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Research · 02 of 05

Intravenous magnesium lowered kidney injury markers during weekly cisplatin

Keep magnesium replacement in cisplatin protocols; this trial's benefit is on biomarkers, not proven renal outcomes.

Design
Randomised controlled trial, four arms
Population
100 patients with head and neck SCC on weekly cisplatin and radiotherapy
Primary outcome
Urinary and serum kidney injury biomarkers
Effect
Lower urinary KIM-1 and NGAL with magnesium (P < 0.05)

An Egyptian trial randomised 100 patients with newly diagnosed head and neck squamous cell carcinoma, all having weekly cisplatin 40 mg/m² with radiotherapy for seven cycles, to no magnesium or to 1 g, 2 g or 3 g of intravenous magnesium sulphate with each cycle.

Magnesium groups had lower urinary KIM-1 and NGAL, markers of tubular injury, than controls. The 3 g group also had lower serum soluble Fas ligand and malondialdehyde. Clinical renal outcomes such as creatinine-defined kidney injury or dose reductions were not reported in the abstract.

Magnesium supplementation with cisplatin is already common because cisplatin wastes magnesium. This trial suggests a possible protective effect on the tubule, but only through biomarkers, so it supports existing practice rather than changing it.

  • Check serum magnesium, creatinine and electrolytes before each cisplatin cycle
  • Replace magnesium as per your oncology protocol
  • Ensure adequate pre- and post-hydration with cisplatin
  • Watch for hypomagnesaemia-related arrhythmia and tetany

Why it matters

Supports routine magnesium with cisplatin in a setting where head and neck cancer is common, including India.

Don't overread it

Only surrogate biomarkers were reported; it does not show fewer clinical kidney injuries.

The statistics, in plain English

KIM-1 and NGAL are early markers of kidney tubule injury; lower levels are encouraging but are surrogate endpoints. With 25 patients per arm, the trial is too small to show differences in clinical kidney injury.

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