Bevacizumab-Induced Thrombotic Microangiopathy (TMA) in Metastatic Lung Adenocarcinoma Patients Receiving Nivolumab Combined with Bevacizumab, Carboplatin and Paclitaxel: Two Case Reports.
Ping-Chih HsuTai-Di ChenTsung-Yu TsaiCheng-Ta YangPublished in: Clinics and practice (2023)
Anti-programmed death-1 (PD-1)/programmed death ligand 1 (PD-L1) immune checkpoint inhibitors (ICIs), combined with bevacizumab and platinum-based chemotherapy, have shown promising efficacy in treating metastatic non-squamous cell lung cancer in phase 3 clinical trials. However, drug-induced nephrotoxicity is an uncommon but threatening adverse effect when using this combination therapy, and should be evaluated and managed carefully. Here, we present two patients experiencing late-onset asymptomatic heavy proteinuria during the clinical trial. Kidney biopsies performed finally identified bevacizumab-induced thrombotic microangiopathy (TMA), and the proteinuria was decreased after discontinuing bevacizumab permanently. Our report suggests that a kidney biopsy is needed for those receiving ICIs in combination with bevacizumab and chemotherapy and experiencing nephrotoxicity such as heavy proteinuria.
Keyphrases
- drug induced
- liver injury
- clinical trial
- metastatic colorectal cancer
- late onset
- combination therapy
- squamous cell carcinoma
- small cell lung cancer
- squamous cell
- newly diagnosed
- early onset
- high glucose
- end stage renal disease
- ejection fraction
- adverse drug
- locally advanced
- diabetic rats
- emergency department
- radiation therapy
- prognostic factors
- case report
- study protocol
- open label
- oxidative stress
- endothelial cells
- double blind
- fine needle aspiration