Evidence map›Paper›PMID 41741817›Full record

ArticleBritish journal of cancer2026

Real-world outcomes following adjuvant chemotherapy for resected pancreatic cancer in a centralised oncology service.

Jessica Hale, Timothy Gilbert, Martyn Stott, Philip Whelan, Richard Jackson, Helen Wong, Marie McKay, Paula Ghaneh, Christopher Halloran, Olusola Faluyi and 3 more

Abstract read
In one paragraph

Article in British journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Jessica Hale *The Clatterbridge Cancer Centre, Liverpool, UK.
Timothy Gilbert *Department of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Martyn StottDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Philip WhelanLiverpool University Hospitals NHS Foundation Trust, Liverpool, UK.
Richard JacksonLiverpool Clinical Trials Centre, University of Liverpool, Liverpool, UK.
Helen WongThe Clatterbridge Cancer Centre, Liverpool, UK.
Marie McKayThe Clatterbridge Cancer Centre, Liverpool, UK.
Paula GhanehDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Christopher HalloranDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.ORCID http://orcid.org/0000-0002-5471-4178
Olusola FaluyiThe Clatterbridge Cancer Centre, Liverpool, UK.
Declan DunneDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
John P NeoptolemosDepartment of General, Visceral and Transplantation Surgery, Heidelberg University Hospital, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-6201-7399
Daniel PalmerThe Clatterbridge Cancer Centre, Liverpool, UK. Palmerd@liverpool.ac.uk.ORCID http://orcid.org/0000-0002-7147-5703

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic cancer remains a significant challenge to diagnose and treat, with considerable regional variation in management and outcomes. This study aimed to evaluate real-world outcomes of patients receiving adjuvant treatment for pancreatic cancer at a single centre in Northwest England over an 11-year period.

methodsData were collected retrospectively on all patients who underwent surgery for pancreatic ductal adenocarcinoma between 2009 and 2020. Collected data included patient demographics, surgical details and adjuvant treatment received, including number of chemotherapy cycles and dose reductions.

results30-day/inpatient mortality was low (2.4%). Adjuvant chemotherapy delivery rates were high (82%) with 67.4% of patients completing the intended number of cycles. There was no additional survival benefit for patients who started chemotherapy within 8 weeks post-surgery compared to those who began later. Dose reductions did not impact survival, provided patients completed the full course of treatment (mOS 27.5 months vs. 28.5 months; HR 1.14, 95% CI 0.76-1.70 p = 0.513). Following centralisation of care, a greater proportion of patients commenced adjuvant treatment (86% vs 69% p < 0.05).

conclusionA high proportion of patients received adjuvant treatment, with a centralised clinic model leading to increased rates of adjuvant chemotherapy delivery. Completion of the full chemotherapy course was more critical than dose intensity. Larger prospective studies are needed to investigate the factors contributing to regional variations.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalPancreatic NeoplasmsAgedAged, 80 and overChemotherapy, AdjuvantFemaleHumansMaleMiddle AgedPancreatectomyRetrospective StudiesTreatment Outcome

Identifiers

PMID41741817
PMCPMC13036073

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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.