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Nephrotic Syndrome Induced by Lenvatinib Treatment for Hepatocellular Carcinoma
Thaninee Prasoppokakorn1, Kessarin Thanapirom1,2,3, Sombat Treeprasertsuk1
1Division of Gastroenterology, Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Abstract:
Lenvatinib, an oral small-molecule multiple tyrosine kinase inhibitor (TKI), has been approved for first-line therapy for unresectable hepatocellular carcinoma (HCC). Proteinuria is one of the most common adverse events associated with lenvatinib treatment. We reported a 67-year-old Thai female was diagnosed with NASH cirrhosis and HCC BCLC B with TACE refractoriness. She received 8 mg of lenvatinib for 2 weeks and began to experience worsening hypertension, bilateral pleural effusion, pedal edema, hypoalbuminemia, hypercholesterolemia, and proteinuria. After exclusion of all possible causes, lenvatinib-induced nephrotic syndrome (NS) was diagnosed. One week after discontinuing the drug, her symptoms gradually improved. To date, there have been only a handful of reported cases of lenvatinib-induced nephrotoxicity. We report herein the case of lenvatinib-induced NS in a cirrhotic patient with HCC with resolution of symptoms in a short period after drug discontinuation. In addition, we reviewed all reported cases of lenvatinib-induced nephrotoxicity.
Insights
Lenvatinib treatment for liver cancer can cause nephrotic syndrome, a kidney disorder. This case study shows symptoms improved after stopping the drug, highlighting lenvatinib-induced kidney toxicity.
Area of Science:
- Oncology
- Nephrology
- Pharmacology
Background:
- Lenvatinib is approved for unresectable hepatocellular carcinoma (HCC).
- Proteinuria is a common side effect of lenvatinib.
- Nephrotoxicity is a known, though infrequent, adverse event of lenvatinib therapy.
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