Evidence map›Paper›PMID 39546086›Full record

ArticleFamilial cancer2024

Mainstreaming cancer genetics: feasibility of an advanced nurse practitioner-led service diagnosing Lynch syndrome from colorectal cancer in Ireland.

Mechelle Loughrey, Lauren V O'Connell, Lynda McSorley, Sean Martin, Ann Hanly, Des C Winter, Ian M Frayling, Kieran Sheahan, Rory Kennelly

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Article in Familial cancer, 2024. 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
–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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. CANO Position Statement: Genomics-informed oncology nursing.Canadian oncology nursing journal = Revue canadienne de nursing oncologique · 2026
    Article
4 · The record

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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

9 authors.

Mechelle LoughreyCentre for Colorectal Disease, St Vincent's University Hospital, Elm Park, Merrion Rd, Dublin 4, Ireland. mechelleloughrey@svhg.ie.ORCID 0000-0002-7311-7360
Lauren V O'ConnellCentre for Colorectal Disease, St Vincent's University Hospital, Elm Park, Merrion Rd, Dublin 4, Ireland.
Lynda McSorleyDepartment of Medical Oncology, St Vincent's University Hospital, Elm Park, Merrion Rd, Dublin 4, Ireland.
Sean MartinCentre for Colorectal Disease, St Vincent's University Hospital, Elm Park, Merrion Rd, Dublin 4, Ireland.
Ann HanlyCentre for Colorectal Disease, St Vincent's University Hospital, Elm Park, Merrion Rd, Dublin 4, Ireland.
Des C WinterCentre for Colorectal Disease, St Vincent's University Hospital, Elm Park, Merrion Rd, Dublin 4, Ireland.
Ian M FraylingDepartment of Pathology, St Vincent's University Hospital, Elm Park, Merrion Rd, Dublin 4, Ireland.
Kieran SheahanDepartment of Pathology, St Vincent's University Hospital, Elm Park, Merrion Rd, Dublin 4, Ireland.
Rory KennellyCentre for Colorectal Disease, St Vincent's University Hospital, Elm Park, Merrion Rd, Dublin 4, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is a common cancer in Ireland. Of all CRCs, 2-4% are attributable to Lynch Syndrome (LS), the most common CRC predisposition syndrome. LS is caused by constitutional pathogenic variants (PVs) affecting mismatch repair (MMR) genes with resultant MMR protein deficiency (dMMR). Screening of all CRCs with MMR immunohistochemistry (IHC) testing is advocated to increase the detection of LS. However, successful implementation requires appropriate downstream management. In Ireland the traditional pathway involves referral to cancer genetics services to assess eligibility for genetic testing. Cancer genetics services in Ireland face many challenges in providing uniform access to timely healthcare with current wait times for assessment in excess of 1 year. An increasingly adopted pathway is that of mainstreaming, whereby genetic testing is managed locally by a multidisciplinary team member. Our institution therefore implemented an Advanced Nurse Practitioner (ANP)-led service with responsibility for the LS Diagnostic Pathway and mainstream genetic testing. Data was extracted from a prospectively maintained database of all newly diagnosed CRC patients discussed at our institutions CRC multidisciplinary meeting (MDM) between January 1st, 2023, and May 31st, 2024. MMR IHC testing was performed in 97.9% of the 385 patients diagnosed with CRC. The median time from histological confirmation of CRC to the availability of the MMR IHC report was 6 days. All 51 patients (100%) who required sequential tumor testing underwent BRAF V600 ± MLH1 promoter methylation testing. Additionally, 100% of the 14 patients eligible for mainstream genetic testing were referred to the ANP-led genetics service. The median time from the initial MDM discussion to the initiation of genetic testing was 69 days, while the median time from testing to the availability of results was 19 days. Patients received their results within a median of 21 days. MMR IHC testing increases the detection of LS through identification of dMMR tumours. Successful downstream delivery of clinical services, however, requires appropriate subsequent management, in a resource-limited environment. Our institutional experience demonstrates the feasibility, efficiency, and effectiveness of an ANP-led mainstreaming model of care for hereditary colorectal cancer.

Indexed as

Colorectal Neoplasms, Hereditary NonpolyposisFeasibility StudiesGenetic TestingNurse PractitionersAdultAgedColorectal NeoplasmsDNA Mismatch RepairFemaleHumansIrelandMaleMiddle AgedMutL Protein Homolog 1Proto-Oncogene Proteins B-rafReferral and ConsultationBRAF protein, humanMLH1 protein, humanMutL Protein Homolog 1Proto-Oncogene Proteins B-rafAdvanced nurse practitionerCancer geneticsColorectal cancerLynch syndromeMainstreaming

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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.