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Adverse kidney effects of epidermal growth factor receptor inhibitors
Hassan Izzedine1, Mark A Perazella2
1Department of Nephrology, Monceau Park International Clinic, Paris, France.
Abstract:
The epidermal growth factor receptor (EGFR) is implicated in various malignancies. The past decade has seen the development and widespread use of EGFR inhibitors for the successful treatment of such cancers. Available EGFR inhibitors include small molecule tyrosine-kinase inhibitors and monoclonal antibodies. Class-related renal adverse events result in dual toxicity including tubular/electrolyte disorders and glomerulopathies. Tubular injury is common and mainly due to monoclonal antibodies while glomerulopathy is rare and related to various anti-EGFR agents. The exact pathogenesis of anti-EGFR agents associated with kidney disorders remains to be elucidated.
Insights
Epidermal growth factor receptor (EGFR) inhibitors treat cancer but can cause kidney damage. Tubular injury is common with monoclonal antibodies, while rare glomerulopathy is linked to various anti-EGFR drugs.
Area of Science:
- Oncology
- Nephrology
- Pharmacology
Background:
- Epidermal growth factor receptor (EGFR) is crucial in many cancers.
- EGFR inhibitors are widely used cancer therapeutics.
- These inhibitors can cause kidney adverse events.
Purpose of the Study:
- To review renal adverse events associated with EGFR inhibitors.
- To differentiate between tubular and glomerular kidney injuries.
- To discuss the pathogenesis of these EGFR inhibitor-induced nephropathies.
Main Methods:
- Literature review of EGFR inhibitors and associated renal toxicities.
- Analysis of reported cases of kidney disorders.
- Categorization of renal adverse events by drug class and affected kidney component.
Main Results:
- EGFR inhibitors, including small molecule tyrosine-kinase inhibitors and monoclonal antibodies, are associated with renal toxicity.
- Tubular/electrolyte disorders are common, primarily linked to monoclonal antibodies.
- Glomerulopathies are rare but associated with various anti-EGFR agents.
Conclusions:
- Anti-EGFR therapies pose a risk of kidney damage.
- Distinct renal toxicities (tubular vs. glomerular) are observed.
- Further research is needed to fully understand the pathogenesis of anti-EGFR-related kidney disorders.
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