Feasibility of Patient Reporting of Symptomatic Adverse Events via the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) in a Chemoradiotherapy Cooperative Group Multicenter Clinical Trial

Ethan Basch(UNC Lineberger Comprehensive Cancer Center), Stephanie L. Pugh(NRG Oncology), Amylou C. Dueck(Mayo Clinic in Arizona), Sandra A. Mitchell(National Cancer Institute), Lawrence Berk(University of South Florida), Shannon Fogh(University of California, San Francisco), Lauren J. Rogak(Memorial Sloan Kettering Cancer Center), Marcha L. Gatewood(Emory University), Bryce B. Reeve(University of North Carolina at Chapel Hill), Tito R. Mendoza(The University of Texas MD Anderson Cancer Center), Ann M. O’Mara(National Cancer Institute), Andrea Denicoff(National Cancer Institute), Lori M. Minasian(National Cancer Institute), Antonia V. Bennett(University of North Carolina at Chapel Hill), Ann Setser, Deborah Schrag(Dana-Farber Cancer Institute), Kevin S. Roof(Southeast Clinical Oncology Research Consortium), Joan K. Moore, Thomas Gergel(Geisinger Medical Center), Kevin L. Stephans(Cleveland Clinic), Andreas Rimner(Memorial Sloan Kettering Cancer Center), Albert S. DeNittis(Main Line Health), Deborah Watkins Bruner(Emory University)
International Journal of Radiation Oncology*Biology*Physics
February 10, 2017
10.1016/j.ijrobp.2017.02.002
Cited by 119

Abstract

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