Clinician vs Patient Reporting of Baseline and Postbaseline Symptoms for Adverse Event Assessment in Cancer Clinical Trials-Reference-Cited by-同舟云学术

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Clinician vs Patient Reporting of Baseline and Postbaseline Symptoms for Adverse Event Assessment in Cancer Clinical Trials

Published:2020-03-01 Issue:3 Volume:6 Page:437
ISSN:2374-2437
Container-title:JAMA Oncology
language:en
Short-container-title:JAMA Oncol

Author:

Atkinson Thomas M.¹,Dueck Amylou C.²,Satele Daniel V.³,Thanarajasingam Gita⁴,Lafky Jacqueline M.⁴,Sloan Jeff A.³,Basch Ethan¹⁵

Affiliation:

1. Memorial Sloan Kettering Cancer Center, New York, New York

2. Alliance Statistics and Data Center, Mayo Clinic, Scottsdale, Arizona

3. Alliance Statistics and Data Center, Mayo Clinic, Rochester, Minnesota

4. Mayo Clinic, Rochester, Minnesota

5. University of North Carolina at Chapel Hill, Chapel Hill, North Carolina

Publisher

American Medical Association (AMA)

Subject

Oncology,Cancer Research

Link

https://jamanetwork.com/journals/jamaoncology/articlepdf/2757517/jamaoncology_atkinson_2019_ld_190026.pdf

Reference6 articles.

1. Methods for implementing and reporting patient-reported outcome (PRO) measures of symptomatic adverse events in cancer clinical trials.;Basch;Clin Ther,2016

2. Patient-reported outcomes: an essential component of oncology drug development and regulatory review.;Basch;Lancet Oncol,2018

3. Patient-reported outcomes—harnessing patients’ voices to improve clinical care.;Basch;N Engl J Med,2017

4. Missing patients’ symptoms in cancer care delivery—the importance of patient-reported outcomes.;Basch;JAMA Oncol,2016

5. Note on the sampling error of the difference between correlated proportions or percentages.;McNEMAR;Psychometrika,1947

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