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Recruiting 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

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07899840). StuddyBuddy aggregates publicly available trial information.