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NCT07899840
Establishment of a Novel Flow Cytometric Diagnostic Assay to Effectively Evaluate Immune Reconstitution After Hematopoietic Stem Cell Transplantation for Acute Lymphoblastic Leukemia
Conditions: Acute Lymphobkastic Leukemia
Sex: All
Healthy volunteers: No
Enrollment: 150
Sponsor: Fondazione Matilde Tettamanti Menotti De Marchi Onlus
Location: Saint Anna Kinderspital Vienna
Summary
Primary Objective
To assess immune reconstitution during the first 18 months following hematopoietic stem cell transplantation (HSCT) for acute lymphoblastic leukemia (ALL), with a particular focus on the T-cell compartment (thymic regeneration and surrogate markers of cytotoxic function), using a dedicated panel developed within the EuroFlow consortium.
Secondary Objectives
To assess the impact of donor and recipient characteristics, graft-versus-host disease (GvHD) prophylaxis, and conditioning regimen on post-transplant immune reconstitution.
To evaluate the correlation between immune reconstitution and the development of complications using unsupervised analysis.
Eligibility Criteria
Inclusion Criteria:
* Patients who undergo first HSCT for ALL
* Signing of informed consent by the patient (age\>18) or by parent/legal guardian (age \1° HSCT
* ALL with specific genetic backgrounds which may impact on IR such as Down syndrome
Source: ClinicalTrials.gov (NCT07899840). StuddyBuddy aggregates publicly available trial information.