Table 1.
Characteristics | Patients (n = 12) |
---|---|
Median age (range), y | 63 (34-81) |
Male:female | 7:5 |
Infused/enrolled | 12/13 |
ECOG performance status, no. % | |
0-1 | 7/12 |
2+ | 5/12 |
Disease location | |
Parenchymal | 11/12 |
Leptomeningeal enhancement/CSF+ | 2/12 |
Cell of origin | |
Germinal center B-cell type | 1/12 |
Nongerminal center B-cell type | 11/12 |
Median no. of previous lines of antineoplastic therapy (range) | 4 (2-9) |
Prior methotrexate-based regimen | |
Yes | 12/12 |
No | 0/12 |
Prior thiotepa-based ASCT | |
Yes | 3/12 |
No | 9/12 |
BTKi refractory | |
Yes | 12/12 |
No | 0/12 |
IMiD refractory * | |
Yes | 4/12 |
No | 8/12 |
TEDDI-R refractory | |
Yes | 6/12 |
No | 6/12 |
Prior radiotherapy | |
Yes | 4/12 |
No | 8/12 |
Bridging therapy (including high-dose steroids) | |
Yes | 12/12 |
No | 0/12 |
Median vein-to-vein time, d | 33 (27-37) |
ECOG, Eastern cooperate oncology group performance status; TEDDI-R, temozolomide, etoposide, Doxil, dexamethasone, ibrutinib, and rituximab.
4 patients received IMiD as part of venetoclax, ibrutinib, prednisone, obinutuzumab, and lenalidomide.