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E-Poster Display

292P - Evaluation of the cardioprotective effects of l-carnitine and silymarin in cancer patients receiving anthracycline-containing chemotherapy

Date

17 Sep 2020

Session

E-Poster Display

Topics

Cytotoxic Therapy

Tumour Site

Breast Cancer

Presenters

Zeinab Zalat

Citation

Annals of Oncology (2020) 31 (suppl_4): S348-S395. 10.1016/annonc/annonc268

Authors

Z. Zalat1, M.A. Alm El-Din2, N.A.E.M. Kohaf1, M. Abdel-Latif3, H. Elewa4

Author affiliations

  • 1 Clinical Pharmacy, Faculty of pharmacy, Al Azhar University, 11321 - Cairo/EG
  • 2 Clinical Oncology, Faculty of Medicine, Tanta University, 31511 - Tanta/EG
  • 3 Clinical Pharmacy, Faculty of Pharmacy, Assiut University, Assiut/EG
  • 4 Pharmacy Practice, Faculty of Pharmacy, Horus University, Dominate/EG

Resources

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Abstract 292P

Background

Anthracycline-induced cardiotoxicity is the most common constraint of its use in the treatment of various types of cancer. This study aimed to investigate the benefits of adding L-carnitine and silymarin compared to anthracycline chemotherapy alone in patients with cancer.

Methods

83 patients were recruited from the Clinical Oncology Department, Tanta University, Egypt, and prospectively randomized to receive their anthracycline-containing therapeutic regimen, control group (n=33), anthracycline plus L-carnitine, L-carnitine group (n=25), or anthracycline plus silymarin, silymarin group (n= 25). Blood samples were collected at begging and after 6 months to measure LDH, CK-MB, cTn I, Anticardiolipin IgG, Fe, ferritin, and TIBC, and % of saturation. % EF was documented. Data were statistically analyzed by ANOVA and paired t-test. P <0.05 was statistically significant.

Results

The obtained data suggested that adding L-carnitine to anthracycline chemotherapy had a significant beneficial effect on %EF (p=0.003), anticardiolipin IgG (P=0.000), ferritin (P=0.000) , and TIBC(P=0.011) , and that adding silymarin to anthracycline chemotherapy had a significantly beneficial effect on anticardiolipin IgG (P=0.000), iron (p=0.001),ferritin (p= 0.000), TIBC (p=0.007) , and % saturation (p=0.001) silymarin group showed a significant decrease in iron profile compared to the L-carnitine group, supporting the hypothesis of silymarin iron chelating activity.

Conclusions

The co-administration of L-carnitine or silymarin with anthracycline-containing chemotherapy represents a new therapeutic strategy, especially silymarin, for better control of anthracycline-induced cardiotoxicity, as silymarin resulted in more beneficial effects on iron profile compared to anthracycline alone and anthracycline with L-carnitine.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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