Evidence map›Paper›PMID 41744174›Full record

ArticleBJU international2026

The PRAGMATIC pathway - PRostate cancer diAGnosis and MAnagement Triage In Clinical care.

Abhishek Sharma, Teresa Campbell, Sagar Kanabar, Hannah Soanes, Ganesh Sathanapally, Anthony Bates, Rincy John, Charlotte Adams, Aisling Brassill, Bryony Lennon and 19 more

Abstract read
In one paragraph

Article in BJU international, 2026. 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
–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

0 citing papers in PubMed.

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

29 authors.

Abhishek SharmaDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.ORCID 0009-0009-3396-5937
Teresa CampbellDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Sagar KanabarDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Hannah SoanesDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Ganesh SathanapallyDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Anthony BatesDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Rincy JohnDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Charlotte AdamsDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Aisling BrassillQuality Improvement Team, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
Bryony LennonDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Sanjay SinhaOxford Transplant Centre, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Louise FlaxmanDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Vanessa von HasselnDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Philip CamilleriDepartment of Oncology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Ami SabharwalDepartment of Oncology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Philip CharltonDepartment of Oncology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Gerard AndradeDepartment of Oncology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Mark TuthillOxford Transplant Centre, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Andrew ProtheroeDepartment of Oncology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Alastair D LambDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Tom LeslieDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Aaron LeiblichDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Francisco LopezDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.ORCID 0000-0002-6498-2635
Clare VerrillDepartment of Cellular Pathology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
Fergus GleesonDepartment of Radiology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Ruth MacPhersonDepartment of Radiology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Freddie C HamdyDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Richard BellDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
Richard J BryantDepartment of Urology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.ORCID 0000-0002-8330-9251

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate whether nurse navigator-led triaging of high-risk patients may reduce prostate cancer (PCa) diagnosis and treatment times using an in-house bespoke PRostate cancer diAGnosis and MAnagement Triage In the Clinial care pathway (PRAGMATIC) triaging system, as locally advanced/metastatic disease should be diagnosed and treated rapidly, and UK targets allow 28 days for diagnosis, and 62 days to commence treatment. PATIENTS AND

methodsWe reviewed diagnosis and treatment timelines for patients undergoing 28/62-day investigation for suspected PCa at a tertiary unit in a 3-month period (2022). We then introduced nurse navigator-led triaging of urgent referrals and evaluated a subsequent 3-month period (2024), with streamlining for rapid investigation and treatment based on prostate-specific antigen, magnetic resonance imaging (MRI) staging, and histology. We hypothesised nurse navigator-led triaging would improve investigation and treatment times for high-risk localised, or locally advanced, or metastatic PCa.

resultsA total of 165 and 327 consecutive patients were on the 28/62-day PCa pathway in the pre- (2022) and post-nurse navigator-led (2024) triaging periods, respectively. The median time from referral to first appointment (8 vs 4 days), MRI (12 vs 6 days), MRI result (26 vs 17 days), biopsy decision (25 vs 16 days), biopsy procedure (48 vs 22 days), biopsy result communication (64 vs 44 fays), and prostate-specific membrane antigen positron emission tomography computed tomography staging scan (87 vs 56 days) was reduced following nurse navigator triaging of high-risk cases (all P < 0.001). The median time from referral to treatment for Gleason Grade Group ≥3, or T3, or ≥N1, or ≥M1 disease (104 vs 70 days; 49/75 [65.3%] vs 72/128 [56.3%] patients), and for M1b disease (47 vs 27 days; 15/75 [20%] vs 32/128 [25%] patients), was reduced (P < 0.05).

conclusionsNurse navigator-led triaging and stratification of the most clinically urgent suspected PCa cases was associated with improved imaging, biopsy diagnosis, and treatment times for the highest-risk patients.

Indexed as

Prostatic NeoplasmsTriageAgedHumansMagnetic Resonance ImagingMaleMiddle AgedNeoplasm StagingProstate-Specific AntigenReferral and ConsultationTime-to-TreatmentProstate-Specific Antigenfaster diagnosisinvestigationprostate cancerquality improvementrisk‐stratificationtriage

Identifiers

PMID41744174
PMCPMC13071532

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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.