Key result
Vitamin E and levocarnitine cut cardiac events ~24% and lower BNP and CK during doxorubicin therapy.
Why the study?
Doxorubicin induces acute and chronic cardiotoxicity, prompting evaluation of vitamin E and levocarnitine as cardioprotective agents in adult breast cancer patients.
Does vitamin E and levocarnitine prophylaxis prevent acute doxorubicin cardiotoxicity in female adult breast cancer patients?
RCT (n=74)
randomly assigned
Does vitamin E and levocarnitine prophylaxis prevent acute doxorubicin cardiotoxicity in female adult breast cancer patients?
p-value: p=<0.001
Prophylactic use of vitamin E and levocarnitine significantly reduces cardiac enzyme elevation and cardiac events in breast cancer patients undergoing doxorubicin chemotherapy.
Supports vitamin E and levocarnitine prophylaxis to lower acute doxorubicin cardiotoxicity risk; extends RCT evidence for adjunctive cardioprotection in breast cancer.
Background Doxorubicin induces acute and chronic cardiotoxicity. This study is aimed to evaluate the efficacy and safety of vitamin E and levocarnitine (EL) as cardioprotective agents against acute doxorubicin cardiotoxicity in female adult breast cancer patients. Methods A prospective, randomized controlled study was conducted in patients treated with doxorubicin and cyclophosphamide (AC). Patients were randomly assigned to EL plus AC or AC alone for the duration of 4 cycles. Cardiac enzymes (B-type natriuretic peptide, creatine kinase, troponin I (Trop)) and cardiac events were monitored during treatment to evaluate the cardioprotective efficacy of EL. Results Seventy-four patients were recruited and received four cycles of chemotherapy. The intervention group ( n = 35) showed a significant reduction in both the B-type natriuretic peptide and creatine kinase cardiac enzymes compared to the control group ( n = 39). The median (IQR) change for BNP was 0.80 (0.00–4.00) for IG versus 1.80 (0.40–3.60) for CG groups ( p < 0.001); creatine kinase was −0.08 (−0.25–0.05) for IG versus 0.20 (0.05–0.50) for CG ( p < 0.001). The addition of EL decreased the cardiac events by 24.2% ( p = 0.02). All adverse events were tolerable and manageable. Conclusion This study supports the addition of EL as prophylaxis against acute doxorubicin cardiotoxicity and it was also very well tolerated by a majority of the patients. The co-administration of EL at higher doxorubicin (240 mg/m 2 ) dose should be further investigated.
No takes yet. Share an insight, caveat, or question.
Moustafa et al. (2023) conducted an RCT in breast cancer (n=74). vitamin E and levocarnitine vs. control (chemotherapy alone) was evaluated on Cardiac enzymes (B-type natriuretic peptide, creatine kinase, troponin I) and cardiac events (p=<0.001). Vitamin E and levocarnitine prophylaxis significantly reduced B-type natriuretic peptide and creatine kinase levels (p<0.001) and decreased cardiac events by 24.2% (p=0.02) during doxorubicin therapy.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: