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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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Главные авторы: 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
Формат: Artigo
Язык:Inglês
Опубликовано: Oxford University Press 2014
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Online-ссылка: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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