% 
14 5.9% 10/14
71.4% 
7/14<
50.0% 
BCMA ADC 1.3% 0/1
0.0% 
0/1
0.0% 
3.8% 2/8
25.0% 
2/8
25.0% 
Bispecific trial 11 13.9% 7/10
70.0% 
5/10
50.0% 
32 13.5% 17/29
58.6% 
12/29
41.4% 
BCMA-directed bispecific trial 2.5% 1 out of 2
50.0% 
0 out of 2
0.0% 
3.8% 4 out of 9
44.4% 
3 out of 9
33.3% 
Non-BCMA–directed bispecific trial 11.4% 6 out of 8
75.0% 
5 out of 8
62.5% 
23 9.7% 13 out of 20
65.0% 
9 out of 20
45.0% 
CAR T trial 2.5% 2 out of 2
100.0% 
1 out of 2
50.0% 
2.5% 5 out of 6
83.3% 
3 out of 6
50.0% 
Chemotherapy with or without stem cell support 20 25.3% 11 out of 19
57.9% 
4 out of 19
21.1% 
53 22.4% 29 out of 51
56.9% 
12 out of 51
23.5% 
Doublet/triplet/quadruplet combination of approved agents 23 29.1% 7 out of 22
31.8% 
2 out of 22
9.1% 
56 23.6% 15 out of 53
28.3% 
4 out of 53
7.5% 
Selinexor-based therapy 6.3% 2 out of 5
40.0% 
2 out of 5
40.0% 
15 6.3% 3 out of 14
21.4% 
3 out of 14
21.4% 
Venetoclax-based therapy 3.8% 2 out of 3
66.7% 
1 out of 3
33.3% 
14 5.9% 5 out of 14
35.7% 
2 out of 14
14.3% 
Other combinations (including MAPKi, checkpoint inhibitor or other trial) 11 13.9% 1 out of 11
9.1% 
0 out of 11
0.0% 
31 13.1% 12 out of 31
38.7% 
1 out of 31
3.2% 
All treatment groups 79 100.0% 33 out of 76
43.4% 
16 out of 76
21.1% 
237 100.0% 101 out of 224
45.1% 
48 out of 224
21.4% 
 Total N = 79 Total N = 76 Total N = 237 Total N = 224 
Treatment groupFirst line of salvage treatmentAll lines of salvage treatment
N% usedN ≥ PR
ORR
N ≥ VGPR
%
N% usedN ≥ PR
ORR
N ≥ VGPR
%
Allo-SCT 0.0% 0/0
N/A 
0/0
N/A 
3.0% 4/4
100.0% 
2/4
50.0% 
Auto-SCT 3.8% 1/3
33.3% 
1/3
33.3% 
14 5.9% 10/14
71.4% 
7/14<
50.0% 
BCMA ADC 1.3% 0/1
0.0% 
0/1
0.0% 
3.8% 2/8
25.0% 
2/8
25.0% 
Bispecific trial 11 13.9% 7/10
70.0% 
5/10
50.0% 
32 13.5% 17/29
58.6% 
12/29
41.4% 
BCMA-directed bispecific trial 2.5% 1 out of 2
50.0% 
0 out of 2
0.0% 
3.8% 4 out of 9
44.4% 
3 out of 9
33.3% 
Non-BCMA–directed bispecific trial 11.4% 6 out of 8
75.0% 
5 out of 8
62.5% 
23 9.7% 13 out of 20
65.0% 
9 out of 20
45.0% 
CAR T trial 2.5% 2 out of 2
100.0% 
1 out of 2
50.0% 
2.5% 5 out of 6
83.3% 
3 out of 6
50.0% 
Chemotherapy with or without stem cell support 20 25.3% 11 out of 19
57.9% 
4 out of 19
21.1% 
53 22.4% 29 out of 51
56.9% 
12 out of 51
23.5% 
Doublet/triplet/quadruplet combination of approved agents 23 29.1% 7 out of 22
31.8% 
2 out of 22
9.1% 
56 23.6% 15 out of 53
28.3% 
4 out of 53
7.5% 
Selinexor-based therapy 6.3% 2 out of 5
40.0% 
2 out of 5
40.0% 
15 6.3% 3 out of 14
21.4% 
3 out of 14
21.4% 
Venetoclax-based therapy 3.8% 2 out of 3
66.7% 
1 out of 3
33.3% 
14 5.9% 5 out of 14
35.7% 
2 out of 14
14.3% 
Other combinations (including MAPKi, checkpoint inhibitor or other trial) 11 13.9% 1 out of 11
9.1% 
0 out of 11
0.0% 
31 13.1% 12 out of 31
38.7% 
1 out of 31
3.2% 
All treatment groups 79 100.0% 33 out of 76
43.4% 
16 out of 76
21.1% 
237 100.0% 101 out of 224
45.1% 
48 out of 224
21.4% 
 Total N = 79 Total N = 76 Total N = 237 Total N = 224 

PR, partial response; VGPR, very good partial response.

or Create an Account

Close Modal
Close Modal