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Patient Reported Outcomes Version of CTCAE

Known as: PRO-CTCAE, Patient-Reported Outcomes version of the CTCAE (PRO-CTCAE) 
A library of items for patient self-reporting of symptoms and side effects associated with cancer treatment trials.(PRO-CTCAE)
National Institutes of Health

Papers overview

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Highly Cited
2018
Highly Cited
2018
BackgroundThe Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) was developed… Expand
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2018
2018
Purpose The US National Cancer Institute (NCI) Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse… Expand
Review
2017
Review
2017
BackgroundThe US National Cancer Institute (NCI) has developed the Patient-Reported Outcomes version of the Common Terminology… Expand
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2017
2017
PURPOSE To assess the feasibility of measuring symptomatic adverse events (AEs) in a multicenter clinical trial using the… Expand
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2017
2017
Adverse event (AE) reporting in oncology trials is required, but current practice does not directly integrate the child's voice… Expand
Review
2016
Review
2016
Systematic capture of the patient perspective can inform the development of new cancer therapies. Patient-reported outcomes (PROs… Expand
Highly Cited
2015
Highly Cited
2015
IMPORTANCE To integrate the patient perspective into adverse event reporting, the National Cancer Institute developed a patient… Expand
Highly Cited
2015
Highly Cited
2015
PURPOSE To perform a prospective, multi-institutional, phase 2 study of a substantial decrease in concurrent chemoradiation… Expand
Highly Cited
2015
Highly Cited
2015
  • B. Movsas
  • JAMA oncology
  • 2015
  • Corpus ID: 205126718
For more than 30 years, the standard process for reporting toxicities in clinical oncology trials has been via the National… Expand
Highly Cited
2013
Highly Cited
2013
PurposeThe National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events… Expand
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