This is a prospective, descriptive study designed to assess the feasibility of administering CAR T therapy among patients with moderate to severe renal impairment using dose adjusted lymphodepleting chemotherapy.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Received IV on Days -5 to -3 before CAR T cell therapy
Received IV on Days -5 to -3 before CAR T cell therapy
Caitlin Guzowski
Atlanta, Georgia, United States
RECRUITINGOccurrence of CRS
Collection of maximum grade of CRS (based on CTCAE v5) and when this event occurs post CAR T cell therapy infusion
Time frame: 90 days
Occurrence of ICANS
Collection of maximum grade of ICANs (based on CTCAE v5) and when this event occurs after CAR T cell therapy infusion
Time frame: 90 days
Occurrence of Cytopenias
Collection of grade 3 or higher (based on CTCAE v5) cytopenias not resolved by Day 30 post CAR T cell infusion
Time frame: 90 days
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