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Published on: January 7, 2015
Nephrotoxicity From Molecularly Targeted Chemotherapeutic Agents
Jaya Kala1, Liann Abu Salman2, Abdallah S Geara2
1Department of Internal Medicine, University of Texas Health Science Center-McGovern Medical School, Houston, TX; Department of Emergency Medicine, University of Texas- MD Anderson Cancer Center, Houston, TX.
Abstract:
The introduction of novel molecularly targeted therapies in the last 2 decades has significantly improved the patient survival compared to standard conventional chemotherapies. However, this improvement has been accompanied by a whole new spectrum of kidney adverse events. Although known as "targeted," many of these agents lack specificity and selectivity, and they have a tendency to inhibit multiple targets including those in the kidneys. Early detection and correct management of kidney toxicities is crucial to preserve kidney functions. The knowledge of these toxicities helps guide optimal and continued utilization of these potent therapies. The incidence, severity, and pattern of nephrotoxicity may vary depending on the respective target of the drug. Here, we review the mechanism of action, clinical findings of kidney adverse events, and their proposed management strategies.
Insights
Novel targeted cancer therapies improve survival but can cause kidney adverse events. Early detection and management of these kidney toxicities are crucial for preserving kidney function and optimizing treatment.
Area of Science:
- Oncology
- Nephrology
- Pharmacology
Background:
- Molecularly targeted therapies have advanced cancer treatment, improving patient survival over conventional chemotherapy.
- These novel therapies can cause a range of kidney adverse events due to off-target effects.
- Understanding and managing these nephrotoxicities is vital for sustained therapeutic use.
Purpose of the Study:
- To review the mechanisms of action of novel targeted therapies.
- To describe the clinical findings associated with kidney adverse events.
- To outline proposed management strategies for drug-induced kidney toxicities.
Main Methods:
- Literature review of molecularly targeted therapies and their associated nephrotoxicities.
- Analysis of mechanisms of action, clinical presentations, and management approaches.
- Synthesis of current knowledge on kidney adverse events from targeted agents.
Main Results:
- Targeted therapies, despite their name, often lack specificity, leading to kidney damage.
- Nephrotoxicity patterns vary based on the drug's specific molecular target.
- Effective management strategies are essential for continuing potent cancer treatments.
Conclusions:
- Kidney adverse events are a significant concern with novel targeted therapies.
- Prompt identification and management of nephrotoxicity are key to preserving renal function.
- Further research into targeted therapy-induced kidney toxicities is warranted.
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