This is a prospective, single-arm, single-center clinical study designed to evaluate the safety of autologous hematopoietic stem cell infusion for the treatment of prolonged cytopenia following CAR-T cell therapy. Approximately 20 patients will be enrolled.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Autologous hematopoietic stem cell infusion (0.5-3.0×10\^6/kg)
Institute of Hematology and Blood Diseases Hospital Chinese Academy of Medical Sciences
Tianjin, Tianjin Municipality, China
RECRUITINGChanges in Neutrophil Counts After Autologous Stem Cell Infusion
Evaluate changes in neutrophil counts following autologous hematopoietic stem cell infusion.
Time frame: up to 6 months after infusion
Changes in Platelet Counts After Autologous Stem Cell Infusion
Evaluate changes in platelet counts following autologous hematopoietic stem cell infusion.
Time frame: up to 6 months after infusion
Changes in Hemoglobin Levels After Autologous Stem Cell Infusion
Evaluate changes in hemoglobin levels following autologous hematopoietic stem cell infusion.
Time frame: up to 6 months after infusion
Incidence and Severity of Adverse Events Following Autologous Stem Cell Infusion
Assess safety by monitoring infusion-related adverse events, graded according to CTCAE v5.0.
Time frame: up to 6 months after infusion
Incidence of Infections After Autologous Stem Cell Infusion
Evaluate the frequency and types of infections following stem cell infusion, including bacterial, viral, and fungal infections.
Time frame: up to 6 months after infusion
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