The end of cancer treatment experience for children, adolescents, and their parents: A systematic review of the literature
Abstract
PROBLEM IDENTIFICATION: To date, there is limited study of the end of treatment (EOT) transition experiences and needs of children/adolescents with cancer and their parents. LITERATURE SEARCH: A systematic search identified primary research focusing on EOT, describing child, adolescent, and parental perceptions, experiences, and needs during this transition period. Of 170 articles identified, 22 met inclusion criteria. DATA EVALUATION/SYNTHESIS: Studies were appraised for level and quality of evidence. Narrative synthesis was performed to extract themes and integrate the literature. Family members' perceived needs, factors influencing the EOT experience, and consequences of this transition emerged as themes. CONCLUSIONS: Uncertainty and heightened anxiety at EOT highlight the need for increased education and support for family members. Family functioning and distress influence the EOT experience, with variable effects on each family member. There is a call for individualized interventions to promote coping and positive outcomes.
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Parents/caregivers of childhood cancer survivors can experience poor quality of life, anxiety, depression, loneliness, and fear of their child's cancer recurring.
“Despite the benefits of cancer treatment, this can be a vulnerable time for parents/caregivers, who can experience poor quality of life (QOL),_ENREF_9 anxiety, depression, loneliness _ENREF_8 [3,4,5,6,7], and fear of their child’s cancer recurring [4,5].”
From Providing psychological support to parents of childhood cancer survivors: ‘cascade’ intervention trial results and lessons for the future (2021) · cites this paper as [6]
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- Authors
- Conway Keller, M., King, C., Hart, L., Engelke, K., Needham, A., Holden, E., Foy, K., & Lucas, R.
- Affiliations
- Division of Hematology-Oncology, Connecticut Children’s Medical Center, Hartford, Connecticut, USA
- Connecticut Children's Medical Center (US)
- University of Connecticut (US)
- Venue
- Journal of Psychosocial Oncology
- Publisher
- Informa UK Limited
- Published
- 2020-06-30
- Volume
- 38
- Issue
- 5
- Pages
- 573-591
- ISSN
- 0734-7332 (ISSN-L)
- 1540-7586
- OpenAlex
- W3040064588
- Cited by
- 31
- References
- 40
- Citations by year
- 2026: 1 · 2025: 11 · 2024: 6 · 2023: 4 · 2022: 6 · 2021: 1 · 2020: 1
- FWCI
- 0.66
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Psychosocial Oncology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Childhood Cancer Survivors' Quality of Life
- Social Sciences › Sociology and Political Science › Family Support in Illness
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative and Oncologic Care
- Keywords
- childhood cancer, adolescent cancer, parents of children with cancer, patient and family experiences, anxiety, uncertainty, family functioning, family distress, coping, psychosocial support, personalized interventions
- MeSH terms
- Adolescent, Psychology, Adolescent, Child, Psychology, Child, Humans, Neoplasms, Parents
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