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Nephrotoxicity Associated with Novel Anticancer Agents (Aflibercept, Dasatinib, Nivolumab): Case Series and
Luca Piscitani1, Vittorio Sirolli1, Lorenzo Di Liberato1
1Nephrology and Dialysis Unit, Department of Medicine, G. d'Annunzio University, Chieti-Pescara, SS. Annunziata Hospital, Via dei Vestini, 66013 Chieti, Italy.
Abstract:
Cancer patients have an incidence of about 60% kidney disease development and are at elevated risk of acute renal damage. Kidney disease in these patients is frequently associated with nephrotoxicity from the ongoing oncological treatment. New anticancer therapeutic strategies, such as targeted therapies and immunotherapies, offer substantial benefits in the treatment of many neoplasms. However, their use is associated with significant nephrotoxicity, which qualitatively differs from that seen with traditional cytotoxic chemotherapy, while the underlying mechanisms are complex and still to be clearly defined. Nephrologists need to be knowledgeable about the array of such renal toxicities for effective collaboration with the oncologist in the prevention and management of kidney involvement. Renal adverse effects may range from asymptomatic proteinuria to renal failure, and their prompt identification and timely treatment is essential for optimal and safe care of the patient. In this article, after presenting clinical cases we discuss the differing renal toxicity of three novel anticancer agents (aflibercept, dasatinib, and nivolumab) and possible measures to counter it.
Insights
Cancer patients frequently develop kidney disease due to oncological treatments. This study details the distinct kidney toxicities of novel cancer therapies like aflibercept, dasatinib, and nivolumab, and discusses management strategies.
Area of Science:
- Nephrology
- Oncology
- Pharmacology
Background:
- Cancer patients have a high incidence (60%) of kidney disease, often linked to treatment-induced nephrotoxicity.
- Novel cancer therapies (targeted therapies, immunotherapies) present unique nephrotoxicity profiles distinct from traditional chemotherapy.
- Understanding these complex mechanisms is crucial for nephrologists collaborating with oncologists.
Purpose of the Study:
- To elucidate the specific renal toxicities associated with novel anticancer agents.
- To discuss preventative and management strategies for cancer treatment-related kidney disease.
- To highlight the importance of nephrologist-oncologist collaboration.
Main Methods:
- Clinical case presentations of patients treated with novel anticancer agents.
- Discussion of the differing nephrotoxicity profiles of aflibercept, dasatinib, and nivolumab.
- Review of current understanding of underlying mechanisms and management approaches.
Main Results:
- Novel anticancer agents exhibit unique patterns of renal toxicity, differing from conventional chemotherapy.
- Aflibercept, dasatinib, and nivolumab are associated with specific nephrotoxic effects requiring tailored management.
- Prompt identification and timely intervention are critical for managing renal adverse events.
Conclusions:
- Nephrologists must be aware of the diverse renal toxicities posed by modern cancer treatments.
- Effective management of cancer-related kidney disease necessitates a collaborative approach between oncologists and nephrologists.
- Further research into the mechanisms of novel agent nephrotoxicity is warranted.
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