Evidence map›Paper›PMID 42131761›Full record

ArticleNeuro-oncology practice2026

Transforming molecular neuropathology for adult brain tumor patients in the UK: Insights on implementation, adoption, and patient access (2021-2024).

Kathreena M Kurian, Andrew P Wright, Fereshteh Sari, Mayen Briggs, Camille Goetz, Ros Quinlivan, Katie Bushby, Richard Gilbertson, Nicky Huskens, Tessa Jowell Centre of Excellence for Adults Committee

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Article in Neuro-oncology practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Kathreena M KurianBrain Tumour Research Centre, Bristol Medical School, University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0003-0303-3716
Andrew P WrightTessa Jowell Brain Cancer Mission, London, UK.ORCID https://orcid.org/0009-0002-2143-9218
Fereshteh SariTessa Jowell Brain Cancer Mission, London, UK.
Mayen BriggsCambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Camille GoetzTessa Jowell Brain Cancer Mission, London, UK.
Ros QuinlivanUniversity College London Hospitals NHS Foundation Trust, London, UK.
Katie BushbyTessa Jowell Brain Cancer Mission, London, UK.
Richard GilbertsonCancer Research UK Cambridge Centre, Cambridge, UK.
Nicky HuskensTessa Jowell Brain Cancer Mission, London, UK.
Tessa Jowell Centre of Excellence for Adults Committee

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundMolecular neuropathology is evolving rapidly, driven by novel genomic technologies, national policies, and the urgent need for precision brain tumor care. Inequity in access to genomic testing highlighted in previous reports warrants further investigation. Methods: We analyzed anonymized data from 21 United Kingdom (UK) neuro-oncology centers (covering an estimated 84% of the population) collected in 2021 and 2024 via the Tessa Jowell Centre of Excellence for Adults program. We assessed trends in genomic testing (including methylation arrays, gene panels, whole genome sequencing [WGS]), tumor snap freezing, turnaround times (TATs), and auditing. Results: From 2021 to 2024, total genomic tests submitted across the 21 centers increased 128% from 2946 to 6730, while glioma cases increased 18% (from 3159 to 3722). Methylation arrays, gene panels, and WGS samples submitted rose by 342%, 174%, and 291%, respectively. Centers requesting WGS increased from 4/21 (19%) to 15/21 (71%), with 90% centers (19/21) reporting snap freezing of brain tumor samples in 2024 (mean 173, range 0-650 samples frozen per center). Mean molecular diagnosis TATs rose from 16 to 21 days; centers meeting a 14-day TAT dropped from 48% (10/21) to 30% (6/20). Auditing of TATs increased from 6/21 (29%) to 18/21 (86%). Conclusions: UK molecular neuropathology testing grew substantially 2021-2024. However, variations in testing and snap freezing, and bottlenecks in diagnostic TATs, emphasize the need for: (1) targeted training and investment in rapid technologies to ensure sustainable service delivery; (2) focus on remaining inequities and (3) continued engagement with national benchmarking initiatives.

Indexed as

brain tumorsgenomicsmolecular neuropathologyUK

Identifiers

PMID42131761
PMCPMC13161907

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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.