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Updated: Aug 6, 2026

Chemotherapy-induced Vascular Toxicity - Real-time In vivo Imaging of Vessel Impairment
Published on: January 7, 2015
[Anticancer drug-induced nephrotoxicity]
Corinne Isnard-Bagnis1, Bruno Moulin, Vincent Launay-Vacher
1Service de Néphrologie, Hôpital Pitié-Salpêtrière, 83, Boulevard de l'Hôpital, 75013 Paris, France. corinne.bagnis@psl.ap-hop-paris.fr
Abstract:
Nephrotoxicity is an inherent adverse effect of certain anticancer drugs. Anti neoplasic drugs have a narrow therapeutic index and the amount of drug necessary to produce a significant reduction in tumour burden usually produces significant nephrotoxicity. The dosage used in clinical trials represents often the maximum tolerated doses determined during phase I drug evaluation. Greater toxicity is acceptable during curative therapy than during palliative therapy. But cancer patients often exhibit excretory reduced organ function. Modulation of pharmacokinetics and pharmacodynamics of these drugs in cancer patients is therefore necessary in order to improve tolerance. Patients with malignancies are particularly vulnerable to development of renal abnormalities. Conversely, patients with renal abnormalities who have undergone kidney transplantation are at high risk for malignancy. Clinical syndromes of renal involvement are diverse and sometimes insidious. Despite the recent advances in understanding the mechanism of anticancer drug nephrotoxicity, prevention still relies on drug dosage decrease and active screening for renal abnormalities as part of the usual biological work up in patients treated with anticancer drugs.
Insights
Anticancer drugs can cause kidney damage (nephrotoxicity) due to their narrow therapeutic index. Managing drug doses and monitoring kidney function are crucial for cancer patients undergoing treatment.
Area of Science:
- Oncology
- Nephrology
- Pharmacology
Context:
- Anticancer drugs, particularly those with a narrow therapeutic index, frequently cause nephrotoxicity.
- Cancer patients often have pre-existing or treatment-induced renal impairment, increasing vulnerability.
- A bidirectional relationship exists: malignancies increase renal risk, and renal disease increases malignancy risk, especially post-transplant.
Purpose:
- To highlight the inherent nephrotoxicity of anticancer agents.
- To emphasize the challenges in managing drug dosages in cancer patients with compromised renal function.
- To underscore the need for pharmacokinetic and pharmacodynamic modulation of these drugs.
Summary:
- Nephrotoxicity is a significant adverse effect of anticancer drugs, often dose-limiting.
- Cancer patients' compromised renal function complicates treatment, necessitating careful drug management.
- Current prevention strategies include dose reduction and vigilant renal screening.
Impact:
- Improved understanding of anticancer drug nephrotoxicity mechanisms.
- Potential for optimized therapeutic strategies to enhance drug tolerance in cancer patients.
- Enhanced patient outcomes through better management of renal function during cancer therapy.
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