Evidence map›Paper›PMID 28129987›Full record

Trial reportLancet (London, England)2017

Comparison of adjuvant gemcitabine and capecitabine with gemcitabine monotherapy in patients with resected pancreatic cancer (ESPAC-4): a multicentre, open-label, randomised, phase 3 trial.

John P Neoptolemos, Daniel H Palmer, Paula Ghaneh, Eftychia E Psarelli, Juan W Valle, Christopher M Halloran, Olusola Faluyi, Derek A O'Reilly, David Cunningham, Jonathan Wadsley and 25 more

4 registry-linked trialsOpen access · bronzeAbstract readClinical Trial, Phase IIIComparative StudyMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Lancet (London, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 957 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
957citing papers in PubMed, 9 pooled it
94.3field-weighted citation impact, top 1% 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.

NCT03959150 phase2 / phase3unknown statusnot on this mapstarted 2020, after this paper: background citation

A Multi-center, II Phase,Randomized Controlled Clinical Study of Capecitabine Metronomic Chemotherapy After Gemcitabine Plus Capecitabine Standard Adjuvant Therapy for Stage II/III Pancreatic Cancer

TypeinterventionalSponsorRuijin HospitalRan2020 to 2023Enrolled231ConditionsPancreatic CancerArmsCapecitabine
NCT04893408 completednot on this map

Postoperative and Long-term Survival in Relation to Life-expectancy After Pancreatic Surgery in Elderly Patients

TypeobservationalSponsorRigshospitalet, DenmarkRan2010 to 2019Enrolled1,556ConditionsPancreatic CancerArmsobservational study
NCT05595811 completednot on this map

The Outcome After Operation for Pancreatic and Periampullary Tumors in Greeland Inuit.

TypeobservationalSponsorRigshospitalet, DenmarkRan1999 to 2021Enrolled2,326ConditionsPancreatic Neoplasms, Periampullary NeoplasmsArmsoutcome following surgery
NCT06574620 narecruitingnot on this mapstarted 2025, after this paper: background citation

Accelerating the Actionability of Treatment in Resected and Locally Advanced Pancreatic Cancer

TypeinterventionalSponsorBritish Columbia Cancer AgencyRan2025 to 2031Enrolled200ConditionsPancreatic Ductal Adenocarcinoma, Resectable Pancreatic Ductal Adenocarcinoma, Borderline Resectable Pancreatic Ductal Adenocarcinoma, Locally Advanced Pancreatic Ductal AdenocarcinomaArmsGenetic testing, Optional biopsy, Tissue collection
3 · Its place in the literature

Who cites it

957 citing papers in PubMed, 9 syntheses or guidelines pooled it, 1,902 citations in OpenAlex.

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  7. Chemotherapy and radiotherapy for advanced pancreatic cancer.The Cochrane database of systematic reviews · 2024
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897 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

35 authors at 20 institutions in 4 countries.

