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Acute interstitial nephritis associated with immune checkpoint inhibitors: a single-centre experience

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 even...

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Autores principales: Oleas, Diana, Bolufer, Mónica, Agraz, Irene, Felip, Enriqueta, Muñoz, Eva, Gabaldón, Alejandra, Bury, Roxana, Espinel, Eugenia, Serón, Daniel, García-Carro, Clara, Soler, María José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247740/
https://www.ncbi.nlm.nih.gov/pubmed/34221369
http://dx.doi.org/10.1093/ckj/sfaa008
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author Oleas, Diana
Bolufer, Mónica
Agraz, Irene
Felip, Enriqueta
Muñoz, Eva
Gabaldón, Alejandra
Bury, Roxana
Espinel, Eugenia
Serón, Daniel
García-Carro, Clara
Soler, María José
author_facet Oleas, Diana
Bolufer, Mónica
Agraz, Irene
Felip, Enriqueta
Muñoz, Eva
Gabaldón, Alejandra
Bury, Roxana
Espinel, Eugenia
Serón, Daniel
García-Carro, Clara
Soler, María José
author_sort Oleas, Diana
collection PubMed
description 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.
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spelling pubmed-82477402021-07-02 Acute interstitial nephritis associated with immune checkpoint inhibitors: a single-centre experience Oleas, Diana Bolufer, Mónica Agraz, Irene Felip, Enriqueta Muñoz, Eva Gabaldón, Alejandra Bury, Roxana Espinel, Eugenia Serón, Daniel García-Carro, Clara Soler, María José Clin Kidney J Original Articles 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. Oxford University Press 2020-02-10 /pmc/articles/PMC8247740/ /pubmed/34221369 http://dx.doi.org/10.1093/ckj/sfaa008 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Oleas, Diana
Bolufer, Mónica
Agraz, Irene
Felip, Enriqueta
Muñoz, Eva
Gabaldón, Alejandra
Bury, Roxana
Espinel, Eugenia
Serón, Daniel
García-Carro, Clara
Soler, María José
Acute interstitial nephritis associated with immune checkpoint inhibitors: a single-centre experience
title Acute interstitial nephritis associated with immune checkpoint inhibitors: a single-centre experience
title_full Acute interstitial nephritis associated with immune checkpoint inhibitors: a single-centre experience
title_fullStr Acute interstitial nephritis associated with immune checkpoint inhibitors: a single-centre experience
title_full_unstemmed Acute interstitial nephritis associated with immune checkpoint inhibitors: a single-centre experience
title_short Acute interstitial nephritis associated with immune checkpoint inhibitors: a single-centre experience
title_sort acute interstitial nephritis associated with immune checkpoint inhibitors: a single-centre experience
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247740/
https://www.ncbi.nlm.nih.gov/pubmed/34221369
http://dx.doi.org/10.1093/ckj/sfaa008
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