Evidence map›Paper›PMID 36130146›Full record

ReviewJCO oncology practice2023

Patient Understanding of Tumor Genomic Testing: A Quality Improvement Effort.

Leigha Senter, Deloris Veney, Taylor Surplus, Marcy Haynam, Elizabeth J Adams, Heather Hampel, Amanda E Toland, Carolyn J Presley, Tasleem J Padamsee, Clara N Lee and 2 more

Abstract readReview
In one paragraph

Review in JCO oncology practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Leigha SenterDivision of Human Genetics, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, OH.
Deloris VeneyDivision of Medical Oncology, Ohio State University Comprehensive Cancer Center, Columbus, OH.
Taylor SurplusSchool of Communication, Ohio State University, Columbus, OH.ORCID 0000-0002-8765-7616
Marcy HaynamDivision of Medical Oncology, Ohio State University Comprehensive Cancer Center, Columbus, OH.
Elizabeth J AdamsDivision of Medical Oncology, Ohio State University Comprehensive Cancer Center, Columbus, OH.
Heather HampelDivision of Human Genetics, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, OH.ORCID 0000-0001-7558-9794
Amanda E TolandDivision of Human Genetics, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, OH.ORCID 0000-0002-0271-1792
Carolyn J PresleyDivision of Medical Oncology, Ohio State University Comprehensive Cancer Center, Columbus, OH.ORCID 0000-0002-2607-5639
Tasleem J PadamseeDivision of Health Services Management and Policy, College of Public Health, The Ohio State University, Columbus, OH.ORCID 0000-0001-6644-8084
Clara N LeeRecruitment, Intervention and Survey Shared Resource, Ohio State University Comprehensive Cancer Center, Columbus, OH.
Shelly R HovickSchool of Communication, Ohio State University, Columbus, OH.
Daniel G StoverDivision of Medical Oncology, Ohio State University Comprehensive Cancer Center, Columbus, OH.ORCID 0000-0001-9003-8165

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
The OSU Center for Clinical and Translational Science: Advancing Today's Discoveries to Improve HealthUL1TR002733 · NCATS · OHIO STATE UNIVERSITY · PI RINGEL, MATTHEW D · 2018 to 2022
$28.9M
Impact of germline variants on racial and ethnic differences in somatic mutation frequencyR01CA215151 · NCI · OHIO STATE UNIVERSITY · PI TOLAND, AMANDA EWART · 2018 to 2022
$1.8M
Assay Validation of Cell-Free DNA Shallow Whole Genome Sequencing To Determine 'Tumor Fraction' in Advanced CancersUH3CA239105 · NCI · BROAD INSTITUTE, INC. · PI ADALSTEINSSON, VIKTOR, LENNON, NIALL JOHN · 2022 to 2024
$762k
Video Intervention to Address Pre-Test Patient Education for Tumor Genomic TestingR21CA259985 · NCI · OHIO STATE UNIVERSITY · PI SENTER-JAMIESON, LEIGHA, STOVER, DANIEL G. · 2021 to 2021
$396k
Assay Validation of Cell-Free DNA Shallow Whole Genome Sequencing To Determine 'Tumor Fraction' in Advanced CancersUH2CA239105 · NCI · BROAD INSTITUTE, INC. · PI ADALSTEINSSON, VIKTOR, LENNON, NIALL JOHN · 2020 to 2021
$321k
NCATS NIH HHS UL1 TR002733NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA215151NCI NIH HHS R21 CA259985NCI NIH HHS UH2 CA239105NCI NIH HHS UH3 CA239105
6 · The paper itself

Abstract

purposeTumor genomic testing (TGT) has become increasingly adopted as part of standard cancer care for many cancers. Despite national guidelines around patient education before TGT, available evidence suggests that most patients' understanding of genomics remains limited, particularly lower-income and minority patients, and most patients are not informed regarding potential incidental germline findings.

methodsTo investigate and address limitations in patient understanding of TGT results, a Plan-Do-Study-Act (PDSA) approach is being used to assess needs, identify opportunities for improvement, and implement approaches to optimize patient education. We reviewed published guidelines related to pre-TGT provider-patient education and to identify key points (Plan). A provider quality improvement survey was completed (Do), which highlighted inconsistency in pre-TGT discussion practice across providers and minimal discussion with patients regarding the possibility of incidental germline findings.

resultsPatient focus groups and interviews (N = 12 patients) were completed with coding of each transcript (Study), which revealed themes including trouble differentiating TGT from other forms of testing, yet understanding that results could tailor therapy. The integration of data across this initial PDSA cycle identified consistent themes and opportunities, which were incorporated into a patient-directed, concise animated video for pre-TGT education (Act), which will form the foundation of a subsequent PDSA cycle. The video addresses how TGT may/may not inform treatment, the process for TGT using existing tissue or liquid biopsy, insurance coverage, and the potential need for germline genetics follow-up because of incidental findings.

conclusionThis PDSA cycle reveals key gaps and opportunities for improvement in patient education before TGT.

Indexed as

NeoplasmsQuality ImprovementGenomicsHumans

Identifiers

PMID36130146
PMCPMC10166357

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.