Validation of the German patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE™)

Author:

Hagelstein V.,Ortland I.,Wilmer A.,Mitchell S.A.,Jaehde U.

Publisher

Elsevier BV

Subject

Oncology,Hematology

Reference21 articles.

1. Use of patient-reported outcomes to improve the predictive accuracy of clinician-reported adverse events;Basch;J Natl Cancer Inst,2011

2. Patient-reported outcomes in drug safety evaluation;Basch;Ann Oncol,2009

3. Patient-reported outcomes and the evolution of adverse event reporting in oncology;Trotti;J Clin Oncol,2007

4. Division of Cancer Control and Population Sciences, National Cancer Institute. Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE™). http://healthcaredelivery.cancer.gov/pro-ctcae/ (10 April 2016, date last accessed).

5. Validity and Reliability of the US National Cancer Institute's Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE);Dueck;JAMA Oncol,2015

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