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Psychological Outcomes, Health-Related Quality of Life, and Neurocognitive Functioning in Survivors of Childhood Cancer and Their Parents
Open accessAbstract
Childhood cancer disrupts the lives of patients and their families and affects acute and long-term psychological health. This article summarizes (1) psychological challenges, including depression, anxiety, worries, and posttraumatic stress, as well as positive outcomes such as benefit finding and posttraumatic growth in young survivors and parents; (2) health-related quality of life; (3) interventions to support survivors and parents with psychological difficulties; and (4) neurocognitive problems and interventions to help alleviate them. Although many survivors and parents fare well in the long term, many survivors may benefit from interventions. Interventions should be further evaluated and integrated into routine clinical care.
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“With the exception of the eSCCIP [23], most interventions are also implemented face-to-face, limiting benefits to rural-remote families [7,25,27,33].”
From Providing psychological support to parents of childhood cancer survivors: ‘cascade’ intervention trial results and lessons for the future (2021) · cites this paper as [7]
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“In line with other studies, we found that CCS with certain socio-demographic characteristics, including female sex, lower educational attainment, and unemployment, along with cancer-related medical characteristics, such as a CNS tumor diagnosis, reported poorer psychosocial outcomes [4, 8].”
From Risk and Protective Factors of Psychosocial Functioning in Survivors of Childhood Cancer: Results of the DCCSS-LATER Study (2024) · cites this paper as [4]
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“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 [7]
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“However, certain subgroups report worse HRQOL compared to general population norms, and experience symptoms like anxiety, depression, and posttraumatic stress [4, 5].”
From Risk and Protective Factors of Psychosocial Functioning in Survivors of Childhood Cancer: Results of the DCCSS-LATER Study (2024) · cites this paper as [4]
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“However, few interventions have implemented evidence-based treatments [31,32] and many have not been evaluated with rigorous research designs in pediatric oncology [7,24,25,27].”
From Providing psychological support to parents of childhood cancer survivors: ‘cascade’ intervention trial results and lessons for the future (2021) · cites this paper as [7]
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Long-term care for people treated for cancer during childhood and adolescence
Tonorezos, E. S., Cohn, R. J., Glaser, A., Lewin, J. H., Poon, E. Y. L., Wakefield, C. E., & Oeffinger, K. C. (2022) · The Lancet · doi:10.1016/s0140-6736(22)00460-3 · Cited by 122
Self-citationvan Kalsbeek, R. J., Hudson, M. M., Mulder, R. L., Ehrhardt, M. J., Green, D. M., Mulrooney, D. A., Hakkert, J., den Hartogh, J. G., Nijenhuis, A., van Santen, H. M., et al. (2023) · Nature Medicine · doi:10.1038/s41591-023-02339-y · Cited by 54
Self-citationFeijen, E. A. M., Teepen, J. C., van Dulmen‐den Broeder, E., van den Heuvel‐Eibrink, M. M., van der Heiden‐van der Loo, M., van der Pal, H. J. H., de Vries, A. C. H., Louwerens, M., Bresters, D., Versluys, B., et al. (2023) · Pediatric Blood & Cancer · doi:10.1002/pbc.30212 · Cited by 41
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Metadata
- Authors
- Michel, G., Brinkman, T. M., Wakefield, C. E., & Grootenhuis, M.
- Affiliations
- University of Lucerne (CH)
- St. Jude Children's Research Hospital (US)
- UNSW Sydney (AU)
- Princess Máxima Center (NL)
- Corresponding author
- Michel, Gisela
- Venue
- Pediatric Clinics of North America
- Publisher
- Elsevier BV
- Published
- 2020-12
- Volume
- 67
- Issue
- 6
- Pages
- 1103-1134
- ISSN
- 0031-3955 (ISSN-L)
- OpenAlex
- W3089288901
- Cited by
- 133
- References
- 89
- Citations by year
- 2026: 28 · 2025: 25 · 2024: 36 · 2023: 22 · 2022: 13 · 2021: 8 · 2020: 1
- FWCI
- 2.45
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Pediatric Clinics of North America (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Pure Amsterdam UMC (publishedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- Topics
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Childhood Cancer Survivors' Quality of Life
- Health Sciences › Medicine › Oncology › Cancer survivorship and care
- Social Sciences › Psychology › Clinical Psychology › Family Support in Illness
- Keywords
- childhood cancer survivors, parental caregivers, psychological outcomes, health-related quality of life, neurocognitive function, depression, anxiety, post-traumatic stress, benefit finding, posttraumatic growth, psychological intervention, neurocognitive interventions
- MeSH terms
- Cancer Survivors, Adaptation, Psychological, Humans, Mental Health, Parents, Quality of Life, Stress, Psychological
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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