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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Bibliografski detalji
Glavni autori: 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
Jezik:Inglês
Izdano: Oxford University Press 2014
Teme:
Commentary
Online pristup: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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