A New Measure of Child-Reported Symptomatic Toxicities of Cancer Treatment: Introducing Pediatric PRO-CTCAE®
Purpose
NCI’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE®) was developed to capture symptomatic toxicity by patient self-report in cancer clinical trials. A pediatric version of PRO-CTCAE (Ped-PRO-CTCAE®) is now available to enable self-reporting of symptomatic adverse events by children and adolescents.
In this webinar speakers and discussants
- Describe the design and psychometric testing of Ped-PRO-CTCAE®
- Demonstrate the creation of customized PRO-CTCAE® surveys
- Highlight the value of this new measure for pediatric oncology trials
Intended Audience
Extramural investigators at junior, mid, and senior levels.
Suggested Readings
- Kluetz PG, Chingos DT, Basch EM, Mitchell SA. Am Soc Clin Oncol Educ Book 2016;35:67-73. doi: 10.14694/EDBK_159514
- Reeve BB et al. Pediatr Blood and Cancer 2017;64(3):1-7. DOI: 10.1002/pbc.26261.
- Reeve BB et al. JNCI. Published online first. https://doi.org/10.1093/jnci/djaa016
Presenters
Pamela S. Hinds, PhD, RN, FAAN
Children's National Hospital
Molly McFatrich, MPH
Duke University School of Medicine
Bryce B. Reeve, PhD
Duke University School of Medicine
Discussants
David R. Freyer, DO, MS
Children's Hospital Los Angeles
USC Norris Comprehensive Cancer Center
Gregory H. Reaman, MD
U.S. Food & Drug Administration
Douglas S. Hawkins, MD
Seattle Children's Hospital
Moderator
Sandra A. Mitchell, PhD, CRNP, FAAN
National Cancer Institute
This webinar will be archived on the HDRP Events webpage.