Evidence map›Paper›PMID 33100327›Full record

Trial reportBritish journal of cancer2021

Circulating biomarkers and outcomes from a randomised phase 2 trial of gemcitabine versus capecitabine-based chemoradiotherapy for pancreatic cancer.

Frances Willenbrock, Catrin M Cox, Eileen E Parkes, Charlotte S Wilhelm-Benartzi, Aswin G Abraham, Robert Owens, Ahmad Sabbagh, Christopher M Jones, Daniel L I Hughes, Tim Maughan and 3 more

Open access · hybridAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in British journal of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 26% of its field
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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. The roles of CC chemokines in response to radiation.Radiation oncology (London, England) · 2022
    Review
  7. Article
  8. 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 at 4 institutions in 1 country.

Frances WillenbrockDepartment of Oncology, University of Oxford, Oxford, UK.
Catrin M CoxCentre for Trials Research, Cardiff, UK.
Eileen E ParkesDepartment of Oncology, University of Oxford, Oxford, UK.
Charlotte S Wilhelm-BenartziCentre for Trials Research, Cardiff, UK.
Aswin G AbrahamCross Cancer Institute, Edmonton, AB, Canada.
Robert OwensOxford University Hospital NHS Trust, Oxford, UK.
Ahmad SabbaghWeston Park Cancer Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Christopher M JonesUniversity of Leeds & Leeds Cancer Centre, Leeds, UK.
Daniel L I HughesDepartment of Oncology, University of Oxford, Oxford, UK.
Tim MaughanDepartment of Oncology, University of Oxford, Oxford, UK.
Christopher N Hurt *Centre for Trials Research, Cardiff, UK.ORCID http://orcid.org/0000-0003-1206-8355
Eric E O'Neill *Department of Oncology, University of Oxford, Oxford, UK.
Somnath Mukherjee *Department of Oncology, University of Oxford, Oxford, UK. somnath.mukherjee@oncology.ox.ac.uk.
University of Oxford · GBOxford University Hospitals NHS Trust · GBUniversity of Leeds · GBWeston Park Cancer Centre · GB

Funding

Cancer Research UK 15954Cancer Research UK 25350Wellcome Trust
6 · The paper itself

Abstract

backgroundThe Phase 2 SCALOP trial compared gemcitabine with capecitabine-based consolidation chemoradiotherapy (CRT) in locally advanced pancreatic cancer (LAPC).

methodsThirty-five systematically identified circulating biomarkers were analysed in plasma samples from 60 patients enroled in SCALOP. Each was measured in triplicate at baseline (prior to three cycles of gemcitabine-capecitabine induction chemotherapy) and, for a subset, prior to CRT. Association with overall survival (OS) was determined using univariable Cox regression and optimal thresholds delineating low to high values identified using time-dependent ROC curves. Independence from known prognostic factors was assessed using Spearman correlation and the Wilcoxon rank sum test prior to multivariable Cox regression modelling including independent biomarkers and known prognostic factors.

resultsBaseline circulating levels of C-C motif chemokine ligand 5 (CCL5) were significantly associated with OS, independent of other clinicopathological characteristics. Patients with low circulating CCL5 (CCL5

conclusionsCCL5 is an independent prognostic biomarker in LAPC. Given the known role of CCL5 in tumour invasion, metastasis and the induction of an immunosuppressive micro-environment, targeting of CCL5-mediated pathways may offer therapeutic potential in pancreatic cancer. CLINICAL

trial registrationThe SCALOP trial was registered with ISRCTN, number 96169987 (registered 29 May 2008).

Indexed as

AgedBiomarkers, TumorCapecitabineChemokine CCL5ChemoradiotherapyCytokinesDeoxycytidineFemaleGemcitabineHumansInduction ChemotherapyMaleMiddle AgedPancreatic NeoplasmsRegression AnalysisROC CurveBiomarkers, TumorCapecitabineCCL5 protein, humanChemokine CCL5CytokinesDeoxycytidineGemcitabine

Identifiers

PMID33100327
PMCPMC7851394
OpenAlexW3093504991

What OpenQuestion holds

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LicenceCC BY
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.