Clinical Trial

Early Prophylactic Donor Lymphocyte Infusion After Allo-HSCT for Patients With AML

Study acronym: ELIT-AML01
Active, Not Recruiting Phase 2
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Summary
Allogeneic hematopoietic stem cell transplantation (Allo-HSCT) is a curative option for patients with acute myeloid leukemia (AML). However, transplantation related toxicity and mortality as well as the existence of HLA identical sibling donor represent major limitations. Over the 20 past years, the development of reduced intensity conditioning (RIC) regimen and the use of alternative donors allowed extending the possibility of Allo-HSCT for AML, with decreased toxicity and mortality. This invited to propose this strategy to more advanced patients, making that AML recurrence has become one of the main issues after Allo-HSCT. Thus, to develop prophylactic and preemptive strategies to minimize disease recurrence after Allo-HSCT is now the main challenge in the field. Among cellular and/or pharmacological treatments after Allo-HSCT, donor lymphocyte infusion (DLI) is probably one of the most commonly used treatments after Allo-HSCT. Indeed, DLI were reported as a potential efficient immunotherapy more than 20 years ago for the treatment of patients with leukemia relapsing after Allo-HSCT. However, most of experiences were reported in the setting of relapse after Allo-HSCT and no prospective evaluation of prophylactic DLI is available so far. Thus no strong recommendation for the use of DLI after Allo-HSCT can be made. Our study proposal would like to assess the question of prophylactic DLI efficacy, as a proof of concept of early immune intervention after Allo-HSCT. The investigators, therefore, designed a prospective multicenter randomized trial evaluating the impact of early DLI on outcome after Allo-HSCT for AML.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2018-07-23; most recent amendment 2025-06-13.
Status change: Recruiting → Active, Not Recruiting 2025-06-13
Status change: Not Yet Recruiting → Recruiting 2024-10-03
Trial Details
NCT Number NCT03597321
Lead Sponsor Institut Paoli-Calmettes
Conditions Acute Myeloid Leukemia
Enrollment 124 participants
Start Date 2020-09-07
Primary Completion 2027-05 (estimated)
Study Completion 2028-05 (estimated)
Updated on ClinicalTrials.gov 2025-06-15