Key result
Early dapagliflozin is linked to ~2-point better 12-month global longitudinal strain during anthracycline-trastuzumab chemotherapy.
Why the study?
Subclinical cardiac dysfunction during cardiotoxic anticancer therapy may develop, but the impact of early cardioprotective intervention with dapagliflozin in routine practice remains unclear.
Does early dapagliflozin initiation prevent subclinical changes in cardiac function over 12 months in patients receiving anthracycline-trastuzumab therapy for HER2-positive breast cancer?
Cohort (n=149)
Yes
Does early dapagliflozin initiation prevent subclinical changes in cardiac function over 12 months in patients receiving anthracycline-trastuzumab therapy for HER2-positive breast cancer?
Early initiation of dapagliflozin in patients receiving cardiotoxic anthracycline-trastuzumab therapy is associated with better preservation of left ventricular mechanics and attenuation of left atrial remodeling over 12 months.
Hypothesis-generating for early dapagliflozin to preserve LV mechanics on anthracycline-trastuzumab; prospective trials needed before clinical adoption.
Background Subclinical cardiac dysfunction involving myocardial deformation, diastolic mechanics, left atrial (LA) remodeling may develop during cardiotoxic anticancer therapy, while the impact of early cardioprotective intervention in routine practice remains unclear. Aim To evaluate the association between early dapagliflozin initiation and 12-month subclinical changes in left ventricular (LV) mechanics and LA structure and function during anticancer therapy. Methods This multicenter retrospective study included 149 patients with HER2-positive breast cancer treated with anthracycline-based chemotherapy followed by trastuzumab across four centers. Dapagliflozin 10 mg once daily was prescribed at the treating physician’s discretion. Patients were classified as early dapagliflozin (≤3 months; n=67) versus no dapagliflozin use (n=82). Transthoracic echocardiography was performed at baseline, 6, 12 months. LV global longitudinal strain (GLS), tissue Doppler e′ velocities, average E/e′, LV ejection fraction (LVEF), indexed LA volumes (LAVmax, LAVmin) with total LA emptying function (LAEF) were assessed. Longitudinal changes were analyzed using linear mixed-effects models adjusted for baseline variables. Results Baseline clinical and echocardiographic characteristics were comparable between groups. Over 12 months, GLS deteriorated from −20.3 ± 1.9% to −17.9 ± 2.1% in the early dapagliflozin group, compared with −19.6 ± 2.1% to −15.8 ± 2.5% in patients without dapagliflozin (p<0.001). Average E/e′ increased from 9.8 ± 2.0 to 12.5 ± 2.4 versus 10.6 ± 2.3 to 15.3 ± 2.9, respectively (p<0.001). LAEF declined from 62.1 ± 7.8% to 56.2 ± 7.9% with early dapagliflozin and to 47.1 ± 9.8% without dapagliflozin (p<0.001). Indexed LAVmin increased from 9.5 ± 3.8 to 13.0 ± 4.5 ml/m² versus 10.8 ± 4.1 to 18.1 ± 5.8 ml/m², respectively (p<0.001). LVEF remained within the normal range in both groups throughout follow-up. Conclusion Early dapagliflozin initiation during anthracycline–trastuzumab therapy was associated with better preservation of LV mechanics and LA remodeling over 12 months.
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Hazarapetyan et al. (2026) conducted a cohort in HER2-positive breast cancer (n=149). Early dapagliflozin initiation (≤3 months) vs. No dapagliflozin use was evaluated on 12-month subclinical changes in left ventricular (LV) mechanics (global longitudinal strain) and left atrial structure and function (p=<0.001). Early dapagliflozin initiation during anthracycline-trastuzumab therapy was associated with better 12-month preservation of LV mechanics, including global longitudinal strain (-17.9% vs -15.8%; p<0.001).
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