Cohort1: dose level 1
|
Administration route |
intravenous infusion |
Dosage |
1E6 cells |
Donor type |
Autologous |
Pts |
3 |
Age |
Adult, Older_Adult |
Lymph depletion |
Yes |
Outcome |
3/3(PD) |
Adverse reactions |
1/3(Gastrointestinal disorders) |
|
Cohort2: dose level 2
|
Administration route |
intravenous infusion |
Dosage |
3E6 cells |
Donor type |
Autologous |
Pts |
3 |
Age |
Adult, Older_Adult |
Lymph depletion |
Yes |
Outcome |
1/3(SD); 2/3(PD) |
Adverse reactions |
2/3(Respiratory, thoracic and mediastinal disorders; Platelet count decreased) |
|
Cohort3: dose level 3
|
Administration route |
intravenous infusion |
Dosage |
1E7 cells |
Donor type |
Autologous |
Pts |
3 |
Age |
Adult, Older_Adult |
Lymph depletion |
Yes |
Outcome |
3/3(PD) |
Adverse reactions |
no any CAR-T-related severe events |
|
Cohort4: dose level 4
|
Administration route |
intravenous infusion |
Dosage |
3E7 cells |
Donor type |
Autologous |
Pts |
3 |
Age |
Adult, Older_Adult |
Lymph depletion |
Yes |
Outcome |
3/3(PD) |
Adverse reactions |
1/3(Lymphocyte count decreased) |
|
Cohort5: dose level 5
|
Administration route |
intravenous infusion |
Dosage |
1E8 cells |
Donor type |
Autologous |
Pts |
3 |
Age |
Adult, Older_Adult |
Lymph depletion |
Yes |
Outcome |
3/3(PD) |
Adverse reactions |
1/3(All-cause mortality); 2/3(Blood and lymphatic system disorders; Lymphocyte count decreased) |
|