Evidence map›Paper›PMID 37258251›Full record

ArticleJournal of clinical pathology2024

Landscape of cancer biomarker testing in England following genomic services reconfiguration: insights from a nationwide pathologist survey.

Phillipe Taniere, Andrew G Nicholson, John R Gosney, Maria Angeles Montero Fernandez, Danielle Bury, David Allan Moore, Eldo Verghese, Irshad Soomro, Leena Joseph, Nidhi Bhatt and 4 more

Abstract read
In one paragraph

Article in Journal of clinical pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  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

14 authors.

Phillipe TaniereHistopathology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK phillipe.taniere@uhb.nhs.uk.ORCID http://orcid.org/0000-0002-4638-4551
Andrew G NicholsonRespiratory Pathology, National Heart and Lung Institute, Imperial College London, London, UK.
John R GosneyCellular Pathology, Royal Liverpool University Hospital, Liverpool, UK.
Maria Angeles Montero FernandezHistopathology, Manchester University NHS Foundation Trust, Manchester, UK.
Danielle BuryHistopathology, Blackpool Teaching Hospitals NHS Foundation Trust, Blackpool, UK.
David Allan MooreCellular Pathology, University College London Cancer Institute, London, UK.ORCID http://orcid.org/0000-0001-9116-346X
Eldo VergheseHistopathology, St James's University Hospital, Leeds, UK.
Irshad SoomroHistopathology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Leena JosephHistopathology, Manchester University NHS Foundation Trust, Manchester, UK.
Nidhi BhattCellular Pathology, North Bristol NHS Trust, Westbury on Trym, UK.
Patrizia ViolaCellular Pathology, Imperial College Healthcare NHS Trust, London, UK.
Rozinder BainsNovartis Pharmaceuticals UK Ltd, London, UK.
Adrienne G LanctotNovartis Pharmaceuticals UK Ltd, London, UK.
Jacqueline RyanNovartis Pharmaceuticals UK Ltd, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsCancer diagnostics have been evolving rapidly. In England, the new National Health Service Genomic Medicine Service (GMS) provides centralised access to genomic testing via seven regional Genomic Laboratory Hubs. The PATHways survey aimed to capture pathologists' experience with current diagnostic pathways and opportunities for optimisation to ensure equitable and timely access to biomarker testing.

methodsA nationwide survey was conducted with consultant pathologists from regional laboratories, via direct interviews based on a structured questionnaire. Descriptive analysis of responses was undertaken using quantitative and qualitative methods.

resultsFifteen regional centres completed the survey covering a median population size of 2.5 (1.9-3.6) million (each for n=12). The median estimated turnaround time (calendar days) for standard molecular markers in melanoma, breast and lung cancers ranged from 2 to 3 days by immunohistochemistry (excluding NTRKfus in breast and lung cancers, and PD-L1 in melanoma) and 6-15 days by real-time-PCR (excluding KIT for melanoma), to 17.5-24.5 days by next-generation sequencing (excluding

conclusionOur survey highlighted the role of regional pathology within the evolving diagnostic landscape in England. Notable recommendations included improved communication and education, active stakeholder engagement, and tackling informatics barriers.

Indexed as

Biomarkers, TumorPathologistsEnglandGenomicsHealth Care SurveysHumansNeoplasmsPathology, MolecularState MedicineSurveys and QuestionnairesBiomarkers, TumorCANCERDIAGNOSTICSHealth Services

Identifiers

PMID37258251
PMCPMC11228219

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.