Table 1.

Characteristics of patients in the present series and those treated in the L-MIND study for reference

CharacteristicReal worldL-MIND
Number of patients 178 81 
Female sex 87 (49) 37 (46) 
Age (y), median (range) 75 (26-94) 72 (41-86) 
Race   
White, all ethnicity 161 (90) 72 (89) 
Asian 9 (5) 2 (2) 
Other or unknown 8 (4) 1 (1) 
Diagnosis   
DLBCL-NOS 96 (54) 72 (89) 
Transformed indolent lymphoma 59 (33) 7 (9) 
HGBCL (nontransformed) 19 (11) 2 (2) 
Other  4 (2) 0 (0) 
Cell of origin by immunohistochemistry   
GCB 100 (56) 38 (47) 
Non-GCB 62 (35) 21 (26) 
Unknown 16 (9) 22 (27) 
Risk (IPI)   
0-2 43 (27) 40 (49) 
3-5 114 (73) 41 (51) 
Ann Arbor stage   
I-II 20 (12) 20 (25) 
III-IV 149 (88) 61 (75) 
Prior lines of therapy for DLBCL   
Median (range) 2 (0-11) 2 (1-4) 
0  12 (7) 0 (0) 
49 (28) 40 (49) 
49 (28) 35 (43) 
27 (15) 5 (6) 
13 (7) 1 (1) 
≥5 28 (16) 0 (0) 
Primary refractory (progression within 6 months of first-line therapy) 87 (49) 15 (18) 
Refractory to last therapy 118 (67) 36 (44) 
Prior SCT 23 (13) 9 (11) 
Prior CAR-T 52 (30) 
L-MIND eligible (not considering laboratory values) 33 (22) 
L-MIND eligible (including laboratory values) 16 (11) 
Disease features for L-MIND exclusion   
Primary refractory (progression within 3 months of first-line therapy) 63 (37) 
Prior CAR-T 52 (30) 
4 or more prior lines of therapy for DLBCL 41 (23) 
Prior lenalidomide or IMiD 22 (13) 
HGBCL with double or triple hit cytogenetic 28 (17) 
History of CNS disease 16 (9) 
ECOG PS > 2 21 (13) 
Other characteristics for L-MIND exclusion   
Liver function test or blood count abnormalities 53 (31) 
Inadequate renal function (EGFR < 60) 51 (30) 
Other malignancy within 5 y 29 (16) 
Hepatitis B 3 (2) 
Hepatitis C 2 (1) 
HIV 1 (1) 
CharacteristicReal worldL-MIND
Number of patients 178 81 
Female sex 87 (49) 37 (46) 
Age (y), median (range) 75 (26-94) 72 (41-86) 
Race   
White, all ethnicity 161 (90) 72 (89) 
Asian 9 (5) 2 (2) 
Other or unknown 8 (4) 1 (1) 
Diagnosis   
DLBCL-NOS 96 (54) 72 (89) 
Transformed indolent lymphoma 59 (33) 7 (9) 
HGBCL (nontransformed) 19 (11) 2 (2) 
Other  4 (2) 0 (0) 
Cell of origin by immunohistochemistry   
GCB 100 (56) 38 (47) 
Non-GCB 62 (35) 21 (26) 
Unknown 16 (9) 22 (27) 
Risk (IPI)   
0-2 43 (27) 40 (49) 
3-5 114 (73) 41 (51) 
Ann Arbor stage   
I-II 20 (12) 20 (25) 
III-IV 149 (88) 61 (75) 
Prior lines of therapy for DLBCL   
Median (range) 2 (0-11) 2 (1-4) 
0  12 (7) 0 (0) 
49 (28) 40 (49) 
49 (28) 35 (43) 
27 (15) 5 (6) 
13 (7) 1 (1) 
≥5 28 (16) 0 (0) 
Primary refractory (progression within 6 months of first-line therapy) 87 (49) 15 (18) 
Refractory to last therapy 118 (67) 36 (44) 
Prior SCT 23 (13) 9 (11) 
Prior CAR-T 52 (30) 
L-MIND eligible (not considering laboratory values) 33 (22) 
L-MIND eligible (including laboratory values) 16 (11) 
Disease features for L-MIND exclusion   
Primary refractory (progression within 3 months of first-line therapy) 63 (37) 
Prior CAR-T 52 (30) 
4 or more prior lines of therapy for DLBCL 41 (23) 
Prior lenalidomide or IMiD 22 (13) 
HGBCL with double or triple hit cytogenetic 28 (17) 
History of CNS disease 16 (9) 
ECOG PS > 2 21 (13) 
Other characteristics for L-MIND exclusion   
Liver function test or blood count abnormalities 53 (31) 
Inadequate renal function (EGFR < 60) 51 (30) 
Other malignancy within 5 y 29 (16) 
Hepatitis B 3 (2) 
Hepatitis C 2 (1) 
HIV 1 (1) 

Values are represented as number (%) unless otherwise stated.

CNS, central nervous system; EGFR, estimated glomerular filtration rate; GCB, germinal center B-cell; HGBCL, high-grade B cell lymphoma; IMiD, immunomodulatory drug; IPI, international prognostic index; NOS, not otherwise specified; SCT, stem cell transplantation.

Other diagnoses: T-cell histiocyte-rich B-cell lymphoma (2), primary mediastinal B-cell lymphoma (2), posttransplant lymphoproliferative disorder with DLBCL morphology (1).

Twelve patients with transformed indolent lymphoma had received prior therapy for indolent disease but not for aggressive LBCL.

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