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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
Duration of targeted therapy for metastatic renal cell carcinoma: a review of current practices
1Centre Léon Bérard, Lyon, France. negrier@lyon.fnclcc.fr
Abstract:
The development of targeted agents has substantially improved clinical outcomes for patients with metastatic renal cell carcinoma. The optimum duration of treatment with these agents is not yet clear, particularly as targeted agents may often result in disease stabilization as well as in tumour response. Some clinicians may choose to switch to an alternative agent in the absence of tumour response or in the event of the occurrence of side effects, which can result in patients moving rapidly through the available treatment options. This review evaluates the duration of treatment observed with targeted agents that are approved for first-line treatment of metastatic renal cell carcinoma and considers the reasons for switching or discontinuing therapy. In addition, practical strategies for achieving optimal treatment duration, through adverse event management, are discussed.
Insights
Determining the optimal duration for targeted therapy in metastatic renal cell carcinoma is crucial. This review examines treatment lengths and reasons for switching therapies, offering strategies for effective adverse event management.
Area of Science:
- Oncology
- Pharmacology
Background:
- Targeted agents have significantly improved outcomes for metastatic renal cell carcinoma (mRCC).
- The ideal duration of targeted therapy for mRCC remains unclear.
- Disease stabilization and tumor response are common with targeted agents.
Purpose of the Study:
- To review treatment durations with first-line targeted agents for mRCC.
- To identify reasons for treatment discontinuation or switching.
- To discuss strategies for optimizing treatment duration via adverse event management.
Main Methods:
- Literature review of targeted agents approved for first-line mRCC treatment.
- Analysis of treatment durations and reasons for therapy changes.
- Discussion of adverse event management strategies.
Main Results:
- Varied treatment durations observed with approved first-line targeted agents.
- Tumor response, disease stabilization, and adverse events influence treatment decisions.
- Rapid progression through treatment options can occur due to switching.
Conclusions:
- Optimal treatment duration for targeted agents in mRCC requires further investigation.
- Effective adverse event management is key to achieving optimal treatment duration.
- Strategies for managing side effects can help prolong therapy and improve patient outcomes.
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