Table 2.

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 
GPRC5D, n 
FcRH5, n 
BCMA + GPRC5D, n 
NK, n 
IMiDs-based schemes, n (%) 1 (5.3) 7 (33.3) 
PCd 
PVd 
Celmod 
PIs-based schemes, n (%) 1 (5.3) 4 (19.0) 
VCd, n 
SVd, n 
BendaVd, n 
Kd, n 
KCd, n 
Anti-CD38 moAb-based schemes, n (%) 1 (5.3) 1 (4.8) 
Daratumumab, n 
DRd, n 
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 
GPRC5D, n 
FcRH5, n 
BCMA + GPRC5D, n 
NK, n 
IMiDs-based schemes, n (%) 1 (5.3) 7 (33.3) 
PCd 
PVd 
Celmod 
PIs-based schemes, n (%) 1 (5.3) 4 (19.0) 
VCd, n 
SVd, n 
BendaVd, n 
Kd, n 
KCd, n 
Anti-CD38 moAb-based schemes, n (%) 1 (5.3) 1 (4.8) 
Daratumumab, n 
DRd, n 
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.

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