Evidence map›Paper›PMID 34830914›Full record

ArticleCancers2021

hENT1 Predicts Benefit from Gemcitabine in Pancreatic Cancer but Only with Low CDA mRNA.

Karen Aughton, Nils O Elander, Anthony Evans, Richard Jackson, Fiona Campbell, Eithne Costello, Christopher M Halloran, John R Mackey, Andrew G Scarfe, Juan W Valle and 16 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-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

10 citing papers in PubMed, 12 citations in OpenAlex.

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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

26 authors at 14 institutions in 5 countries.

Karen AughtonLiverpool Experimental Cancer Medicine Centre, 2nd Floor Sherrington Building, Ashton St, University of Liverpool, Liverpool L69 3GE, UK.
Nils O ElanderLiverpool Experimental Cancer Medicine Centre, 2nd Floor Sherrington Building, Ashton St, University of Liverpool, Liverpool L69 3GE, UK.
Anthony EvansLiverpool Experimental Cancer Medicine Centre, 2nd Floor Sherrington Building, Ashton St, University of Liverpool, Liverpool L69 3GE, UK.ORCID 0000-0001-8547-1730
Richard JacksonLiverpool Experimental Cancer Medicine Centre, 2nd Floor Sherrington Building, Ashton St, University of Liverpool, Liverpool L69 3GE, UK.
Fiona CampbellLiverpool Experimental Cancer Medicine Centre, 2nd Floor Sherrington Building, Ashton St, University of Liverpool, Liverpool L69 3GE, UK.
Eithne CostelloLiverpool Experimental Cancer Medicine Centre, 2nd Floor Sherrington Building, Ashton St, University of Liverpool, Liverpool L69 3GE, UK.
Christopher M HalloranLiverpool Experimental Cancer Medicine Centre, 2nd Floor Sherrington Building, Ashton St, University of Liverpool, Liverpool L69 3GE, UK.
John R MackeyCross Cancer Institute, University of Alberta, Edmonton, AB T6G 1Z2, Canada.
Andrew G ScarfeCross Cancer Institute, University of Alberta, Edmonton, AB T6G 1Z2, Canada.
Juan W ValleThe Christie NHS Foundation Trust, University of Manchester, Manchester M20 4BX, UK.ORCID 0000-0002-1999-0863
Ross CarterGlasgow Royal Infirmary, Glasgow G4 0SF, UK.
David CunninghamRoyal Marsden National Health Service (NHS) Foundation Trust, London SW3 6JJ, UK.
Niall C TebbuttAustin Health, Melbourne, VIC 3084, Australia.
David GoldsteinPrince of Wales Hospital and Clinical School, University of New South Wales, Sydney, NSW 2052, Australia.
Jennifer ShannonNepean Cancer Centre, University of Sydney, Sydney, NSW 2747, Australia.
Bengt GlimeliusDepartment of Immunology, Genetics and Pathology, Uppsala University, SE-751 05 Uppsala, Sweden.
Thilo HackertDepartment of Surgery, University of Heidelberg, 69047 Heidelberg, Germany.
Richard M CharnleyFreeman Hospital, Newcastle upon Tyne NE7 7DN, UK.
Alan AnthoneySt James's University Hospital, Leeds LS9 7TF, UK.
Markus M LerchDepartment of Medicine A, University Medicine Greifswald, 17489 Greifswald, Germany.ORCID 0000-0002-9643-8263
Julia MayerleDepartment of Medicine A, University Medicine Greifswald, 17489 Greifswald, Germany.
Daniel H PalmerLiverpool Experimental Cancer Medicine Centre, 2nd Floor Sherrington Building, Ashton St, University of Liverpool, Liverpool L69 3GE, UK.
Markus W BüchlerDepartment of Surgery, University of Heidelberg, 69047 Heidelberg, Germany.
Paula GhanehLiverpool Experimental Cancer Medicine Centre, 2nd Floor Sherrington Building, Ashton St, University of Liverpool, Liverpool L69 3GE, UK.
John P NeoptolemosDepartment of Surgery, University of Heidelberg, 69047 Heidelberg, Germany.
William GreenhalfLiverpool Experimental Cancer Medicine Centre, 2nd Floor Sherrington Building, Ashton St, University of Liverpool, Liverpool L69 3GE, UK.ORCID 0000-0002-1865-3195
University of Liverpool · GBHeidelberg University · DEUniversitätsmedizin Greifswald · DEUniversity of Alberta · CAAustin Health · AUFreeman Hospital · GBGlasgow Royal Infirmary · GBLinköping University · SENational Health Service · GBSt James's University Hospital · GBThe University of Sydney · AUUniversity of Manchester · GBUNSW Sydney · AUUppsala University · SE

Funding

Cancer Research UK 11883Cancer Research UK 15957Cancer Research UK 16186Cancer Research UK 16791Cancer Research UK 16812Cancer Research UK 17680Cancer Research UK 8968Cancer Research UK C18616/A25153
6 · The paper itself

Abstract

Gemcitabine or 5-fluorouracil (5-FU) based treatments can be selected for pancreatic cancer. Equilibrative nucleoside transporter 1 (hENT1) predicts adjuvant gemcitabine treatment benefit over 5-FU. Cytidine deaminase (CDA), inside or outside of the cancer cell, will deaminate gemcitabine, altering transporter affinity. ESPAC-3(v2) was a pancreatic cancer trial comparing adjuvant gemcitabine and 5-FU. Tissue microarray sections underwent in situ hybridization and immunohistochemistry. Analysis of both CDA and hENT1 was possible with 277 patients. The transcript did not correlate with protein levels for either marker. High hENT1 protein was prognostic with gemcitabine; median overall survival was 26.0 v 16.8 months (

Indexed as

5-fluorouracilbiomarkerchemotherapygemcitabinepredictive markerprognostic markerpyrimidine

Identifiers

PMID34830914
PMCPMC8616255
OpenAlexW3213984269

What OpenQuestion holds

Textmetadata
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.