Childhood Cancer Survivors' Quality of Life
As survival rates for childhood cancers have risen sharply over the past few decades, researchers have turned increasing attention to what life actually looks like for those who make it through treatment. Scientists studying health-related quality of life in pediatric cancer survivors examine physical, emotional, social, and cognitive functioning — often using structured tools like the Pediatric Quality of Life Inventory and drawing on large cohort data from initiatives such as the Childhood Cancer Survivor Study to track outcomes across years and decades. A persistent challenge is reconciling how children, adolescents, parents, and clinicians each perceive the same patient's wellbeing, since parent-proxy reports and self-reports frequently diverge in meaningful ways. Open questions include how to better support the transition of young adult survivors into long-term follow-up care, and how early psychosocial and neurocognitive deficits — common after certain treatments — can be identified and addressed before they compound into lasting disadvantage.
- Works
- 83,387
- Total citations
- 943,166
- Keywords
- Pediatric Quality of Life InventoryChildhood Cancer Survivor StudyHealth-related Quality of LifePediatric Palliative CareAdolescent and Young Adult OncologyPsychosocial Outcomes
Top papers in Childhood Cancer Survivors' Quality of Life
Ordered by total citation count.
- Cochrane Handbook for Systematic Reviews of Interventions↗ 14,668OA
- CBTRUS Statistical Report: Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2006-2010↗ 12,105OA
- The Brief Psychiatric Rating Scale↗ 10,960
- Prevalence of Overweight and Obesity in the United States, 1999-2004↗ 8,758
- Motivational interviewing: preparing people for change.↗ 7,055
- Cochrane Handbook for Systematic Reviews of Interventions↗ 5,854
- Distinguishing optimism from neuroticism (and trait anxiety, self-mastery, and self-esteem): A reevaluation of the Life Orientation Test.↗ 5,731
- Cochrane Handbook for Systematic Reviews of Interventions Version 5.0.1. The Cochrane Collaboration↗ 5,563
- Optimism, coping, and health: Assessment and implications of generalized outcome expectancies.↗ 5,197
- The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005–2008↗ 5,167OA
- PedsQL™ 4.0: Reliability and Validity of the Pediatric Quality of Life Inventory™ Version 4.0 Generic Core Scales in Healthy and Patient Populations↗ 5,131
- Prevalence and Trends in Overweight Among US Children and Adolescents, 1999-2000↗ 4,098
Active researchers
Top authors in this area, ranked by h-index.