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Updated: May 17, 2026

Evaluating the Effectiveness of Cancer Drug Sensitization In Vitro and In Vivo
Published on: February 6, 2015
Practical guidelines for dose individualization of anticancer targeted drugs
María Isabel Sáez1, Cristina Quero, José Manuel Trigo
1Department of Medical Oncology, Hospital Universitario Virgen de la Victoria, Campus Universitario Teatinos s/n, 29010, Málaga, Spain. msaez.med@gmail.com
Minimizing variability in anticancer drug exposure is crucial for efficacy and safety. This review provides guidelines for adjusting starting doses of targeted anticancer agents based on renal and liver function.
Area of Science:
- Oncology
- Pharmacology
- Nephrology
- Hepatology
Background:
- Anticancer agents require dose individualization to manage toxicity and optimize therapeutic benefit.
- Renal and hepatic function significantly impact the elimination of many anticancer drugs.
- Optimal starting doses for antineoplastic agents in patients with organ dysfunction are not well-established.
Purpose of the Study:
- To review trials assessing dosing strategies for new targeted anticancer agents in patients with renal or hepatic dysfunction.
- To provide practical guidelines for dose individualization of monoclonal antibodies and tyrosine kinase inhibitors.
Main Methods:
- Literature review of clinical trials evaluating targeted anticancer agents.
- Analysis of dosing strategies in patients with overt biochemical renal and liver dysfunction.
Main Results:
- Discusses specific dosing strategies for targeted agents like monoclonal antibodies and tyrosine kinase inhibitors.
- Highlights the importance of considering renal and liver function for safe and effective dosing.
Conclusions:
- Dose individualization based on renal and liver function is essential for targeted anticancer therapies.
- Recommendations and practical guidelines are provided for clinicians to manage dosing in patients with organ dysfunction.
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