Ifosfamide nephrotoxicity in adult patients

Author:

Ensergueix Gaël1ORCID,Pallet Nicolas1,Joly Dominique2,Levi Charlène1,Chauvet Sophie1,Trivin Claire1,Augusto Jean-Francois3ORCID,Boudet Rémi4,Aboudagga Hail5,Touchard Guy6,Nochy Dominique7,Essig Marie8,Thervet Eric1,Lazareth Hélène1,Karras Alexandre1

Affiliation:

1. Department of Nephrology, Dialysis, Transplantation, Georges Pompidou European Hospital, Paris, France

2. Department of Nephrology, Dialysis, Necker Hospital, Paris, France

3. Department of Nephrology, Dialysis, Transplantation, Angers University Hospital, Paris, France

4. Department of Nephrology, Dialysis, Brive-La-Gaillarde General Hospital, Paris, France

5. Department of Pharmacology, Georges Pompidou European Hospital, Paris, France

6. Department of Nephrology, Dialysis, Transplantation, Poitiers University Hospital, Paris, France

7. Department of Anatomopathology, Georges Pompidou European Hospital, Paris, France

8. Department of Nephrology, Dialysis, Transplantation, Limoges University Hospital, Paris, France

Abstract

Abstract Background Ifosfamide, a widely prescribed antineoplasic agent, is frequently associated with kidney dysfunction. Its nephrotoxicity is well documented in children, but data are lacking in adult patients. Methods The aim of this retrospective study was to describe the clinical, biological and histological characteristics of ifosfamide nephrotoxicity. Results We report 34 patients (median age: 41 years) admitted in six French nephrology departments for kidney failure and/or tubular dysfunction. Fifteen patients (44.1%) received cisplatin as part of their chemotherapy. In 6 patients (17.7%), ifosfamide nephrotoxicity was revealed by a proximal tubular dysfunction (PTD), in 5 patients (14.4%) by an acute kidney injury (AKI), in 6 patients (17.7%) by a chronic kidney disease (CKD) and in 17 patients (49.7%) by an association of PTD and AKI. Fourteen renal biopsies (41.2%) were performed and revealed acute tubular necrosis (85.7%), vacuolation (78.6%) and nuclear atypias (71.4%) of renal epithelial cells, interstitial inflammation (71.4%) and fibrosis (57.1%). Electron microscopy showed mitochondrial enlargement and dysmorphic changes suggestive of mitochondrial toxicity. Ten patients (29.4%) progressed to Stage 5 CKD, six (17.6%) required haemodialysis and six patients died during a median follow-up period of 31 months. Risk factors for Stage 5 CKD were age and cisplatin co-administration.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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