Treatment Setting, Clinical Trial Enrollment, and Subsequent Outcomes Among Adolescents With Cancer: A Literature Review
Open accessAbstract
BACKGROUND: There has been an overall improvement in survival rates for persons with cancer over the past 35 years. However, these gains are less prevalent among adolescents with cancer aged 15 to 19 years, which may be due to lower clinical trial enrollment among adolescents with cancer. METHODS: We conducted a literature review to assess current research regarding clinical trial enrollment and subsequent outcomes among adolescents with cancer. The search included English-language publications that reported original data from January 1985 to October 2011. RESULTS: The search identified 539 records. Of these 539 records, there were 30 relevant original research articles. Multiple studies reported that adolescents with cancer are enrolled in clinical trials at lower rates compared with younger children and older adults. Treatment setting, physician type, and institution type may all be factors in the low enrollment rate among adolescents. Few data focused solely on adolescents, with many studies combining adolescents with young adults. The number of available studies related to this topic was limited, with significant variability in study design, methods, and outcomes. CONCLUSIONS: This literature review suggests that adolescents with cancer are not treated at optimal settings and are enrolled in clinical trials at low rates. This may lead to inferior treatment and poor subsequent medical and psychosocial outcomes. The scarcity in data further validates the need for additional research focusing on this population.
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More than 60% of adolescents and young adults experience adverse physical, psychosocial, or behavioral outcomes months or years after cancer treatment.
“Over 60% of adolescents and young adults will suffer adverse physical, psychosocial, and/or behavioral outcomes months or years after completion of cancer treatment [3–6].”
From A Hope-based intervention to address disrupted goal pursuits and quality of life among young adult cancer survivors (2020) · cites this paper as [6]
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- Authors
- Tai, E., Buchanan, N., Westervelt, L., Elimam, D., & Lawvere, S.
- Affiliations
- Centers for Disease Control and Prevention (US)
- SciMetrika LLC, Research Triangle Park, North Carolina; and
- University of North Carolina at Chapel Hill (US)
- Corresponding author
- Tai, Eric
- ORCID
- Tai, Eric
- Venue
- Pediatrics
- Publisher
- American Academy of Pediatrics (AAP)
- Published
- 2014-06-01
- Volume
- 133
- Issue
- Supplement_3
- Pages
- S91-S97
- ISSN
- 0031-4005 (ISSN-L)
- 1098-4275
- PMC
- PMC6075704
- OpenAlex
- W2121542492
- Cited by
- 39
- References
- 47
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 2 · 2023: 3 · 2022: 1 · 2021: 4 · 2020: 3 · 2019: 8 · 2018: 7 · 2017: 3 · 2016: 5 · 2015: 1
- FWCI
- 0.47
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- PEDIATRICS (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (CC999999)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Acute Lymphoblastic Leukemia research
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Childhood Cancer Survivors' Quality of Life
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Ethics in Clinical Research
- Keywords
- adolescent cancer, clinical trial recruitment, treatment setting, institutional type, psychosocial outcomes, medical outcomes, young adult cancer, clinical trial access
- MeSH terms
- Adolescent, Clinical Trials as Topic, Humans, Neoplasms, Survival Rate, Treatment Outcome, Patient Selection, Young Adult
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