Cited by 41Ethics in Clinical ResearchChildhood Cancer Survivors' Quality of LifeHealth and Medical Research Impacts

Clinical research participation among adolescent and young adults at an NCI-designated Comprehensive Cancer Center and affiliated pediatric hospital

Open access
Sanford, Stacy D., Beaumont, Jennifer L., Snyder, Mallory A., Reichek, Jennifer, Salsman, John M.·2017·Supportive Care in Cancer

Abstract

Purpose Minimal clinical trial participation among adolescents and young adults (AYAs) with cancer limits scientific progress and ultimately their clinical care and outcomes. These analyses examine the current state of AYA clinical research participation at a Midwestern comprehensive cancer center and affiliated pediatric hospital to advise program development and increase availability of trials and AYA participation. Enrollment is examined across all diagnoses, the entire AYA age spectrum (15-39), and both cancer therapeutic and supportive care protocols.Methods his study was a retrospective review of electronic medical records via existing databases and registries for all AYAs. Data were collected for AYAs seen by an oncologist at the adult outpatient cancer center or at the pediatric hospital between the years 2010 and 2014. Descriptive statistics and logistic regression analyses were conducted to characterize this sample.Results In the pediatric setting, 42.3% of AYAs were enrolled in a study compared to 11.2% in the adult setting. Regression analyses in the pediatric setting revealed that AYAs with private insurance or Caucasian race were more likely to participate. Within the adult setting, ethnicity, race, insurance, and diagnosis were associated with study participation; 54.8% of study enrollments were for cancer therapeutic and 43.4% for supportive care studies.Conclusions These results are comparable to previously published data and support the need for new local and national AYA initiatives to increase the availability of and enrollment in therapeutic clinical trials. The same is true for supportive care studies which play a crucial role in improving quality of life.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1007/s00520-016-3558-7

Cites

18 of 18 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 1

  1. [1]Adolescent and Young Adult Oncology Progress Review Group 2006 Closing the gap: research and care imperatives for adolescents and young adults with cancer USA National Cancer Institute Bethesda

Cited by

Sorted by citations

Authors
Sanford, S. D., Beaumont, J. L., Snyder, M. A., Reichek, J., & Salsman, J. M.
Affiliations
  • Northwestern University (US)
  • Wake Forest University Health Sciences (US)
Corresponding author
Sanford, Stacy D.
Venue
Supportive Care in Cancer
Published
2017-01-10
Volume
25
Issue
5
Pages
1579-1586
ISSN
  • 0941-4355 (ISSN-L)
  • 1433-7339
OpenAlex
W2568897144
Cited by
41
References
18
Citations by year
2026: 1 · 2025: 4 · 2023: 2 · 2022: 4 · 2021: 11 · 2020: 3 · 2019: 8 · 2018: 8
FWCI
4.87
Type
journal article
Language
en
Open access
Locations
  • Supportive Care in Cancer (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Cancer Institute (K07CA158008)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Ethics in Clinical Research
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Childhood Cancer Survivors' Quality of Life
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Health and Medical Research Impacts
Keywords
adolescents and young adults, cancer clinical trials, clinical trial recruitment, barriers to research participation, insurance status, racial and ethnic disparities, pediatric oncology, comprehensive cancer center, quality of life
MeSH terms
Adolescent, Adult, Cancer Care Facilities, Female, Hospitals, Pediatric, Humans, Male, Neoplasms, Quality of Life, Registries, Retrospective Studies, United States, Databases, Factual, Biomedical Research, National Cancer Institute (U.S.), Young Adult

About these checks

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.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review