Preventive effect of 20 mEq and 8 mEq magnesium supplementation on cisplatin-induced nephrotoxicity: a propensity score-matched analysis
- PMID: 34984552
- DOI: 10.1007/s00520-021-06790-w
Preventive effect of 20 mEq and 8 mEq magnesium supplementation on cisplatin-induced nephrotoxicity: a propensity score-matched analysis
Abstract
Purpose: The protective effect of magnesium (Mg) supplementation against cisplatin (CDDP)-induced nephrotoxicity has been widely described; however, the optimal dose of Mg supplementation is unclear. The aim of this study was to investigate whether 20 mEq of Mg supplementation is more effective than 8 mEq Mg in preventing CDDP-induced nephrotoxicity, as well as the associated risk factors, in cancer patients treated with CDDP-based chemotherapy.
Methods: Pooled data of 272 patients receiving 20 mEq or 8 mEq Mg supplementation to CDDP-based chemotherapy from a multicenter, retrospective, observational study were compared using propensity score matching. Separate multivariate logistic regression analyses were used to identify the risk factors for renal failure induced by each treatment dose.
Results: There was no significant difference in the incidence of nephrotoxicity between the 8 mEq and 20 mEq groups (P = 0.926). There was also no significant difference in the severity of nephrotoxicity, elevated serum creatinine levels, and decreased estimated creatinine clearance levels between the two groups. Cardiac disease and albumin levels were identified as independent risk factors for CDDP-induced nephrotoxicity.
Conclusion: We did not find an advantage of 20 mEq over 8 mEq Mg supplementation in terms of a preventive effect against CDDP-induced nephrotoxicity. The optimal dose of Mg supplementation for the prevention of CDDP-induced nephrotoxicity remains unknown, and further studies are warranted.
Keywords: Cisplatin; Magnesium supplementation; Nephrotoxicity; Renal failure.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
Similar articles
-
Comparison of preventive effects of combined furosemide and mannitol versus single diuretics, furosemide or mannitol, on cisplatin-induced nephrotoxicity.Sci Rep. 2024 May 7;14(1):10511. doi: 10.1038/s41598-024-61245-6. Sci Rep. 2024. PMID: 38714773 Free PMC article.
-
Short hydration with 20 mEq of magnesium supplementation for lung cancer patients receiving cisplatin-based chemotherapy: a prospective study.Int J Clin Oncol. 2020 Nov;25(11):1928-1935. doi: 10.1007/s10147-020-01755-1. Epub 2020 Aug 1. Int J Clin Oncol. 2020. PMID: 32740717 Clinical Trial.
-
Risk Factors for Cisplatin-Induced Nephrotoxicity: A Multicenter Retrospective Study.Oncology. 2021;99(2):105-113. doi: 10.1159/000510384. Epub 2020 Sep 23. Oncology. 2021. PMID: 32966986
-
Molecular mechanisms of cisplatin-induced nephrotoxicity: a balance on the knife edge between renoprotection and tumor toxicity.J Biomed Sci. 2019 Mar 13;26(1):25. doi: 10.1186/s12929-019-0518-9. J Biomed Sci. 2019. PMID: 30866950 Free PMC article. Review.
-
A systematic review for prevention of cisplatin-induced nephrotoxicity using different hydration protocols and meta-analysis for magnesium hydrate supplementation.Clin Exp Nephrol. 2024 Jan;28(1):1-12. doi: 10.1007/s10157-023-02386-2. Epub 2023 Aug 2. Clin Exp Nephrol. 2024. PMID: 37530867 Review.
Cited by
-
Cisplatin in Liver Cancer Therapy.Int J Mol Sci. 2023 Jun 29;24(13):10858. doi: 10.3390/ijms241310858. Int J Mol Sci. 2023. PMID: 37446035 Free PMC article. Review.
-
Comparison of preventive effects of combined furosemide and mannitol versus single diuretics, furosemide or mannitol, on cisplatin-induced nephrotoxicity.Sci Rep. 2024 May 7;14(1):10511. doi: 10.1038/s41598-024-61245-6. Sci Rep. 2024. PMID: 38714773 Free PMC article.
-
Hydration Methods for Cisplatin Containing Chemotherapy: A Systematic Review.Oncologist. 2024 Feb 2;29(2):e173-e186. doi: 10.1093/oncolo/oyad297. Oncologist. 2024. PMID: 37995306 Free PMC article.
-
Risk factor analysis for cisplatin-induced nephrotoxicity with the short hydration method in diabetic patients.Sci Rep. 2023 Oct 10;13(1):17126. doi: 10.1038/s41598-023-44477-w. Sci Rep. 2023. PMID: 37816823 Free PMC article.
References
-
- Hartmann JT, Lipp HP (2003) Toxicity of platinum compounds. Expert Opin Pharmacother 4:889–901. https://doi.org/10.1517/14656566.4.6.889 - DOI - PubMed
-
- Sastry J, Kellie SJ (2005) Severe neurotoxicity, ototoxicity and nephrotoxicity following high-dose cisplatin and amifostine. Pediatr Hematol Oncol 22:441–445. https://doi.org/10.1080/08880010590964381 - DOI - PubMed
-
- Ries F, Klastersky J (1986) Nephrotoxicity induced by cancer chemotherapy with special emphasis on cisplatin toxicity. Am J Kidney Dis 8:368–379. https://doi.org/10.1016/s0272-6386(86)80112-3 - DOI - PubMed
-
- Dobyan DC, Levi J, Jacobs C, Kosek J, Weiner MW (1980) Mechanism of cis-platinum nephrotoxicity: II. Morphologic observations J Pharmacol Exp Ther 213:551–556 - PubMed
-
- Pinzani V, Bressolle F, Haug IJ, Galtier M, Blayac JP, Balmès P (1994) Cisplatin-induced renal toxicity and toxicity-modulating strategies: a review. Cancer Chemother Pharmacol 35:1–9. https://doi.org/10.1007/BF00686277 - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical