Cited by 67Chemotherapy-induced organ toxicity mitigationAcute Kidney Injury ResearchChildhood Cancer Survivors' Quality of Life

Late renal toxicity of treatment for childhood malignancy: risk factors, long-term outcomes, and surveillance

Open access
Skinner, Roderick·2018·Pediatric Nephrology

Abstract

Chronic glomerular and tubular nephrotoxicity is reported in 20-50% and 20-25%, respectively, of children and adolescents treated with ifosfamide and 60-80% and 10-30%, respectively, of those given cisplatin. Up to 20% of children display evidence of chronic glomerular damage after unilateral nephrectomy for a renal tumour. Overall, childhood cancer survivors have a ninefold higher risk of developing renal failure compared with their siblings. Such chronic nephrotoxicity may have multiple causes, including chemotherapy, radiotherapy exposure to kidneys, renal surgery, supportive care drugs and tumour-related factors. These cause a wide range of chronic glomerular and tubular toxicities, often with potentially severe clinical sequelae. Many risk factors for developing nephrotoxicity, mostly patient and treatment related, have been described, but we remain unable to predict all episodes of renal damage. This implies that other factors may be involved, such as genetic polymorphisms influencing drug metabolism. Although our knowledge of the long-term outcomes of chronic nephrotoxicity is increasing, there is still much to learn, including how we can optimally predict or achieve early detection of nephrotoxicity. Greater understanding of the pathogenesis of nephrotoxicity is needed before its occurrence can be prevented.

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  • The renal glomerulus might be affected by cisplatin treatment in 60-80% of children and adolescents, and renal tubular function is affected by ifosfamide treatment in 20-25%.

    “The renal glomerulus might be affected by cisplatin treatment in 60-80% of children and adolescents and renal tubular function is affected by ifosfamide treatment in 20-25% 171 .”

    From Osteosarcoma (2022) · cites this paper as [171]

  • Cisplatin-induced glomerular effects are rarely severe enough to require treatment, but ifosfamide-induced renal tubular effects can lead to clinically relevant electrolyte wasting in the form of Fanconi syndrome.

    “Cisplatin-induced glomerular effects are rarely severe enough to require treatment but ifosfamide-induced renal tubular effects can lead to clinically relevant electrolyte wasting in the form of Fanconi syndrome 171 .”

    From Osteosarcoma (2022) · cites this paper as [171]

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Authors
Skinner, R.
Affiliations
Great North Children's Hospital (GB)
Corresponding author
Skinner, Roderick
Venue
Pediatric Nephrology
Published
2017-04-22
Volume
33
Issue
2
Pages
215-225
ISSN
  • 0931-041X (ISSN-L)
  • 1432-198X
OpenAlex
W2607407223
Cited by
67
References
76
Citations by year
2026: 6 · 2025: 6 · 2024: 6 · 2023: 10 · 2022: 15 · 2021: 8 · 2020: 5 · 2019: 7 · 2018: 3 · 2017: 1
FWCI
0.70
Type
journal article
Language
en
Open access
Locations
  • Pediatric Nephrology (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Newcastle University ePrints (Newcastle Univesity) (cc-by)
Funders
Newcastle University
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Chemotherapy-induced organ toxicity mitigation
  • Health Sciences › Medicine › Nephrology › Acute Kidney Injury Research
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Childhood Cancer Survivors' Quality of Life
Keywords
childhood cancer survivors, nephrotoxicity, ifosfamide, cisplatin, renal failure, risk factors, long-term outcomes, chemotherapy
MeSH terms
Antineoplastic Agents, Child, Cisplatin, Humans, Ifosfamide, Kidney, Kidney Diseases, Neoplasms, Risk Factors, Time Factors, Carboplatin, Survivors

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