Evidence map›Paper›PMID 36178922›Full record

ArticleJCO oncology practice2022

Ineligible, Unaware, or Uninterested? Associations Between Underrepresented Patient Populations and Retention in the Pathway to Cancer Clinical Trial Enrollment.

Nicole E Caston, Fallon Lalor, Jaclyn Wall, Jesse Sussell, Shilpen Patel, Courtney P Williams, Andres Azuero, Rebecca Arend, Margaret I Liang, Gabrielle B Rocque

Abstract read
In one paragraph

Article in JCO oncology practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Nicole E CastonDivision of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0001-7474-6110
Fallon LalorDivision of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL.
Jaclyn WallDivision of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0002-9054-1905
Jesse SussellGenentech, San Francisco, CA.
Shilpen PatelGenentech, San Francisco, CA.
Courtney P WilliamsDivision of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0001-5328-7517
Andres AzueroUAB School of Nursing, Birmingham, AL.ORCID 0000-0001-9883-1424
Rebecca ArendDivision of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL.
Margaret I LiangDivision of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0001-9229-5181
Gabrielle B RocqueDivision of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0003-4188-9785

Funding

Treatment of HIV- and HIV+ Patients with HPV16+ CIN2/3 Using pNGLV4a-hCRTE6E7L2 DNA vaccine administered intramuscularly via electroporationP50CA098252 · NCI · JOHNS HOPKINS UNIVERSITY · PI TZYY-CHOOU WU · 2003 to 2026
$53.5M
Evaluating the implementation and impact of navigator-delivered ePRO home symptom monitoring and managementR01NR019058 · NINR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ROCQUE, GABRIELLE · 2021 to 2025
$3.1M
AHRQ HHS T32 HS013852NCI NIH HHS P50 CA098252NINR NIH HHS R01 NR019058
6 · The paper itself

Abstract

purposeCancer clinical trials can benefit current and future patients; however, Black patients, rural residents, and patients living in disadvantaged areas are often underrepresented. Using an adapted version of Unger and colleagues' model of the process of clinical trial enrollment, we evaluated the relationship between underrepresented patient populations and trial end points.

methodsThis retrospective study included 512 patients with breast or ovarian cancer who were prescribed a therapeutic drug at the University of Alabama at Birmingham from January 2017 to February 2020. Patient eligibility was assessed using open clinical trials. We estimated odds ratios and 95% CIs using logistic regression models to examine the relationship between underrepresented patient populations and trial enrollment end points: eligibility, interest, offer, enrollment, and declining enrollment.

resultsOf the patients in our sample, 27% were Black, 18% were rural residents, and 19% lived in higher disadvantaged neighborhoods. In adjusted models, each comparison group had similar odds of being eligible for a clinical trial. Black versus White patients had 0.40 times the odds of interest in clinical trials and 0.56 times the odds of enrollment. Patients living in areas of higher versus lower disadvantage had 0.46 times the odds of enrolling and 3.40 times the odds of declining enrollment when offered.

conclusionEligibility did not drive clinical trial enrollment disparities in our sample; however, retention in the clinical trial enrollment process appears to vary by group. Additional work is needed to understand how interventions can be tailored to each population's specific needs.

Indexed as

NeoplasmsEligibility DeterminationHumansLogistic ModelsRetrospective StudiesRural Population

Identifiers

PMID36178922
PMCPMC9653198

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.