Sunitinib-Induced Acute Interstitial Nephritis in a Thrombocytopenic Renal Cell Cancer Patient
Author(s) -
Ibrahim Azar,
Saghi Esfandiarifard,
Pedram Sinai,
Ali Wazir,
Llewellyn Foulke,
Syed Mehdi
Publication year - 2017
Publication title -
case reports in oncological medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.173
H-Index - 7
eISSN - 2090-6714
pISSN - 2090-6706
DOI - 10.1155/2017/6328204
Subject(s) - sunitinib , medicine , thrombotic microangiopathy , sorafenib , renal biopsy , tyrosine kinase inhibitor , renal cell carcinoma , focal segmental glomerulosclerosis , bevacizumab , acute kidney injury , renal function , vascular endothelial growth factor , proteinuria , adverse effect , cancer , gastroenterology , urology , kidney , hepatocellular carcinoma , vegf receptors , chemotherapy , disease
Sunitinib, a multitargeted tyrosine kinase inhibitor (TKI), is currently the standard of care for patients with metastatic renal cell carcinoma. Renal adverse events associated with sunitinib include proteinuria, renal insufficiency secondary to focal segmental glomerulosclerosis (FSGS), and thrombotic microangiopathy. We describe the second reported instance of biopsy-proven sunitinib-induced acute interstitial nephritis (AIN), in a challenging case complicated by thrombocytopenia. The case illustrates the importance of early diagnosis and intervention in ensuring long-term recovery from renal complications. Four other cases of AIN reported along with inhibition of the vascular endothelial growth factor (VEGF) by either TKI (sunitinib and sorafenib) or antibodies (bevacizumab) suggest a possible class effect. Given our experience, we recommend monitoring renal function with VEGF inhibition, and in the case of renal failure in the setting of an unclear diagnosis, we recommend prompt biopsy.
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