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Published on: February 3, 2014
Right ventricular function during trastuzumab therapy for breast cancer
Géris Mazzutti1,2, Fernando Pivatto Júnior3, Guilherme Oliveira Magalhães Costa4
1Cardiology Division, Hospital de Clínicas de Porto Alegre (HCPA), Rua Ramiro Barcelos, 2350, Room 2061, Porto Alegre, RS, 90035-903, Brazil. gmazzutti@hcpa.edu.br.
Trastuzumab (TTZ) therapy can cause cardiotoxicity. This study found that while right ventricular (RV) function decreased during TTZ treatment, this decline was not linked to left ventricular (LV) cardiotoxicity in breast cancer patients.
Area of Science:
- Cardiology
- Oncology
- Pharmacology
Background:
- Cardiotoxicity (CDT) is a significant adverse effect of trastuzumab (TTZ) therapy in breast cancer patients.
- The specific impact of TTZ on right ventricular (RV) function and its association with subclinical cardiotoxicity remains unclear.
Purpose of the Study:
- To longitudinally assess changes in RV function during TTZ treatment.
- To determine if alterations in RV function are associated with subclinical cardiotoxicity in patients receiving TTZ.
Main Methods:
- Echocardiograms were performed on 25 breast cancer patients at baseline and every 3 months for one year during TTZ therapy.
- Subclinical cardiotoxicity was defined as a ≥12% relative reduction in left ventricular global longitudinal strain (LV GLS).
- Evaluated parameters included LV ejection fraction, LV GLS, RV GLS, and RV Fractional Area Change.
Main Results:
- A significant decrease in LV ejection fraction and a gradual decline in LV GLS were observed during TTZ therapy.
- RV GLS decreased significantly at 3 and 6 months, and RV Fractional Area Change was lower at 6 months.
- Subclinical cardiotoxicity was identified in 52% of patients, but worsening RV parameters did not differ between those with and without subclinical cardiotoxicity.
Conclusions:
- Right ventricular function shows a decline during trastuzumab therapy.
- The observed decrease in RV function during TTZ treatment was not associated with subclinical left ventricular cardiotoxicity in this patient cohort.
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