Table 1.

Baseline characteristics of 38 patients who progressed and 18 patients without disease progression after CAR T-cell therapy

CharacteristicRelapse after CAR T-cells, n = 38No relapse after CAR T-cells, n = 18P
Median age at CD19 CAR T-cell therapy (range), y 42.5 (23-74) 55 (23-68) .21 
Male sex 28 (73.7%) 14 (77.8%) 1.00 
Median lines of treatment before CAR T-cell therapy (range) 3 (2-7) 2 (1-7) .02 
Philadelphia chromosome–positive ALL (%) p190 p210 13 (34.2) 8 (21.1) 5 (13.1) 4 (22.2) 3 (16.7) 1 (5.6) .74 
Prior treatment with noncellular immunotherapy*(%) Blinatumomab Inotuzumab ozogamicin  10 (26.3) 3 (7.9)  3 (16.7) 1 (5.6) 1.00 
Prior HSCT before CAR T-cell therapy (%) 17 (44.7) 3 (16.7) .11 
Bridging therapy(%) Intensive therapy Nonintensive therapy None  10 (26.3) 21 (55.3) 7 (18.4)  10 (55.6) 7 (38.9) 1 (5.6) .12 
Disease burden before CAR T-cell therapy (%) Morphologic disease MRD No evidence of disease  26 (68.4) 11 (28.9) 1 (2.6)  5 (27.8) 6 (33.3) 6 (33.3) .01 
CRS post-CAR T-cell therapy (%) Grade 3 or higher CRS 32 (84.2) 9 (23.7) 16 (88.9) 6 (33.3) .52 
ICANS (%) Grade 3 or higher ICANS 22 (57.9) 14 (36.8) 12 (66.7) 10 (55.6) .19 
Tocilizumab for CRS/ICANS management (%) 15 (39.5) 5 (27.8) .39 
Systemic corticosteroid for CRS/ICANS management (%) 12 (31.6) 7 (38.9) .59 
Median time from CAR T-cell infusion to corticosteroid (range, d) 7 (5-15) 8 (3-12) .80 
Median duration of systemic corticosteroid (range, d) 7 (1-15) 9 (2-27) .16 
Median dose intensity of steroid (prednisone equivalent, mg/kg/d) 1.37 (0.72-2.58) 1.54 (0.79-6.75) .38 
HSCT consolidation after CAR T-cell therapy (%) 6 (15.8) 9 (50.0) .10 
CharacteristicRelapse after CAR T-cells, n = 38No relapse after CAR T-cells, n = 18P
Median age at CD19 CAR T-cell therapy (range), y 42.5 (23-74) 55 (23-68) .21 
Male sex 28 (73.7%) 14 (77.8%) 1.00 
Median lines of treatment before CAR T-cell therapy (range) 3 (2-7) 2 (1-7) .02 
Philadelphia chromosome–positive ALL (%) p190 p210 13 (34.2) 8 (21.1) 5 (13.1) 4 (22.2) 3 (16.7) 1 (5.6) .74 
Prior treatment with noncellular immunotherapy*(%) Blinatumomab Inotuzumab ozogamicin  10 (26.3) 3 (7.9)  3 (16.7) 1 (5.6) 1.00 
Prior HSCT before CAR T-cell therapy (%) 17 (44.7) 3 (16.7) .11 
Bridging therapy(%) Intensive therapy Nonintensive therapy None  10 (26.3) 21 (55.3) 7 (18.4)  10 (55.6) 7 (38.9) 1 (5.6) .12 
Disease burden before CAR T-cell therapy (%) Morphologic disease MRD No evidence of disease  26 (68.4) 11 (28.9) 1 (2.6)  5 (27.8) 6 (33.3) 6 (33.3) .01 
CRS post-CAR T-cell therapy (%) Grade 3 or higher CRS 32 (84.2) 9 (23.7) 16 (88.9) 6 (33.3) .52 
ICANS (%) Grade 3 or higher ICANS 22 (57.9) 14 (36.8) 12 (66.7) 10 (55.6) .19 
Tocilizumab for CRS/ICANS management (%) 15 (39.5) 5 (27.8) .39 
Systemic corticosteroid for CRS/ICANS management (%) 12 (31.6) 7 (38.9) .59 
Median time from CAR T-cell infusion to corticosteroid (range, d) 7 (5-15) 8 (3-12) .80 
Median duration of systemic corticosteroid (range, d) 7 (1-15) 9 (2-27) .16 
Median dose intensity of steroid (prednisone equivalent, mg/kg/d) 1.37 (0.72-2.58) 1.54 (0.79-6.75) .38 
HSCT consolidation after CAR T-cell therapy (%) 6 (15.8) 9 (50.0) .10 
*

One patient received both blinatumomab and inotuzumab ozogamicin before CD19 CAR T-cell therapy.

Intensive therapy included multiagent, myelosuppressive, chemotherapy-based regimen, and nonintensive regimen included nonmyelosuppressive chemotherapy or antibody-based therapy (eg, blinatumomab, inotuzumab). Breakdown of bridging intensity according to disease burden is provided in supplemental Figure 1.

Per American Society of Transplant and Cellular Therapy criteria.

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