Development of the National Cancer Institute’s Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

The standard approach for documenting symptomatic adverse events (AEs) in cancer clinical trials involves investigator reporting using the National Cancer Institute’s (NCI’s) Common Terminology Criteria for Adverse Events (CTCAE). Because this approach underdetects symptomatic AEs, the NCI issued tw...

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Detalhes bibliográficos
Main Authors: Basch, Ethan, Reeve, Bryce B., Mitchell, Sandra A., Clauser, Steven B., Minasian, Lori M., Dueck, Amylou C., Mendoza, Tito R., Hay, Jennifer, Atkinson, Thomas M., Abernethy, Amy P., Bruner, Deborah W., Cleeland, Charles S., Sloan, Jeff A., Chilukuri, Ram, Baumgartner, Paul, Denicoff, Andrea, St. Germain, Diane, O’Mara, Ann M., Chen, Alice, Kelaghan, Joseph, Bennett, Antonia V., Sit, Laura, Rogak, Lauren, Barz, Allison, Paul, Diane B., Schrag, Deborah
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2014
Assuntos:
Commentary
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4200059/
https://ncbi.nlm.nih.gov/pubmed/25265940
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jnci/dju244
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