References |
Design |
Cases |
Treatment aims |
Diagnostic criteria |
Conclusion |
Kalay et al. [80] |
Randomized controlled study |
25 patients |
Carvedilol vs. placebo |
LVEF, systolic and diastolic |
Prophylactic use of carvedilol in pts with anthracycline protects both systolic and diastolic functions of LV |
Kaya et al. [81] |
Prospective randomized controlled trial |
45 patients with breast cancer |
Nebivolol vs. placebo |
Change in LVEF from baseline, N-terminal brain natriuretic peptide. |
LVEF change; pre/post placebo: 66.6%/57.5%; nebivolol: 65.6%/63.8%. Nebivolol protects the myocardium against anthracycline-induced cardiotoxicity |
Seitan et al. [82] |
Follow-up study |
920 patients with breast cancer |
Beta-blockers |
LVEF, HF incidence |
Continuous use of BB lowers the incidence of HF in patients |
Gulati et al. [83] |
Randomized controlled study |
130 women with breast cancer |
Candesartan vs. metoprolol vs. candesartan+metoprolol |
Change in LVEF on completion of adjuvant therapy |
Mean LVEF % point reduction: placebo:2.6; candesartan:0.8; metoprolol:1.6. Concomitant treatment with candesartan protects against an early decline in LVEF |
Pitkin et al. [84] |
Randomized controlled study |
33 petients with HER2-positive early breast cancer |
Perindopril vs. bisoprolol vs. placebo |
Change in LV volume and LVEF |
No difference in the primary outcome |
Cardinale et al. [23] |
Clinical trial |
201 patients with LVEF <45% due to anthracycline-induced cardiomyopathy |
Enalapril vs. no treatment |
Recovery in LVEF |
Cardiotoxicity incidence control 25/58 (43%), enalapril 0/56 (0%) |