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Abstract: SA-PO0216

Cancer Treatment-Associated Hypomagnesemia: Analysis from a Large Pharmacovigilance Database

Session Information

Category: Onconephrology

  • 1700 Onconephrology

Authors

  • Klomjit, Nattawat, Division of Nephrology and Hypertension, Department of Medicine, University of Minnesota, Minneapolis, Massachusetts, United States
  • Evans, Rich, University of Minnesota Masonic Cancer Center, Minneapolis, Minnesota, United States
  • Pirovano, Marta, Division of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, United States
  • Ortega, Jessica L., Division of Renal Medicine, Department of Medicine, Brigham and Women’s Hospital, Boston, Massachusetts, United States
  • Alikhan, Firasat Mir, Division of Renal Medicine, Department of Medicine, Brigham and Women’s Hospital, Boston, Massachusetts, United States
  • Chewcharat, Api, Division of Renal Medicine, Department of Medicine, Brigham and Women’s Hospital, Boston, Massachusetts, United States
  • Chowdhury, Raad Bin Zakir, Division of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, United States
  • Sise, Meghan E., Division of Nephrology, Department of Internal Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States
  • Jhaveri, Kenar D., Division of Kidney Diseases and Hypertension, Donald and Barbara Zucker School of Medicine, Boston, Massachusetts, United States
  • Gupta, Shruti, Division of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, United States
Background

Hypomagnesemia is common in patients with cancer; however, there is a lack of real-world data on its frequency in the setting of older and newer antineoplastic agents.

Methods

We utilized VigiBase to examine the frequency of hypomagnesemia after treatment with anti-epidermal growth factor receptor (EGFR) monoclonal antibodies (anti-EGFR mABs), anti-EGFR tyrosine kinase inhibitors (anti-EGFR TKIs), anti-human epidermal growth factor receptor 2 (HER2) monoclonal antibodies (anti-HER2 mABs), and conventional chemotherapy. The strength of association was determined using information component (IC), a measure of disproportionality between observed and expected number of reports for a drug-event combination. A positive IC025 indicates that the number of observed reports exceeded the expected reports.

Results

Between 2010-2024, there were 18,388 reports of antineoplastic-associated hypomagnesemia in 2226 individuals. The drugs with the highest IC025 were panitumumab (6.22), cetuximab (4.85), and cisplatin (3.26) (Figure). Hypomagnesemia was reported most commonly after conventional chemotherapy (n=896, 48.6%) and anti-EGFR mABs (n=769, 41.7%). Time to hypomagnesemia was shortest following conventional chemotherapy (18.3 days, IQR 7-50) and longest in those receiving anti-EGFR mABs (77.5 days, IQR 28-182.1). Gastrointestinal and hepatobiliary cancers (40.1%) were the most common types of cancer, followed by lung (14.1%), and head and neck cancer (13.4%).Time to onset of hypomagnesemia was the shortest in those in the lowest age group (≤17 years).

Conclusion

Hypomagnesemia was most frequent with conventional chemotherapy and anti-EGFR mABs; thus, patients treated with these agents should be monitored for hypomagnesemia, and may benefit from preventative or therapeutic strategies.

Funding

  • NIDDK Support

Digital Object Identifier (DOI)