Lenvatinib Linked to Nephrotic Syndrome in VHL Syndrome: Case Highlights Rare Kidney Complication
China: A recently published case report in BMC Nephrology by Dr. Yuehong Li and colleagues from the Department of Nephrology, Beijing Tsinghua Changgung Hospital, sheds light on a rare but serious complication associated with the cancer drug lenvatinib (LEN). The report presents a case of nephrotic syndrome triggered by LEN therapy in a patient with von Hippel-Lindau (VHL) syndrome, underscoring the need for close renal monitoring in individuals undergoing tyrosine kinase inhibitor (TKI) treatment.
VHL syndrome is a rare inherited disorder marked by the development of tumors in multiple organs. TKIs like lenvatinib are increasingly used for managing VHL-associated tumors, including pancreatic neuroendocrine tumors (pNET). However, LEN is known to carry a risk of renal side effects, most notably proteinuria.
The patient in the report, a 50-year-old Chinese man with genetically confirmed VHL syndrome, developed swelling in the lower limbs and foamy urine—classic symptoms of nephrotic syndrome—two years after beginning LEN therapy for pNET. Laboratory investigations revealed massive proteinuria, low serum albumin, and elevated cholesterol levels. Renal biopsy results showed thrombotic microangiopathy (TMA) and focal segmental glomerulosclerosis (FSGS)-like lesions, both indicative of severe kidney damage.
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