Efficacy of bortezomib and thalidomide in DLI-refractory patients
Patient . | Stem cell source . | No. DLIs (maximum T-cell dose, T cells/kg) . | Interval DLI next therapy, mo . | Reason to add treatment . | Next therapy . | Response . | Response, mo . | Toxicity . |
---|---|---|---|---|---|---|---|---|
1 | Sibling | 2 (1 × 108) | 5 | NR to DLI | Bort 6 | PR | 6 | No |
2 | Sibling | 3 (1 × 108) | 4 | NR to DLI | Bort 8 | VGPR | 8+ | PNP grade 2 |
3 | Sibling | 2 (1 × 107) | 5 | NR to DLI | Bort 3 | PR | 3 | PNP grade 3; reason to stop therapy |
4 | MUD | 2 (1 × 107) | 5 | NR to DLI | Bort 8 | VGPR | 9 | PNP grade 2 |
5 | Sibling | 1 (1 × 107) | 4 | NR to DLI | Thal 100 | PR | 9+ | GVHD grade 1; death from lung embolus |
6 | Sibling | 1 (1 × 107) | 4 | NR to DLI | Thal 200 | PR | 6+ | GVHD grade 1 |
15 | Sibling | 1 (1 × 106) | 5 | NR to DLI | Bort 8 | PR | 9+ | PNP grade 2, dose reduction after cycle 3 |
28 | Sibling | 1 (1 × 107) | 15 | Relapse from CR | Thal 100 + bort 4 | CR | 19+ | No |
29 | Sibling | 1 (1 × 107) | 21 | Relapse from CR | Thal 100 + bort 4 | CR | 8+ | No |
32 | MUD | 1 (1.3 × 107) | 6 | NR to DLI | Thal 100 | PR | 8 | No |
35 | MUD | 2 (1 × 106) | 2 | NR to DLI | Thal 300 | PD | NA | No |
37 | Sibling | 1 (1 × 106) | 4 | NR to DLI | Thal 100-300 | PD | NA | No |
39 | Sibling | 2 (5 × 106) | 3 | NR to DLI | Thal 100-200 | PR | 7 | No |
39 | Sibling | 2 (5 × 106) | 10 | PD after thal | Bort 4 | CR | 6 | No |
41 | MUD | 1 (5 × 106) | 5 | NR to DLI | Thal 100 | PR | 24+ | No |
49 | Sibling | 1 (1 × 106) | 2 | NR to DLI | Thal 200 | PR | 14 | No |
54 | MUD | 1 (1 × 107) | 4 | NR to DLI | Bort 6 | PR | 6 | No |
59 | Sibling | 2 (1 × 108) | 1 | NR to DLI | Thal 100 | NR | NA | No |
59 | Sibling | 2 (1 × 108) | 3 | PD after thal | Bort 3 | PD | NA | PNP grade 2 |
63 | Sibling | 3 (1 × 108) | 14 | NR to DLI | Bort 8 | MR | 10 | No |
63 | Sibling | 3 (1 × 108) | 40 | PD after bort | Thal 100 | PR | 15+ | PNP grade 2 |
Patient . | Stem cell source . | No. DLIs (maximum T-cell dose, T cells/kg) . | Interval DLI next therapy, mo . | Reason to add treatment . | Next therapy . | Response . | Response, mo . | Toxicity . |
---|---|---|---|---|---|---|---|---|
1 | Sibling | 2 (1 × 108) | 5 | NR to DLI | Bort 6 | PR | 6 | No |
2 | Sibling | 3 (1 × 108) | 4 | NR to DLI | Bort 8 | VGPR | 8+ | PNP grade 2 |
3 | Sibling | 2 (1 × 107) | 5 | NR to DLI | Bort 3 | PR | 3 | PNP grade 3; reason to stop therapy |
4 | MUD | 2 (1 × 107) | 5 | NR to DLI | Bort 8 | VGPR | 9 | PNP grade 2 |
5 | Sibling | 1 (1 × 107) | 4 | NR to DLI | Thal 100 | PR | 9+ | GVHD grade 1; death from lung embolus |
6 | Sibling | 1 (1 × 107) | 4 | NR to DLI | Thal 200 | PR | 6+ | GVHD grade 1 |
15 | Sibling | 1 (1 × 106) | 5 | NR to DLI | Bort 8 | PR | 9+ | PNP grade 2, dose reduction after cycle 3 |
28 | Sibling | 1 (1 × 107) | 15 | Relapse from CR | Thal 100 + bort 4 | CR | 19+ | No |
29 | Sibling | 1 (1 × 107) | 21 | Relapse from CR | Thal 100 + bort 4 | CR | 8+ | No |
32 | MUD | 1 (1.3 × 107) | 6 | NR to DLI | Thal 100 | PR | 8 | No |
35 | MUD | 2 (1 × 106) | 2 | NR to DLI | Thal 300 | PD | NA | No |
37 | Sibling | 1 (1 × 106) | 4 | NR to DLI | Thal 100-300 | PD | NA | No |
39 | Sibling | 2 (5 × 106) | 3 | NR to DLI | Thal 100-200 | PR | 7 | No |
39 | Sibling | 2 (5 × 106) | 10 | PD after thal | Bort 4 | CR | 6 | No |
41 | MUD | 1 (5 × 106) | 5 | NR to DLI | Thal 100 | PR | 24+ | No |
49 | Sibling | 1 (1 × 106) | 2 | NR to DLI | Thal 200 | PR | 14 | No |
54 | MUD | 1 (1 × 107) | 4 | NR to DLI | Bort 6 | PR | 6 | No |
59 | Sibling | 2 (1 × 108) | 1 | NR to DLI | Thal 100 | NR | NA | No |
59 | Sibling | 2 (1 × 108) | 3 | PD after thal | Bort 3 | PD | NA | PNP grade 2 |
63 | Sibling | 3 (1 × 108) | 14 | NR to DLI | Bort 8 | MR | 10 | No |
63 | Sibling | 3 (1 × 108) | 40 | PD after bort | Thal 100 | PR | 15+ | PNP grade 2 |
Bort n indicates that patients received an intravenous bolus of bortezomib (1.3 mg/m2) on days 1, 4, 8, and 11 for n 3-week cycles; MUD, matched unrelated donor; Thal, thalidomide; PNP, polyneuropathy; GVHD, graft-versus-host disease; NR, no response; MR, minor response; PR, partial response; VGPR, very good partial response; CR, complete response; PD, progressive disease; NA, not applicable; and No, no WHO toxicity > 1.
Response to salvage therapy was assessed according to the criteria of the European Group for Blood and Marrow Transplantation (EBMT).3