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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Détails bibliographiques
Auteurs principaux: 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
Format: Artigo
Langue:Inglês
Publié: Oxford University Press 2014
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Commentary
Accès en ligne: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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