Evidence map›Paper›PMID 37897815›Full record

ArticleJCO precision oncology2023

Exploring Stakeholders' Perspectives on Implementing Universal Germline Testing for Colorectal Cancer: Findings From a Clinical Practice Survey.

Linda Rodgers-Fouche, Sanjeevani Arora, Charité Ricker, Dan Li, Maheen Farooqi, Francesc Balaguer, Mev Dominguez-Valentin, Jose G Guillem, Priyanka Kanth, David Liska and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in JCO precision oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 19% of its field
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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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

16 authors at 11 institutions in 5 countries.

Linda Rodgers-FoucheCenter for Cancer Risk Assessment, Massachusetts General Hospital, Boston, MA.ORCID 0000-0002-3956-5821
Sanjeevani AroraCancer Prevention and Control Program, Fox Chase Cancer Center, Philadelphia, PA.
Charité RickerDivision of Medical Oncology, Department of Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA.
Dan LiDepartment of Gastroenterology, Kaiser Permanente Medical Center, Santa Clara, CA.ORCID 0000-0002-2691-5175
Maheen FarooqiDivision of Medical Oncology, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, CA.
Francesc BalaguerDepartment of Gastroenterology, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), University of Barcelona, Barcelona, Spain.ORCID 0000-0002-0206-0539
Mev Dominguez-ValentinDepartment of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, Oslo, Norway.ORCID 0000-0001-7856-0057
Jose G GuillemDepartment of Surgery, University of North Carolina, Chapel Hill, NC.ORCID 0009-0002-3510-8276
Priyanka KanthDepartment of Gastroenterology, MedStar Georgetown University Hospital, Washington, DC.ORCID 0000-0001-9303-1516
David LiskaDepartment of Colorectal Surgery, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.ORCID 0000-0002-8632-6065
Joshua MelsonDivision of Gastroenterology, University of Arizona Cancer Center, Tucson, AZ.
Kathryn A MrazGrey Genetics, Brooklyn, NY.ORCID 0000-0001-9824-8159
Brian H ShirtsDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA.ORCID 0000-0002-7188-6764
Eduardo VilarDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-6404-3761
Bryson W KatonaDivision of Gastroenterology and Hepatology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.ORCID 0000-0001-8186-9119
Rachel HodanCancer Genetics, Stanford Health Care, Palo Alto, CA.ORCID 0000-0003-2887-4079
Fox Chase Cancer Center · USUniversity of Southern California · USCleveland Clinic · USGeorgetown University · USHospital Clínic de Barcelona · ESKaiser Permanente Santa Clara Medical Center · USMassachusetts General Hospital · USNorwegian Cancer Society · NOUniversity of Arizona · USUniversity of North Carolina at Chapel Hill · USUniversity of Washington · US

Funding

Validation of blood-based predictive biomarkers of therapeutic response to neoadjuvant chemoradiation therapy in patients with locally advanced rectal cancerUH2CA271230 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI ARORA, SANJEEVANI, MEYER, JOSHUA E. · 2022 to 2023
$512k
NCI NIH HHS UH2 CA271230
6 · The paper itself

Abstract

purposeNew guidelines recommend considering germline genetic testing for all patients with colorectal cancer (CRC). However, there is a lack of data on stakeholders' perspectives on the advantages and barriers of implementing universal germline testing (UGT). This study assessed the perspectives of members of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer (CGA-IGC) regarding the implementation of UGT for patients with CRC, including readiness, logistics, and barriers.

methodsA cross-sectional survey was sent to 317 active members of CGA-IGC. The survey included sections on demographics, clinical practice specialty, established institutional practices for testing, and questions pertaining to support of and barriers to implementing UGT for patients with CRC.

resultsEighty CGA-IGC members (25%) participated, including 42 genetic counselors (53%) and 14 gastroenterologists (18%). Forty-seven (59%) reported an academic medical center as their primary work setting, and most participants (56%) had more than 10 years of clinical practice. Although most participants (73%) supported UGT, 54% indicated that changes in practice would be required before adopting UGT, and 39% indicated that these changes would be challenging to implement. There was support for both genetics and nongenetics providers to order genetic testing, and a majority (57%) supported a standardized multigene panel rather than a customized gene panel. Key barriers to UGT implementation included limited genetics knowledge among nongenetics providers, time-consuming processes for obtaining consent, ordering tests, disclosing results, and lack of insurance coverage.

conclusionThis study demonstrates wide support among hereditary GI cancer experts for implementation of UGT for patients with CRC. However, alternative service delivery models using nongenetics providers should be considered to address the logistical barriers to UGT implementation, particularly the growing demand for genetic testing.

Indexed as

Colorectal NeoplasmsGenetic TestingCross-Sectional StudiesHumansSurveys and Questionnaires

Identifiers

PMID37897815
PMCPMC10860957
OpenAlexW4388034546

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.