Cohort1: dose level 1
|
Administration route |
None |
Dosage |
3E5 cells/kg |
Donor type |
Autologous|Allogeneic |
Pts |
3 |
Age |
Child, Adult |
Lymph depletion |
Yes |
Outcome |
0/3(CR).No Dose-limiting toxicities |
Adverse reactions |
0/3(≥Grade 3 CRS) |
References |
DOI:
10.1182/blood-2023-179667
|
|
Cohort2: dose level 2
|
Administration route |
None |
Dosage |
1E6 cells/kg |
Donor type |
Autologous|Allogeneic |
Pts |
3 |
Age |
Child, Adult |
Lymph depletion |
Yes |
Outcome |
0/3(CR).No Dose-limiting toxicities |
Adverse reactions |
1/3(≥Grade 3 CRS) |
References |
DOI:
10.1182/blood-2023-179667
|
|
Cohort3: dose level 3
|
Administration route |
None |
Dosage |
3E6 cells/kg |
Donor type |
Autologous|Allogeneic |
Pts |
7 |
Age |
Child, Adult |
Lymph depletion |
Yes |
Outcome |
0/7(CR).1 subject experienced DLT (grade 4 CRS) |
Adverse reactions |
2/7(≥Grade 3 CRS) |
References |
DOI:
10.1182/blood-2023-179667
|
|
Cohort4: dose level 4
|
Administration route |
None |
Dosage |
1E7 cells/kg |
Donor type |
Autologous|Allogeneic |
Pts |
6 |
Age |
Child, Adult |
Lymph depletion |
Yes |
Outcome |
2/6(CR).1 subject experienced a prolonged grade 3 CRS (> 72 hours) and grade 3 ICANS, both constituting DLT and necessitating expansion of the cohort without additional DLTs seen. |
Adverse reactions |
1/6(≥Grade 3 CRS) |
References |
DOI:
10.1182/blood-2023-179667
|
|