Evidence map›Paper›PMID 37550634›Full record

ArticleBMC cancer2023

Perioperative or adjuvant mFOLFIRINOX for resectable pancreatic cancer (PREOPANC-3): study protocol for a multicenter randomized controlled trial.

J L van Dam, E M M Verkolf, E N Dekker, B A Bonsing, S O Bratlie, L A A Brosens, O R Busch, L M J W van Driel, C H J van Eijck, S Feshtali and 22 more

2 registry-linked trialsOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 46 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 6 pooled it
11.3field-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.

NCT04927780 phase3active not recruitingnot on this map

Perioperative Versus Adjuvant FOLFIRINOX for Resectable Pancreatic Cancer: the PREOPANC-3 Study

TypeinterventionalSponsorErasmus Medical CenterRan2021 to 2029Enrolled378ConditionsPancreatic Cancer, Pancreatic Ductal Adenocarcinoma, Resectable Pancreatic AdenocarcinomaArmsLeucovorin Calcium, Fluorouracil, Irinotecan Hydrochloride, Oxaliplatin, Resection
NCT07081360 phase3recruitingnot on this mapstarted 2025, after this paper: background citation

Neoadjuvant Chemotherapy Followed by Surgery Versus Upfront Surgery for Clearly Resectable Pancreatic Head Cancer and Periampullary Cancer: A Randomized Controlled Trial

TypeinterventionalSponsorMinia UniversityRan2025 to 2028Enrolled262ConditionsPancreas Cancer, Periampullary Cancer, Periampullary Carcinoma Resectable, Pancreatic Cancer ResectableArmsNeoadjuvant chemotherapy, Upfront Surgery Group
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 6 syntheses or guidelines pooled it, 50 citations in OpenAlex.

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  15. Pancreatic cancer.Nature reviews. Disease primers · 2026
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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

32 authors at 20 institutions in 3 countries.

J L van DamDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
E M M VerkolfDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
E N DekkerDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
B A BonsingDepartment of Surgery, Leiden University Medical Center, Leiden, The Netherlands.
S O BratlieDepartment of Surgery, Sahlgrenska University Hospital, Gothenburg, Sweden.
L A A BrosensDepartment of Pathology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
O R BuschDepartment of Surgery, Amsterdam UMC, Location University of Amsterdam, Amsterdam, The Netherlands.
L M J W van DrielDepartment of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
C H J van EijckDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
S FeshtaliDepartment of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
P GhorbaniDivision of Surgery, Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden.
D J A de GrootDepartment of Medical Oncology, University Medical Center Groningen, Groningen, The Netherlands.
J W B de GrootDepartment of Medical Oncology, Isala Oncology Center, Zwolle, The Netherlands.
B C M HaberkornDepartment of Medical Oncology, Maasstad Hospital, Rotterdam, The Netherlands.
I H de HinghDepartment of Surgery, Catharina Hospital, Eindhoven, The Netherlands.
B van der HoltDepartment of Hematology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
T M KarstenDepartment of Surgery, OLVG, Amsterdam, The Netherlands.
M B van der KolkDepartment of Surgery, Radboud University Medical Center, Nijmegen, The Netherlands.
K J LaboriDepartment of Hepato-Pancreato-Biliary Surgery, Oslo University Hospital, Rikshospitalet and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
M S L LiemDepartment of Surgery, Medisch Spectrum Twente, Enschede, The Netherlands.
O J L LoosveldDepartment of Medical Oncology, Amphia Hospital, Breda, The Netherlands.
I Q MolenaarDepartment of Surgery, Regional Academic Cancer Center Utrecht, St. Antonius Hospital and University Medical Center Utrecht, Utrecht, The Netherlands.
M B PoléeDepartment of Medical Oncology, Medical Center Leeuwarden, Leeuwarden, The Netherlands.
H C van SantvoortDepartment of Surgery, Regional Academic Cancer Center Utrecht, St. Antonius Hospital and University Medical Center Utrecht, Utrecht, The Netherlands.
J de Vos-GeelenDivision of Medical Oncology, Department of Internal Medicine, GROW, Maastricht UMC+, Maastricht, the Netherlands.
M L WumkesDepartment of Medical Oncology, Jeroen Bosch Hospital, Den Bosch, The Netherlands.
G van TienhovenCancer Center Amsterdam, Amsterdam, The Netherlands.
M Y V HomsDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
M G BesselinkDepartment of Surgery, Amsterdam UMC, Location University of Amsterdam, Amsterdam, The Netherlands.
J W WilminkCancer Center Amsterdam, Amsterdam, The Netherlands.
B Groot KoerkampDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands. b.grootkoerkamp@erasmusmc.nl.
Dutch Pancreatic Cancer Group
Erasmus MC Cancer Institute · NLUniversity of Amsterdam · NLLeiden University Medical Center · NLAmphia Ziekenhuis · NLCancer Center AmsterdamCatharina Ziekenhuis · NLIsala · NLJeroen Bosch Ziekenhuis · NLKarolinska Institutet · SEMaasstad Ziekenhuis · NLMaastricht University Medical Centre · NLMedisch Centrum Leeuwarden · NLMedisch Spectrum Twente · NLOLVG · NLRadboud University Medical Center · NLSahlgrenska University Hospital · SESt. Antonius Ziekenhuis · NLUniversity Medical Center Groningen · NLUniversity Medical Center Utrecht · NLUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSurgical resection followed by adjuvant mFOLFIRINOX (5-fluorouracil with leucovorin, irinotecan, and oxaliplatin) is currently the standard of care for patients with resectable pancreatic cancer. The main concern regarding adjuvant chemotherapy is that only half of patients actually receive adjuvant treatment. Neoadjuvant chemotherapy, on the other hand, guarantees early systemic treatment and may increase chemotherapy use and thereby improve overall survival. Furthermore, it may prevent futile surgery in patients with rapidly progressive disease. However, some argue that neoadjuvant therapy delays surgery, which could lead to progression towards unresectable disease and thus offset the potential benefits. Comparison of perioperative (i.e., neoadjuvant and adjuvant) with (only) adjuvant administration of mFOLFIRINOX in a randomized controlled trial (RCT) is needed to determine the optimal approach.

methodsThis multicenter, phase 3, RCT will include 378 patients with resectable pancreatic ductal adenocarcinoma with a WHO performance status of 0 or 1. Patients are recruited from 20 Dutch centers and three centers in Norway and Sweden. Resectable pancreatic cancer is defined as no arterial contact and ≤ 90 degrees venous contact. Patients in the intervention arm are scheduled for 8 cycles of neoadjuvant mFOLFIRINOX followed by surgery and 4 cycles of adjuvant mFOLFIRINOX (2-week cycle of oxaliplatin 85 mg/m DISCUSSION: The multicenter PREOPANC-3 trial compares perioperative mFOLFIRINOX with adjuvant mFOLFIRINOX in patients with resectable pancreatic cancer.

trial registrationClinical Trials: NCT04927780. Registered June 16, 2021.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsPancreatic NeoplasmsAdjuvants, ImmunologicChemotherapy, AdjuvantFluorouracilHumansIrinotecanLeucovorinMulticenter Studies as TopicNeoadjuvant TherapyOxaliplatinRandomized Controlled Trials as TopicAdjuvants, ImmunologicFluorouracilIrinotecanLeucovorinOxaliplatinAdjuvant therapymFOLFIRINOXNeoadjuvant therapyOverall survivalPancreatic cancerRandomized controlled trial

Identifiers

PMID37550634
PMCPMC10405377
OpenAlexW4385628554

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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.