Table 1.

Baseline demographic and clinical characteristics of the patients

CharacteristicsPatients (n = 28)Patients, leukapheresis (n = 33)
Age, y   
 <60 21 (75) 25 (76) 
 ≥60 7 (25) 8 (24) 
Sex   
 Male 11 (39) 12 (36) 
 Female 17 (61) 21 (64) 
ECOG performance status score   
 0-1 15 (54) 20 (61) 
 2 13 (46) 13 (39) 
Disease stage at study entry   
 I/II 5 (18) 6 (18) 
 III/IV 23 (82) 27 (82) 
Diagnosis by central histologic review   
 DLBCL 16 (57) 19 (58) 
 TFL 3 (11) 4 (12) 
 FL 6 (21) 6 (18) 
 Other (MCL, CLL/SLL) 3 (11) 4 (12) 
IHC   
 CD20+ 28 (100) 33 (100) 
 CD19+ 22 (79) 27 (82) 
 CD19 4 (14) 4 (12) 
 Missing CD19 data 2 (7) 2 (6) 
Double or triple expressor: MYC plus BCL2 or BCL6 or both   
 Yes 10 (36) 13 (39) 
 No 4 (14) 6 (18) 
 Missing data 14 (50) 14 (43) 
 Ki-67 (≥70%) 18 (64) 21 (64) 
Extranodal organ involvement   
 Yes 17 (61) 20 (61) 
 No 11 (39) 13 (39) 
No. of previous lines of antineoplastic therapy   
 ≤2 6 (21) 7 (21) 
 3-5 15 (54) 18 (55) 
 ≥6 7 (25) 8 (24) 
Patient with chronic viral hepatitis B   
 Yes 3 (11) 4 (12) 
 No 25 (89) 29 (88) 
Refractory or relapse   
 Refractory 24 (86) 28 (85) 
  Primary refractory* 9 (32) 11 (33) 
  Refractory to second-line or later therapy 15 (54) 18 (55) 
 Relapse after second-line or later therapy 4 (14) 5 (15) 
 Refractory to ASCT 5 (18) 5 (15) 
 Relapse after previous CD19 CAR T-cell therapy 3 (11) 3 (9) 
Tumor burden   
 SPD ≥100 cm2 7 (25) 10 (30) 
 SPD <100 cm2 21 (75) 23 (70) 
Bulky/nonbulky disease   
 Lesion diameter ≥10 cm 5 (18) 7 (21) 
 Lesion diameter <10 cm 23 (82) 26 (79) 
CharacteristicsPatients (n = 28)Patients, leukapheresis (n = 33)
Age, y   
 <60 21 (75) 25 (76) 
 ≥60 7 (25) 8 (24) 
Sex   
 Male 11 (39) 12 (36) 
 Female 17 (61) 21 (64) 
ECOG performance status score   
 0-1 15 (54) 20 (61) 
 2 13 (46) 13 (39) 
Disease stage at study entry   
 I/II 5 (18) 6 (18) 
 III/IV 23 (82) 27 (82) 
Diagnosis by central histologic review   
 DLBCL 16 (57) 19 (58) 
 TFL 3 (11) 4 (12) 
 FL 6 (21) 6 (18) 
 Other (MCL, CLL/SLL) 3 (11) 4 (12) 
IHC   
 CD20+ 28 (100) 33 (100) 
 CD19+ 22 (79) 27 (82) 
 CD19 4 (14) 4 (12) 
 Missing CD19 data 2 (7) 2 (6) 
Double or triple expressor: MYC plus BCL2 or BCL6 or both   
 Yes 10 (36) 13 (39) 
 No 4 (14) 6 (18) 
 Missing data 14 (50) 14 (43) 
 Ki-67 (≥70%) 18 (64) 21 (64) 
Extranodal organ involvement   
 Yes 17 (61) 20 (61) 
 No 11 (39) 13 (39) 
No. of previous lines of antineoplastic therapy   
 ≤2 6 (21) 7 (21) 
 3-5 15 (54) 18 (55) 
 ≥6 7 (25) 8 (24) 
Patient with chronic viral hepatitis B   
 Yes 3 (11) 4 (12) 
 No 25 (89) 29 (88) 
Refractory or relapse   
 Refractory 24 (86) 28 (85) 
  Primary refractory* 9 (32) 11 (33) 
  Refractory to second-line or later therapy 15 (54) 18 (55) 
 Relapse after second-line or later therapy 4 (14) 5 (15) 
 Refractory to ASCT 5 (18) 5 (15) 
 Relapse after previous CD19 CAR T-cell therapy 3 (11) 3 (9) 
Tumor burden   
 SPD ≥100 cm2 7 (25) 10 (30) 
 SPD <100 cm2 21 (75) 23 (70) 
Bulky/nonbulky disease   
 Lesion diameter ≥10 cm 5 (18) 7 (21) 
 Lesion diameter <10 cm 23 (82) 26 (79) 

All data are n (%).

ASCT, allogeneic stem cell transplantation; DLBCL, diffuse large B-cell lymphoma; ECOG, Eastern Cooperative Oncology Group; FL, follicular lymphoma; IHC, immunohistochemistry; MCL, mantle cell lymphoma; SPD, sum of the products of the longest perpendicular diameters; TFL, transformed follicular lymphoma.

*

Defined as ≥1 of the following: no response to first-line therapy (primary refractory disease); subjects who did not tolerate first-line therapy chemotherapy were excluded. PD was the best response to first-line therapy, and stable disease was the best response after ≥4 cycles of first-line therapy (eg, 4 cycles of R-CHOP [rituximab, cyclophosphamide, adriamycin, vincristine, prednisone]) with stable disease for ≤6 months from the last treatment dose.

Defined as disease progression or relapse ≤12 months after ASCT (biopsy-proven recurrence required for relapsed subjects).

Defined as disease progression or relapse ≤6 months after previous CD19 CAR T-cell therapy (biopsy-proven recurrence required for relapsed subjects).

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