The Association between Clinician-Based Common Terminology Criteria for Adverse Events (CTCAE) and Patient-Reported Outcomes (PRO): A Systematic Review

PURPOSE: Symptomatic adverse events (AEs) are monitored by clinicians as part of all US-based clinical trials in cancer via the U.S. National Cancer Institute’s Common Terminology Criteria for Adverse Events (CTCAE) for the purposes of ensuring patient safety. Recently there has been a charge toward...

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Detalhes bibliográficos
Publicado no:Support Care Cancer
Main Authors: Atkinson, Thomas M., Ryan, Sean J., Bennett, Antonia V., Stover, Angela M., Saracino, Rebecca M., Rogak, Lauren J., Jewell, Sarah T., Matsoukas, Konstantina, Li, Yuelin, Basch, Ethan
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4919215/
https://ncbi.nlm.nih.gov/pubmed/27260018
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00520-016-3297-9
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