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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Bibliographic Details
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
Format: Artigo
Language:Inglês
Published: Oxford University Press 2014
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Commentary
Online Access: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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