Acute interstitial nephritis associated with immune checkpoint inhibitors: a single-centre experience
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Published on: May 6, 2018
Diana Oleas1, Mónica Bolufer1, Irene Agraz1
1Department of Nephrology, Vall d'Hebron University Hospital, Barcelona, Spain.
Background:
Checkpoint inhibitors (CPIs) are used to treat solid organ metastatic malignancies. They act by triggering a vigorous immune response against tumoural cells, preventing their proliferation and metastasis. However, this is not a selective response and can cause immune-related adverse events (irAEs). The kidney can potentially be damaged, with an incidence of irAEs of 1-4%. The most frequent type of toxicity described is acute interstitial nephritis (AIN).
Methods:
We conducted a study of patients with solid organ metastatic malignancies treated with immunotherapy who developed acute renal injury and underwent kidney biopsy in the last 14 months at the Vall d'Hebron University Hospital.
Results:
In all, 826 solid organ malignancies were treated with immunotherapy in our centre, 125 of them (15.1%) developed acute kidney injury (AKI), 23 (18.4% of AKI) visited the nephrology department and 8 underwent kidney biopsy. The most frequent malignancy was lung cancer, in five patients (62%), followed by two patients (25%) with melanoma and one patient (12%) with pancreatic cancer. Four patients (50%) had already received previous oncological therapy, and for the remaining four patients (50%), CPI was the first-line therapy. Five patients (62%) were treated with anti-programmed cell death protein 1, three patients (37%) received anti-programmed death ligand 1 and two (25%) patients were treated in combination with anti-cytotoxic T-lymphocyte antigen 4. The time between the start of CPI and the onset of the AKI ranged from 2 to 11 months. The most frequent urine findings were subnephrotic-range proteinuria, with a mean protein:creatinine ratio of 544 mg/g (standard deviation 147) and eosinophiluria. All patients were biopsied after being diagnosed with AIN. Three patients (37%) received treatment with pulses of methylprednisolone 250-500 mg/day and five patients (62%) received prednisone 1 mg/kg/day. Seven patients (87%) experienced recovery of kidney function and one patient (12%) progressed to chronic kidney disease.
Conclusions:
We report on eight patients with CPI-related AIN diagnosed in the last 14 months at our centre. The novel immunotherapy treatment of metastatic solid organ malignancies carries a higher risk of irAEs. The kidney is one of the most commonly affected organs, frequently presenting as an AIN and exhibiting a favourable response to steroid treatment.
Insights
Checkpoint inhibitors (CPIs) can cause kidney damage, specifically acute interstitial nephritis (AIN). Early diagnosis and steroid treatment led to kidney function recovery in most patients with CPI-related AIN.
Area of Science:
- Oncology
- Nephrology
- Immunology
Background:
- Checkpoint inhibitors (CPIs) treat metastatic cancers by boosting immune response.
- CPIs can cause immune-related adverse events (irAEs), including kidney damage (1-4% incidence).
- Acute interstitial nephritis (AIN) is the most common form of CPI-induced kidney toxicity.
Purpose of the Study:
- To investigate the clinical characteristics and outcomes of patients with CPI-related acute kidney injury (AKI).
- To analyze kidney biopsy findings and treatment responses in patients with suspected CPI-induced AIN.
Main Methods:
- Retrospective study of patients with metastatic solid organ malignancies treated with immunotherapy.
- Analysis of patients who developed AKI, underwent nephrology consultation, and kidney biopsy.
- Review of clinical data, including malignancy type, prior therapies, CPI used, and renal outcomes.
Main Results:
- Eight patients with CPI-related AIN were identified from 826 treated malignancies.
- Lung cancer was the most frequent malignancy (62%), followed by melanoma (25%).
- Most patients presented with subnephrotic proteinuria and eosinophiluria; 87% recovered kidney function with steroid treatment.
Conclusions:
- CPI therapy for metastatic cancers is associated with a risk of AIN.
- Kidney involvement as AIN is a significant irAE of CPIs.
- Prompt diagnosis and steroid treatment of CPI-related AIN generally lead to favorable renal outcomes.
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