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A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Toxicity Management of Systemic Kidney Cancer Therapies
Qian Qin1, Ellen Nein2, Andrea Flaten1
1Division of Hematology and Oncology, Department of Internal Medicine, UT Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-8852, USA; Harold C. Simmons Comprehensive Cancer Center.
Abstract:
Systemic treatments for metastatic renal cell carcinoma have expanded to include antiangiogenic agents targeting either vascular endothelial growth factor receptor, immune checkpoint inhibitors against cytotoxic T-lymphocyte antigen 4, or programmed cell death 1 pathways, and combinations of these treatments. The hypoxia inducible factor-2 inhibitors are emerging, whereas mammalian target of rapamycin (inhibitors) role is fading. To sustain optimal efficacy of these agents, potential toxicities must be recognized early and clinically managed. Here, the authors discuss the adverse events attributable to these treatments and management strategies.
Insights
New systemic treatments for metastatic renal cell carcinoma, including antiangiogenic agents and immune checkpoint inhibitors, require early recognition and management of potential toxicities for optimal patient outcomes.
Area of Science:
- Oncology
- Pharmacology
Background:
- Systemic treatments for metastatic renal cell carcinoma (mRCC) have evolved significantly.
- Current therapies include antiangiogenic agents, immune checkpoint inhibitors (ICIs), and their combinations.
Purpose of the Study:
- To review the adverse events associated with modern systemic therapies for mRCC.
- To provide guidance on the clinical management of these treatment-related toxicities.
Main Methods:
- Literature review of systemic treatments for mRCC.
- Discussion of adverse event profiles for targeted therapies and ICIs.
- Synthesis of management strategies for identified toxicities.
Main Results:
- Antiangiogenic agents targeting vascular endothelial growth factor receptor (VEGFR) have specific toxicity profiles.
- Immune checkpoint inhibitors targeting cytotoxic T-lymphocyte antigen 4 (CTLA-4) and programmed cell death 1 (PD-1) pathways can cause immune-related adverse events.
- Emerging hypoxia-inducible factor-2 (HIF-2) inhibitors represent a new class of agents.
Conclusions:
- Early identification and proactive management of adverse events are crucial for maintaining treatment efficacy in mRCC.
- Understanding the specific toxicities of different drug classes allows for tailored clinical interventions.
- Ongoing research focuses on novel agents and optimizing treatment strategies for mRCC.
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