Salvage therapies used in TCR patients who relapsed from novel immunotherapy
. | CAR-T (n = 17) . | BiAbs (n = 21) . |
---|---|---|
BiAbs, n (%) | 9 (47.4) | 6 (28.6) |
BCMA, n | 0 | 0 |
GPRC5D, n | 6 | 3 |
FcRH5, n | 2 | 1 |
BCMA + GPRC5D, n | 1 | 1 |
NK, n | 0 | 1 |
IMiDs-based schemes, n (%) | 1 (5.3) | 7 (33.3) |
PCd | 0 | 5 |
PVd | 1 | 1 |
Celmod | 0 | 1 |
PIs-based schemes, n (%) | 1 (5.3) | 4 (19.0) |
VCd, n | 0 | 1 |
SVd, n | 0 | 1 |
BendaVd, n | 0 | 1 |
Kd, n | 0 | 1 |
KCd, n | 1 | 0 |
Anti-CD38 moAb-based schemes, n (%) | 1 (5.3) | 1 (4.8) |
Daratumumab, n | 0 | 1 |
DRd, n | 1 | 0 |
Allo-SCT, n (%) | 1 (5.3) | 0 (0.0) |
BCMA CAR-Ts, n (%) | 1 (5.3) | 1 (4.8) |
Venetoclax, n (%) | 1 (5.3) | 1 (4.8) |
Polychemotherapy, n (%) | 2 (10.5) | 1 (4.8) |
. | CAR-T (n = 17) . | BiAbs (n = 21) . |
---|---|---|
BiAbs, n (%) | 9 (47.4) | 6 (28.6) |
BCMA, n | 0 | 0 |
GPRC5D, n | 6 | 3 |
FcRH5, n | 2 | 1 |
BCMA + GPRC5D, n | 1 | 1 |
NK, n | 0 | 1 |
IMiDs-based schemes, n (%) | 1 (5.3) | 7 (33.3) |
PCd | 0 | 5 |
PVd | 1 | 1 |
Celmod | 0 | 1 |
PIs-based schemes, n (%) | 1 (5.3) | 4 (19.0) |
VCd, n | 0 | 1 |
SVd, n | 0 | 1 |
BendaVd, n | 0 | 1 |
Kd, n | 0 | 1 |
KCd, n | 1 | 0 |
Anti-CD38 moAb-based schemes, n (%) | 1 (5.3) | 1 (4.8) |
Daratumumab, n | 0 | 1 |
DRd, n | 1 | 0 |
Allo-SCT, n (%) | 1 (5.3) | 0 (0.0) |
BCMA CAR-Ts, n (%) | 1 (5.3) | 1 (4.8) |
Venetoclax, n (%) | 1 (5.3) | 1 (4.8) |
Polychemotherapy, n (%) | 2 (10.5) | 1 (4.8) |
Allo-SCT, allogeneic stem cell transplantation; BCMA, B-cell maturation antigen; Benda, bendamustine; C, cyclophosphamide; Celmod, Cereblon E3 Ligase Modulatory Drugs; DRd, daratumumab lenalidomide dexamethasone; FcRH5, Fc receptor homolog 5; GPRC5D, G protein–coupled receptor class C group 5 member D; Kd, carfilzomib dexamethasone; KCd, carfilzomib cyclophosphamide dexamethasone; NK, natural killer lymphocyte; P, pomalidomide; SVd, Selinexor bortezomib dexamethasone; VCd, bortezomib cyclophosphamide dexamethasone.