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. 2021 Dec 17;5(24):5525–5535. doi: 10.1182/bloodadvances.2021004512

Table 1.

Clinical characteristics of patients with newly diagnosed lymphomas in the prospective cohort with no known CNS disease

Variable All CSF NGS-MRD assay P
Positive Negative
Patients, n 22 8 14
Age, y, median (range) 63 (27-83) 53 (38-76) 67 (27-83) .34
Female, n (%) 7 (32) 1 (13) 6 (43) .19
Histology, n (%) .76
 DLBCL 10 (45) 3 (38) 7 (50)
 HGBCL* 7 (32) 4 (50) 3 (21)
 THRLBCL 1 (5) 1 (7)
 Plasmablastic lymphoma 1 (5) 1 (7)
 BL 3 (14) 1 (13) 2 (14)
CNS-IPI, n (%) .99
 Low 2 (11) 1 (14) 1 (8)
 Intermediate 8 (42) 3 (43) 5 (42)
 High 9 (47) 3 (43) 6 (50)
LDH, U/mL, median (range) 401 (144-1619) 480 (191-1619) 287 (144-1553) .27
MRI brain performed, n (%) 11 (50) 4 (50) 7 (50) .99
First-line chemotherapy, n (%) .99
 R-CHOP 8 (36) 3 (38) 5 (36)
 DA-EPOCH-R 12 (55) 4 (50) 8 (57)
 Other 2 (9) 1 (13) 1 (7)
CNS prophylaxis .99
 High-dose methotrexate 6 (27) 2 (25) 4 (29)
 IT only 14 (64) 5 (63) 9 (64)
 None (declined) 2 (9) 1 (13) 1 (7)
 IT injections, n, median (range) 4 (1-9) 3.5 (2-9) 4 (1-6) .47
CSF cell count per cubic millimeter
 WBC, median (range) 1 (0-3) 1 (0-3) 0 (0-3) .38
 RBC, median (range) 14 (0-331) 31 (0-299) 8 (0-331) .38

DA-EPOCH-R, dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab; IT, intrathecal; LDH, lactate dehydrogenase; MRI, magnetic resonance imaging; R-CHOP, rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone; THRLBCL, T-cell/histiocyte-rich large B-cell lymphoma.

*

With MYC and BCL2 and/or BCL6 rearrangements.

Calculated for DLBCL, HGBCL, THRLBCL, and plasmablastic lymphoma only.

One patient each for rituximab alone and R-CODOX-M/IVAC (rituximab plus cyclophosphamide, doxorubicin, vincristine, methotrexate/ifosfamide, etoposide, and high-dose cytarabine).