Key result
Trastuzumab similarly impairs LV and RV mechanics, with a ~15% RV GLS decline predicting cardiotoxicity.
Why the study?
Trastuzumab can cause cardiotoxicity with LV systolic dysfunction, but its effects on RV function have not been elucidated.
Does trastuzumab therapy impair right ventricular deformation mechanics in women with breast cancer?
Cohort (n=101)
Does trastuzumab therapy impair right ventricular deformation mechanics in women with breast cancer?
Effect estimate: AUC 0.68 (95% CI 0.54-0.81)
Trastuzumab therapy impairs both left and right ventricular deformation mechanics similarly, and early changes in RV global longitudinal strain can predict subsequent cardiotoxicity.
RV GLS changes may aid trastuzumab cardiotoxicity surveillance; hypothesis-generating and should not yet change practice.
BACKGROUND: Trastuzumab improves dramatically the prognosis of HER2-positive breast cancer patients, but it may lead to cardiotoxicity with left ventricular (LV) systolic dysfunction. Its effects on right ventricular (RV) function have not however been elucidated. We sought to assess LV and RV deformation mechanics during treatment with trastuzumab in breast cancer patients. METHODS AND RESULTS: We studied 101 consecutive women (mean age 54.3 ± 11.4 years) receiving trastuzumab for 12 months; 62 of them (61.4%) had previously received anthracyclines and 26 (25.7%) were receiving taxanes concurrently with trastuzumab. Comprehensive two-dimensional echocardiography with speckle tracking imaging of LV and RV global longitudinal strain (GLS) and RV free wall longitudinal strain (FWLS) analyses were performed at baseline and every 3 months up to treatment completion. Cardiotoxicity was defined as a decrease of baseline LV ejection fraction > 10 percentage units to a value < 50%. At 3 months, only LV GLS was significantly reduced (-19.5 ± 2.7 to -18.7 ± 2.8, P = 0.0410), while at 6 months, LV GLS, RV GLS and RV FWLS had significantly declined reaching their lowest values (-17.9 ± 6.1, P = 0.002, -19.6 ± 5.2, P = 0.003 and -19.7 ± 5.6, P = 0.004, respectively). Ten women (9.9%) developed cardiotoxicity. A RV GLS percent change of -14.8% predicted cardiotoxicity with 66.7% sensitivity and 70.8% specificity (area under the curve 0.68, 95% confidence interval 0.54-0.81), classifying correctly 90% of women with cardiotoxicity. This cut-off is quite similar to the 15% change of LV GLS previously suggested as predictive of cardiotoxicity. CONCLUSIONS: Deformation mechanics of both the left and right ventricle follow similar temporal pattern and degree of impairment during trastuzumab therapy, confirming the global and uniform effect of trastuzumab on myocardial function.
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Keramida et al. (2019) conducted a cohort in Breast cancer (n=101). Trastuzumab was evaluated on Cardiotoxicity (decrease of baseline LVEF >10 percentage units to <50%) (AUC 0.68, 95% CI 0.54-0.81). Trastuzumab therapy caused similar declines in left and right ventricular deformation mechanics, with a -14.8% change in RV GLS predicting cardiotoxicity (AUC 0.68; 95% CI 0.54-0.81).
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