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Early Assessment of Anthracycline-induced Cardiotoxicity (CARDIOTOX)

Early Assessment of Anthracycline-induced Cardiotoxicity: Usefulness of Biochemical Markers and Ventricular Function Assessment.

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00195897
Enrollment
6
Registered
2005-09-20
Start date
2006-01-31
Completion date
2009-12-31
Last updated
2016-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure, Congestive, Lymphoma

Keywords

Lymphoma, Anthracyclines, Heart Failure, Radionuclide, Magnetic Resonance Imaging, Troponin, Natriuretic Peptide, Brain

Brief summary

Anthracycline-based chemotherapy is a key point of the treatment of patients with Hodgkin's and non-Hodgkin's lymphomas. However, cumulative doses are limited by cardiotoxicity, resulting in a marked left ventricular function impairment that may lead to heart failure. The standard clinical approach to monitoring for anthracycline cardiotoxicity is based on cardiac function monitoring using echocardiography or radionuclide angiography. The aim of this study is to evaluate the usefulness of biochemical markers of cardiac injury (troponin and NT-proBNP) and structural changes on cardiac MR in predicting anthracycline cardiotoxicity.

Interventions

None listed

Sponsors

Ligue contre le cancer, France
CollaboratorOTHER
Centre Henri Becquerel
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Histologically proven lymphoma (Hodgkin's or non-Hodgkin's) * Age \> 18 y/o and \< 70 y/o * WHO score \< or = 2 * Life expectancy \> 6 mo * Left ventricular ejection fraction \> 50% * Informed consent

Exclusion criteria

* Previous chemotherapy using anthracyclines * History of radiation therapy * History of congestive heart failure * History of chronic renal insufficiency * Contra indication to MR examination * Atrial fibrillation and significant arrhythmia * Pregnancy

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026