| Literature DB >> 36180718 |
Daisuke Morita1, Kenji Ito2, Nobumitsu Ikeuchi3, Yoshihiro Nishida1, Fumiyasu Igata3, Tsubasa Nakamura1, Hiroyuki Murayama1, Maho Watanabe1, Koji Takahashi1, Tetsuhiko Yasuno1, Noriko Uesugi4, Masaki Fujita3, Takashi Oda5, Kosuke Masutani1.
Abstract
Afatinib is a second-generation, oral, epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI). One of the most common adverse effects of affatinib is diarrhea, which may lead to acute kidney injury (AKI) due to severe plasma volume loss; however, no case of glomerular injury directly induced by afatinib has been reported to date. Here, we describe the case of a 53-year-old Japanese male patient with advanced lung adenocarcinoma who twice developed AKI requiring dialysis, once after starting and once after increasing the dose of afatinib. Although serum anti-neutrophil cytoplasmic antibodies were negative, crescentic glomerulonephritis with no immune deposits was confirmed on kidney biopsy. No vasculitis-like signs were observed in other organs, such as lung, skin, or peripheral nerves. Afatinib was considered the cause of glomerular damage and was immediately discontinued; corticosteroids were administered. Renal function gradually recovered thereafter, with serum creatinine levels at ~ 2.3 mg/dL after second-line therapy with bevacizumab and atezolizumab. Several cases of cutaneous leukocytoclastic vasculitis have been reported in patients treated with other EGFR-TKIs; therefore, afatinib-induced vasculitis may lead to crescentic glomerulonephritis. Although afatinib-induced glomerular injury is extremely rare and has an unclear mechanism, renal function and urinary findings need to be closely monitored.Entities:
Keywords: Afatinib; Epidermal growth factor receptor-tyrosine kinase inhibitor; Glomerulonephritis; Renal function
Year: 2022 PMID: 36180718 DOI: 10.1007/s13730-022-00737-8
Source DB: PubMed Journal: CEN Case Rep ISSN: 2192-4449