Incorporating Information From Proxies for Patient-Centered Outcomes in Adult and Pediatric Oncology Settings-Reference-Cited by-同舟云学术

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Incorporating Information From Proxies for Patient-Centered Outcomes in Adult and Pediatric Oncology Settings

Published:2023-03-10 Issue:8 Volume:41 Page:1518-1522
ISSN:0732-183X
Container-title:Journal of Clinical Oncology
language:en
Short-container-title:JCO

Author:

Roydhouse Jessica¹²^ORCID,Reeve Bryce B.³^ORCID

Affiliation:

1. Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia

2. Department of Health Services, Policy and Practice, Brown University School of Public Health, Providence, RI

3. Center for Health Measurement, Department of Population Health Sciences, Duke University School of Medicine, Durham, NC

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

Link

https://ascopubs.org/doi/pdfdirect/10.1200/JCO.22.01049

Reference57 articles.

1. Missing quality of life data in cancer clinical trials: serious problems and challenges

2. International standards for the analysis of quality-of-life and patient-reported outcome endpoints in cancer randomised controlled trials: recommendations of the SISAQOL Consortium

3. Gathering data from older adults via proxy respondents: research challenges

4. Lack of Concordance in Symptomatic Adverse Event Reporting by Children, Clinicians, and Caregivers: Implications for Cancer Clinical Trials

5. Agreement Between Child Self-report and Caregiver-Proxy Report for Symptoms and Functioning of Children Undergoing Cancer Treatment

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