Mitral regurgitation after anthracycline treatment for childhood malignancy
J Allen1, J D Thomson, I J Lewis
1Department of Paediatric Cardiology, Yorkshire Heart Centre, E Floor, Jubilee Wing, Leeds General Infirmary, Great George Street, Leeds LS1 3EX, UK.
Insights
Anthracycline chemotherapy can cause new mitral regurgitation (MR) in children, detected by echocardiography. This early MR, along with ECG changes, may predict later heart damage (anthracycline cardiomyopathy).
Area of Science:
- Cardiology
- Oncology
- Pharmacology
Background:
- Anthracyclines are widely used chemotherapy agents for childhood cancers.
- Cardiotoxicity is a known side effect of anthracycline treatment.
- Early detection of cardiac damage is crucial for managing treatment and improving outcomes.
Purpose of the Study:
- To investigate the incidence of new-onset mitral regurgitation (MR) following anthracycline therapy in pediatric patients.
- To assess the relationship between MR and other indicators of myocardial damage.
- To determine if MR can serve as an early predictor of anthracycline-induced cardiomyopathy.
Main Methods:
- Prospective echocardiographic and electrocardiographic study of 305 pediatric patients (aged 2-33 years) treated with anthracyclines.
- Utilized color flow Doppler to detect MR and assessed left ventricular function indices.
- Compared MR prevalence in treated patients to a normal control group.
Main Results:
- 11.6% of patients developed ultrasound-detectable MR post-anthracycline treatment, significantly higher than the 1.8% in controls (p < 0.0001).
- Nine patients also showed non-specific T wave abnormalities on ECG.
- While initial systolic function was normal, four patients later developed impaired left ventricular function.
Conclusions:
- New mitral regurgitation is significantly more prevalent in patients treated with anthracyclines.
- Echocardiographic detection of MR, with or without ECG abnormalities, may be an early indicator of anthracycline cardiomyopathy.
- This finding highlights the importance of cardiac monitoring in pediatric cancer survivors.
Objective:
To investigate the new onset of mitral regurgitation in patients with otherwise normal echocardiograms after anthracycline treatment and to assess its relation to other selected indicators of myocardial damage.
Design:
Prospective echocardiographic and electrocardiographic study.
Setting:
Tertiary paediatric cardiac referral centre.
Patients:
305 patients, aged 2-33 years (median 14 years), treated with cumulative anthracycline doses of between 150-450 mg/m(2) (median 180 mg/m(2)) for childhood malignancy.
Main Outcome Measures:
Colour flow Doppler detection of mitral regurgitation and its relation to changes in echocardiographic indices of left ventricular function (systolic and diastolic dimensions, fractional shortening) and to changes in the 12 lead ECG; and the prevalence of mitral regurgitation in the anthracycline treated patients in comparison with previously studied normal volunteers of similar age.
Results:
34 patients (11.6%) developed ultrasound detectable mitral regurgitation, which was not apparent clinically, during or after anthracycline treatment, compared with only 1.8% of a normal population of similar age (p < 0.0001). Nine of the 34 also developed non-specific T wave abnormalities. All 34 patients had normal systolic function at the time of initial detection of mitral regurgitation, but four later developed impaired left ventricular function (5, 11, 20, and 27 months after the first detection of mitral regurgitation).
Conclusions:
Mitral regurgitation occurs much more often in patients treated with anthracyclines than in the normal population. Echocardiographic detection of new mitral regurgitation with or without ECG abnormalities may be an early predictor of anthracycline cardiomyopathy.
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