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CD19 Chimeric Antigen Receptor T-Cell Therapy Versus Donor Lymphocyte Infusion for Minimal Residual Disease in Patients With Ph-Negative Acute B-Lymphoblastic Leukemia After Hematopoietic Stem Cell Transplantation: A Prospective, Open-Label, Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

This prospective, open-label randomized controlled trial compares CD19 CAR-T therapy with chemotherapy plus donor lymphocyte infusion (DLI) in 70 patients with Ph-negative B-cell acute lymphoblastic leukemia (B-ALL) who exhibited minimal residual disease (MRD) positivity (≥0.1% CD19+ abnormal B cells) after allogeneic hematopoietic stem cell transplantation (HSCT). Patients (aged 3-\<80 years, ECOG 0-2, no relapse, adequate organ function) were randomized to receive either autologous CD19 CAR-T cells following lymphodepletion or conventional chemotherapy with DLI. The primary endpoint is the MRD negativity rate at 3 months. Secondary endpoints include 1-year MRD positivity, relapse rate, overall survival, disease-free survival, GVHD incidence, GVHD-free relapse-free survival, and duration of severe hematological toxicity. The study includes a 1-year follow-up and permits crossover to the alternative treatment for patients with persistent MRD (≥0.1%) at 3 months in the absence of relapse.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 3
Maximum Age: 79
Healthy Volunteers: f
View:

• age 3-\<80 years

• ECOG performance status 0-2

• post-HSCT MRD positivity (≥0.1% CD19+ abnormal B cells by flow cytometry)

• no hematological/extramedullary relapse

• adequate organ function

• negative pregnancy test (for fertile females)

Locations
Other Locations
China
Peking University People's Hospital
RECRUITING
Beijing
Contact Information
Primary
Jing Liu, Doctor
greenimp@163.com
8610-88326900
Time Frame
Start Date: 2025-11-30
Estimated Completion Date: 2028-12-30
Participants
Target number of participants: 70
Treatments
Experimental: CAR-T group
Autologous CD19 CAR-T (1.0×10⁶/kg, single IV infusion) after cyclophosphamide + fludarabine lymphodepletion (no bridging chemo).
Active_comparator: Control group
Chemotherapy + DLI
Sponsors
Leads: Peking University People's Hospital

This content was sourced from clinicaltrials.gov

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