Clinical Trial

Cardiovascular Complications in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation.

Study acronym: ALLOCARDIOTOX
Not Yet Recruiting
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Summary
Allogeneic hematopoietic stem cell transplantation (HSCT) represents a major therapeutic strategy for malignant hematologic diseases, with the number of procedures steadily increasing in France each year. Conditioning and maintenance regimens carry a risk of both short- and long-term cardiotoxicity, leading to serious cardiovascular events including acute coronary syndrome (ACS), cardiac dysfunction, arrhythmias, pulmonary hypertension, and pericardial effusion. The pathophysiology of cardiotoxicity in HSCT patients remains poorly understood. It is therefore crucial to investigate underlying mechanisms and identify predictive factors of cardiotoxicity in order to provide appropriate cardiological follow-up and management. Current European Society of Cardiology guidelines recommend routine monitoring of HSCT patients with echocardiography and cardiac biomarkers (NT-proBNP, troponin), although these recommendations are based on small-scale studies. The cardiodepressor factor DPP3 has shown promising results in cardio-oncology, with a causal role in anthracycline-induced cardiac dysfunction. Its role in HSCT-related cardiotoxicity requires further evaluation. This multicenter study of HSCT recipients will be a valuable resource, enabling a better understanding of the pathophysiology of cardiotoxicity and prognosis. It will highlight imaging (echocardiography, calcium score, supra-aortic Doppler), electrocardiographic, and biological markers (including DPP3) associated with prognosis.
Trial Details
NCT Number NCT07157670
Lead Sponsor Assistance Publique - Hôpitaux de Paris
Collaborators: INSERM UMR-S 942 MASCOT, INSERM U1086 Cancers et Préventions, Fédération Française de Cardiologie
Conditions Cardiotoxicity, DPP3, HSCT, Allogeneic Hematopoietic Stem Cell Transplantation, ACS - Acute Coronary Syndrome, Cardiac Dysfunction, Arrythmia, Cardiac, Pulmonary Hypertension +1 more
Enrollment 400 participants
Start Date 2025-09-15
Primary Completion 2027-12-25 (estimated)
Study Completion 2028-09-15 (estimated)
Updated on ClinicalTrials.gov 2025-09-05