John P NeoptolemosUniversity of Liverpool, Liverpool, UK; The Royal Liverpool University Hospital, Liverpool, UK. Electronic address: j.p.neoptolemos@liverpool.ac.uk.
Daniel H PalmerUniversity of Liverpool, Liverpool, UK; The Clatterbridge Cancer Centre, Wirral, UK.
Paula GhanehThe Royal Liverpool University Hospital, Liverpool, UK.
Eftychia E PsarelliUniversity of Liverpool, Liverpool, UK.
Juan W ValleUniversity of Manchester/The Christie NHS Foundation Trust, Manchester, UK.
Christopher M HalloranUniversity of Liverpool, Liverpool, UK; The Royal Liverpool University Hospital, Liverpool, UK.
Olusola FaluyiThe Clatterbridge Cancer Centre, Wirral, UK.
Derek A O'ReillyManchester Royal Infirmary, Manchester, UK.
David CunninghamRoyal Marsden Hospital, London, UK.
Jonathan WadsleyWeston Park Hospital, Sheffield, UK.
Suzanne DarbyWeston Park Hospital, Sheffield, UK.
Tim MeyerRoyal Free Hospital, London, UK.
Roopinder GillmoreRoyal Free Hospital, London, UK.
Alan AnthoneySt James's University Hospital, Leeds, UK.
Pehr LindKarolinska Institute, Stockholm, Sweden; Clinical Research Sörmland, Eskilstuna, Sweden.
Bengt GlimeliusUniversity of Uppsala, Uppsala, Sweden.
Stephen FalkBristol Haematology and Oncology Centre, Bristol, UK.
Jakob R IzbickiUniversity of Hamburg Medical institutions UKE, Hamburg, Germany.
Gary William MiddletonRoyal Surrey County Hospital, Guildford, UK.
Sebastian CumminsRoyal Surrey County Hospital, Guildford, UK.
Paul J RossGuy's Hospital, London, UK.
Harpreet WasanHammersmith Hospital, London, UK.
Alec McDonaldThe Beatson West of Scotland Cancer Centre, Glasgow, UK.
Tom CrosbyVelindre Hospital, Cardiff, UK.
Yuk Ting MaQueen Elizabeth Hospital, Birmingham, UK.
Kinnari PatelChurchill Hospital, Oxford, UK.
David SherriffDerriford Hospital, Plymouth, UK.
Rubin SoomalIpswich Hospital, Ipswich, UK.
David BorgSkåne University Hospital, Lund, Sweden.
Sharmila SothiUniversity Hospital Coventry, Coventry, UK.
Pascal HammelHôpital Beaujon, Clichy, France.
Thilo HackertUniversity of Heidelberg, Germany.
Richard JacksonUniversity of Liverpool, Liverpool, UK.
Markus W BüchlerUniversity of Heidelberg, Germany.
European Study Group for Pancreatic Cancer
University of Liverpool · GBHeidelberg University · DERoyal Surrey County Hospital · GBThe Royal Free Hospital · GBWeston Park Cancer Centre · GBAt Bristol · GBBeatson West of Scotland Cancer Centre · GBChurchill Hospital · GBClatterbridge Cancer Centre NHS Foundation Trust · GBDerriford Hospital · GBGuy's Hospital · GBHammersmith Hospital · GBHôpital Beaujon · FRIpswich Hospital · GBKarolinska Institutet · SEManchester Royal Infirmary · GBQueen Elizabeth Hospital Birmingham · GBRoyal Marsden Hospital · GBSkåne University Hospital · SESt James's University Hospital · GB

Funding

Cancer Research UK 11883Cancer Research UK 15957Cancer Research UK 16186Cancer Research UK 16791Cancer Research UK 17680Cancer Research UK 8968Department of Health 08/29/02
6 · The paper itself

Abstract

backgroundThe ESPAC-3 trial showed that adjuvant gemcitabine is the standard of care based on similar survival to and less toxicity than adjuvant 5-fluorouracil/folinic acid in patients with resected pancreatic cancer. Other clinical trials have shown better survival and tumour response with gemcitabine and capecitabine than with gemcitabine alone in advanced or metastatic pancreatic cancer. We aimed to determine the efficacy and safety of gemcitabine and capecitabine compared with gemcitabine monotherapy for resected pancreatic cancer.

methodsWe did a phase 3, two-group, open-label, multicentre, randomised clinical trial at 92 hospitals in England, Scotland, Wales, Germany, France, and Sweden. Eligible patients were aged 18 years or older and had undergone complete macroscopic resection for ductal adenocarcinoma of the pancreas (R0 or R1 resection). We randomly assigned patients (1:1) within 12 weeks of surgery to receive six cycles of either 1000 mg/m

findingsOf 732 patients enrolled, 730 were included in the final analysis. Of these, 366 were randomly assigned to receive gemcitabine and 364 to gemcitabine plus capecitabine. The Independent Data and Safety Monitoring Committee requested reporting of the results after there were 458 (95%) of a target of 480 deaths. The median overall survival for patients in the gemcitabine plus capecitabine group was 28·0 months (95% CI 23·5-31·5) compared with 25·5 months (22·7-27·9) in the gemcitabine group (hazard ratio 0·82 [95% CI 0·68-0·98], p=0·032). 608 grade 3-4 adverse events were reported by 226 of 359 patients in the gemcitabine plus capecitabine group compared with 481 grade 3-4 adverse events in 196 of 366 patients in the gemcitabine group.

interpretationThe adjuvant combination of gemcitabine and capecitabine should be the new standard of care following resection for pancreatic ductal adenocarcinoma.

fundingCancer Research UK.

Indexed as

AdultAgedAged, 80 and overAntimetabolites, AntineoplasticAntineoplastic Combined Chemotherapy ProtocolsCapecitabineCarcinoma, Pancreatic DuctalChemotherapy, AdjuvantDeoxycytidineFemaleGemcitabineHumansKaplan-Meier EstimateMaleMiddle AgedPancreatic NeoplasmsAntimetabolites, AntineoplasticCapecitabineDeoxycytidineGemcitabine

Identifiers

PMID28129987
OpenAlexW2581973599

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.