Publication

Barriers and facilitators of risk-based health care for adult survivors of childhood cancer: A report from the Childhood Cancer Survivor Study

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Last modified
  • 05/21/2025
Type of Material
Authors
    Jennifer S. Ford, City University of New YorkEmily S. Tonorezos, Memorial Sloan Kettering Cancer CenterAnn Mertens, Emory UniversityMelissa M. Hudson, St Jude Childrens Research HospitalJacqueline Casillas, University of California Los AngelesBarbara M. Foster, American Board of Obstetrics & GynecologyChaya S. Moskowitz, Memorial Sloan Kettering Cancer CenterStephanie M. Smith, Stanford UniversityJoanne F. Chou, Memorial Sloan Kettering Cancer CenterGeorge Buchanan, University of Texas Southwestern Medical CenterLeslie L. Robison, St Jude Childrens Research HospitalKevin C. Oeffinger, Duke University
Language
  • English
Date
  • 2019-10-18
Publisher
  • Wiley
Publication Version
Copyright Statement
  • © 2019 American Cancer Society.
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 126
Issue
  • 3
Start Page
  • 619
End Page
  • 627
Grant/Funding Information
  • American Cancer Society Cancer Control Career Development Award #121092.
  • This study was supported by grants from the Robert Wood Johnson Foundation Generalist Physician Faculty Scholar Program (KCO)
  • National Cancer Institute (U24-CA55727, K05-CA165702, CA187397, and P30CA008748)
Abstract
  • Background: Optimal risk-based survivor health care includes surveillance for late effects and education targeted at reducing or preventing risky health behaviors. Understanding the reasons for a lack of risk-based follow-up care is essential. Methods: Adult participants from the Childhood Cancer Survivor Study were surveyed about having a cancer-related visit in the past 2 years and the likelihood of having a cancer-related visit in the future. Additional factors thought to be related to the primary outcomes were also assessed. Results: Nine hundred seventy-five survivors completed the survey. Twenty-seven percent (95% confidence interval [CI], 24%-30%) had a cancer-related medical visit in the previous 2 years, and 41% (95% CI, 38%-44%) planned to have such a visit within the next 2 years. The likelihood of having had a cancer-related visit within the last 2 years was higher among survivors assigning greater importance to these visits (relative risk [RR], 1.2; 95% CI, 1.1-1.3), perceiving greater susceptibility to health problems (RR, 1.2; 95% CI, 1.1-1.3), having a moderate to life-threatening chronic health problem related to their cancer (RR, 2.1; 95% CI, 1.7-2.7), seeing a primary care provider for a cancer-related problem (RR, 1.3; 95% CI, 1.0-1.6), having a cancer treatment summary (RR, 1.3; 95% CI, 1.0-1.6), and endorsing greater confidence in physicians' abilities to address questions and concerns (RR, 1.2; 95% CI, 1.0-1.3). Conclusions: Educational interventions improving awareness of treatment history and susceptibility to cancer-related late effects and corresponding risk-based care are likely to be beneficial for survivors of childhood cancers.
Author Notes
  • Correspondence: Jennifer S. Ford, PhD, Hunter College, Department of Psychology, City University of New York, 695 Park Avenue, HN-611, New York, NY 10065, 212-396-6690 (tel), jennifer.ford@hunter.cuny.edu
Keywords
Research Categories
  • Health Sciences, Human Development
  • Health Sciences, Oncology
  • Health Sciences, Public Health
  • Health Sciences, Health Care Management

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