Evidence map›Paper›PMID 38343462›Full record

ArticleProceedings (Baylor University. Medical Center)2024

Colorectal cancer genetic referral: Are we doing enough?

Whitnee C Broyles, Priyanka Narvekar, Hanjoo Lee, James W Fleshman, Alessandro Fichera, Katerina K O Wells

Open access · greenAbstract read
In one paragraph

Article in Proceedings (Baylor University. Medical Center), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 2 institutions in 1 country.

Whitnee C BroylesDepartment of Surgery, Baylor University Medical Center, Dallas, Texas, USA.ORCID https://orcid.org/0000-0002-4350-0991
Priyanka NarvekarTexas A&M School of Medicine, Baylor University Medical Center, Dallas, Texas, USA.
Hanjoo LeeDivision of Colon & Rectal Surgery, David Geffen School of Medicine at UCLA, Harbor-UCLA Medical Center, Los Angeles, California, USA.
James W FleshmanDivision of Colon and Rectal Surgery, Department of Surgery, Baylor University Medical Center, Dallas, Texas, USA.
Alessandro FicheraDivision of Colon and Rectal Surgery, Department of Surgery, Baylor University Medical Center, Dallas, Texas, USA.
Katerina K O WellsDivision of Colon and Rectal Surgery, Department of Surgery, Baylor University Medical Center, Dallas, Texas, USA.
Baylor University Medical Center · USUCLA Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Guidelines are published for referral to genetic counseling and multigene panel genetic testing for colorectal cancer. We hypothesize that these guidelines are not recognized in practice, resulting in the underreferral of patients to genetic counseling. We aimed to investigate the clinical impact of these guidelines. Methods: This was a retrospective cohort study conducted using a single academic-institution colorectal cancer patient registry. The registry included all patients ≥18 years old with a pathologic diagnosis of colon cancer, rectal cancer, or polyposis from January 2018 to January 2020 with complete chart data to determine inclusion into the genetic referral cohort. Results: Out of 225 colon cancer patients, 92 met criteria for referral to genetic testing, but only 56 patients obtained referral and 39 completed testing. For rectal cancer, 29 out of 127 patients met criteria for referral, but only 11 obtained referral and 8 completed testing. Actionable variants, defined as pathogenic or likely pathogenic, were identified in 18 colon cancer and 5 rectal cancer patients. Age made a significant difference in the referral rate for colon cancer ( Conclusion: Our study demonstrates poor adherence to guideline-based genetic testing. These data emphasize the need for more consistent referral to genetic testing for diagnosis of underlying inherited cancer syndromes.

Indexed as

Colorectal neoplasmsevidence-based medicinegenetic testinghereditary nonpolyposis

Identifiers

PMID38343462
PMCPMC10857445
OpenAlexW4391218491

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.