Childhood cancer models of survivorship care: a scoping review of elements of care and reported outcomes

Natalie Bradford, Raymond Javan Chan, Xiomara Skrabal Ross, Carla Thamm, Erin Sharwood, Jason Pole, Christine Cashion, Larissa Nekhlyudov

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Abstract

Purpose: This study aimed to systematically map elements of care and respective outcomes described in the literature for different models of post-treatment care for survivors of childhood cancer. 

Methods: MEDLINE, CINAHL, and Embase were searched with combinations of free text terms, synonyms, and MeSH terms using Boolean operators and are current to January 2024. We included studies that described post-treatment cancer survivorship models of care and reported patient or service level elements of care or outcomes, which we mapped to the Quality of Cancer Survivorship Care Framework domains. 

Results: Thirty-eight studies with diverse designs were included representing 6101 childhood cancer survivors (or their parent/caregiver) and 14 healthcare professionals. A diverse range of models of care were reported, including paediatric oncologist-led long-term follow-up, multi-disciplinary survivorship clinics, shared-care, and primary care-led follow-up. Elements of care at the individual level most commonly included surveillance for cancer recurrence as well as assessment of physical and psychological effects. At the service level, satisfaction with care was frequently reported but few studies reported how treatment-related-late effects were managed. The evidence does not support one model of care over another. 

Conclusions: Gaps in evidence exist regarding distal outcomes such as costs, health care utilization, and mortality, as well as understanding outcomes of managing chronic disease and physical or psychological effects. The findings synthesized in this review provide a valuable reference point for future service planning and evaluation. 

Implications for Cancer Survivors: Decades of research highlight the importance of survivorship care for childhood cancer survivors who are at risk of serious treatment-related late effects. This review emphasizes there is no single, ‘one-size fits all’ approach for delivering such care to this vulnerable population.

Original languageEnglish
Number of pages17
JournalJournal of Cancer Survivorship
Early online date9 May 2024
DOIs
Publication statusE-pub ahead of print - 9 May 2024

Keywords

  • Cancer survivorship
  • Follow-up studies
  • Models of care
  • Paediatric
  • Patient-reported outcome measures
  • Survivorship

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