• Medicine · Jan 2022

    Case Reports

    Dabrafenib- and trametinib-associated glomerular toxicity: A case report.

    • Eunmi Jo and Harin Rhee.
    • Department of Nephrology, Pusan National University School of Medicine, Busan, Republic of Korea.
    • Medicine (Baltimore). 2022 Jan 7; 101 (1): e28485.

    RationaleCombined treatment with dabrafenib, a B-RAF inhibitor, and trametinib, a mitogen-activated protein kinase inhibitor, is an effective option for patients with metastatic melanoma. A few cases of acute kidney injury associated with tubulointerstitial nephritis and 1 case of nephrotic syndrome have been reported in patients on this drug combination; however, progressive renal injury has not been reported. In this case study, we report a patient with metastatic melanoma who developed glomerular capillary endothelial toxicity and progressive glomerular sclerosis during combination therapy.Patient ConcernOur patient was an 80-year-old woman with a history of type 2 diabetes and chronic kidney disease.Diagnosis And InterventionShe was diagnosed with metastatic melanoma and commenced combination therapy with dabrafenib and trametinib.OutcomesHer renal function progressively deteriorated; by month 20 after treatment commencement, her serum creatinine level had increased from 1.59 to 3.74 mg/dL. The first kidney biopsy revealed marked glomerular and endothelial cell damage. Her medication was stopped, but no improvement was evident. At 5 months after the first biopsy, her serum creatinine level had increased to 5.46 mg/dL; a second kidney biopsy revealed focal segmental glomerular sclerosis and marked tubulointerstitial fibrosis. She was started on hemodialysis.LessonsWe describe a patient with a metastatic melanoma who developed progressive kidney failure during treatment with dabrafenib and trametinib. The most prominent microscopy findings were glomerular endothelial damage in the initial kidney biopsy and accelerated glomerular sclerosis and tubulointerstitial fibrosis in the follow-up biopsy. We hypothesize that a decreased renal reserve and impairment of kidney repair capacity caused by inhibition of B-RAF, a downstream mediator of vascular endothelial growth factor, may explain the progressive kidney injury.Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc.

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