Incorporating Information From Proxies for Patient-Centered Outcomes in Adult and Pediatric Oncology Settings
- 10 March 2023
- journal article
- editorial
- Published by American Society of Clinical Oncology (ASCO) in Journal of Clinical Oncology
- Vol. 41 (8) , 1518-1522
Abstract
Priorities for proxy research to advance patient-centered outcome data collection in oncologyKeywords
This publication has 49 references indexed in Scilit:
- Effectiveness of a Web-Based Application to Monitor Health-Related Quality of LifePediatrics, 2013
- Agreement between pediatric brain tumor patients and parent proxy reports regarding the Pediatric Functional Assessment of Cancer Therapy–Childhood Brain Tumor Survivors questionnaire, version 2Cancer, 2010
- Semiparametric regression models for repeated measures of mortal cohorts with non‐monotone missing outcomes and time‐dependent covariatesStatistics in Medicine, 2010
- Detecting, measuring, and testing dyadic patterns in the actor–partner interdependence model.Journal of Family Psychology, 2010
- Adverse Symptom Event Reporting by Patients vs Clinicians: Relationships With Clinical OutcomesJNCI: Journal of the National Cancer Institute, 2009
- How Do Proxy Responses and Proxy‐Assisted Responses Differ from What Medicare Beneficiaries Might Have Reported about Their Health Care?Health Services Research, 2008
- Assessment of health‐related quality of life in children with cancerCancer, 2006
- Agreement between child self-report and parent proxy-report to evaluate Quality of Life in Children with CancerPsycho-Oncology, 2005
- Three Instruments to Assess Fatigue in Children with CancerJournal of Pain and Symptom Management, 2003
- Patients With Cancer and Next-of-Kin Response Comparability on Physical and Psychological Symptom Well-beingCancer Nursing, 2002