Related Experiment Video
Updated: May 23, 2026
![Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F62334.jpg&w=3840&q=50)
Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
Published on: February 17, 2022
Neurotoxicity of biologically targeted agents in pediatric cancer trials
Elizabeth M Wells1, Amulya A Nageswara Rao, Joseph Scafidi
1Brain Tumor Institute, Children's National Medical Center, Washington, DC, USA.
Abstract:
Biologically targeted agents offer the promise of delivering specific anticancer effects while limiting damage to healthy tissue, including the central and peripheral nervous systems. During the past 5-10 years, these agents were examined in preclinical and adult clinical trials, and are used with increasing frequency in children with cancer. This review evaluates current knowledge about neurotoxicity from biologically targeted anticancer agents, particularly those in pediatric clinical trials. For each drug, neurotoxicity data are reviewed in adult (particularly studies of brain tumors) and pediatric studies when available. Overall, these agents are well tolerated, with few serious neurotoxic effects. Data from younger patients are limited, and more neurotoxicity may occur in the pediatric population because these agents target pathways that control not only tumorigenesis but also neural maturation. Further investigation is needed into long-term neurologic effects, particularly in children.
Insights
Biologically targeted anticancer agents show low neurotoxicity in adults and children. However, limited pediatric data necessitates further study on long-term neurologic effects in children undergoing cancer treatment.
Area of Science:
- Oncology
- Neuroscience
- Pharmacology
Background:
- Biologically targeted agents offer precise anticancer effects with reduced healthy tissue damage.
- These agents are increasingly used in pediatric oncology, necessitating neurotoxicity evaluation.
- Previous research focused on adult trials, with limited data on pediatric neurotoxicity.
Purpose of the Study:
- To review current knowledge on neurotoxicity associated with biologically targeted anticancer agents.
- To specifically assess neurotoxicity data from pediatric clinical trials.
- To identify gaps in understanding long-term neurologic effects in children.
Main Methods:
- Systematic review of preclinical and clinical trial data.
- Analysis of neurotoxicity findings in adult studies, especially those involving brain tumors.
- Compilation and assessment of available pediatric neurotoxicity data for targeted agents.
Main Results:
- Biologically targeted agents are generally well-tolerated with minimal serious neurotoxic effects observed.
- Adult studies, including those with brain tumors, provide a baseline for toxicity.
- Pediatric data are limited, suggesting potential for increased neurotoxicity in this population.
Conclusions:
- Biologically targeted agents are largely safe, but neurotoxicity requires careful monitoring in pediatric cancer patients.
- The targeting pathways involved in both tumorigenesis and neural maturation may increase pediatric neurotoxicity risk.
- Further research is crucial to understand and manage long-term neurologic sequelae in children treated with these novel agents.
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Drug Toxicity: Dose-Dependent Reactions
Pharmacokinetics in Pediatric Patients: Drug Excretion
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Pharmacokinetics in Pediatric Patients: Drug Distribution
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
