Evidence map›Paper›PMID 41201528›Full record

ArticleAnnals of surgical oncology2026

Impact of Different Primary Treatment Strategies on Recurrence-Focused Treatment of Pancreatic Ductal Adenocarcinoma.

Paul C M Andel, Iris W J M van Goor, Thijs J Schouten, Marc G Besselink, Bert A Bonsing, Koop Bosscha, Olivier R Busch, Geert A Cirkel, Ronald M van Dam, Sebastiaan Festen and 20 more

Abstract read
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In one paragraph

Article in Annals of surgical oncology, 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

30 authors.

Paul C M AndelDepartment of Surgery, Regional Academic Cancer Center Utrecht, UMC Utrecht Cancer Center & St Antonius Hospital Nieuwegein, Utrecht, The Netherlands.
Iris W J M van GoorDepartment of Surgery, Regional Academic Cancer Center Utrecht, UMC Utrecht Cancer Center & St Antonius Hospital Nieuwegein, Utrecht, The Netherlands.
Thijs J SchoutenDepartment of Surgery, Regional Academic Cancer Center Utrecht, UMC Utrecht Cancer Center & St Antonius Hospital Nieuwegein, Utrecht, The Netherlands.
Marc G BesselinkDepartment of Surgery, Amsterdam UMC, location University of Amsterdam, Amsterdam, The Netherlands.
Bert A BonsingDepartment of Surgery, Leiden University Medical Center, Leiden, The Netherlands.
Koop BosschaDepartment of Surgery, Jeroen Bosch Hospital, Den Bosch, The Netherlands.
Olivier R BuschDepartment of Surgery, Amsterdam UMC, location University of Amsterdam, Amsterdam, The Netherlands.
Geert A CirkelDepartment of Medical Oncology, University Medical Center Utrecht Cancer Center & Meander Medical Center Amersfoort, Regional Academic Cancer Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Ronald M van DamDepartment of Surgery, Maastricht UMC+, Maastricht, The Netherlands.
Sebastiaan FestenDepartment of Surgery, OLVG, Amsterdam, The Netherlands.
Bas Groot KoerkampDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Erwin van der HarstDepartment of Surgery, Maasstad Hospital, Rotterdam, The Netherlands.
Ignace H J T de HinghDepartment of Surgery, Catharina Hospital, Eindhoven, The Netherlands.
Martijn P W IntvenDepartment of Radiation Oncology, University Medical Center Utrecht Cancer Center, Utrecht, The Netherlands.
Geert KazemierCancer Center Amsterdam, Amsterdam, The Netherlands.
Mike S L LiemDepartment of Surgery, Medisch Spectrum Twente, Enschede, The Netherlands.
Maartje LosDepartment of Medical Oncology, Regional Academic Cancer Center Utrecht, Utrecht University, University Medical Center Utrecht Cancer Center, Utrecht, The Netherlands.
Gert MeijerDepartment of Radiation Oncology, University Medical Center Utrecht Cancer Center, Utrecht, The Netherlands.
Vincent E de MeijerDepartment of Surgery, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Vincent B NieuwenhuijsDepartment of Surgery, Isala, Zwolle, The Netherlands.
Daphne RoosDepartment of Surgery, Renier de Graaf Gasthuis, Delft, The Netherlands.
Jennifer M J SchreinemakersDepartment of Surgery, Amphia Hospital, Breda, The Netherlands.
Martijn W J StommelDepartment of Surgery, Radboud University Medical Center, Nijmegen, The Netherlands.
Fennie WitDepartment of Surgery, Tjongerschans Hospital, Heerenveen, The Netherlands.
Robert C VerdonkDepartment of Gastroenterology, Regional Academic Cancer Center Utrecht, Utrecht, The Netherlands.
Hjalmar C van SantvoortDepartment of Surgery, Regional Academic Cancer Center Utrecht, UMC Utrecht Cancer Center & St Antonius Hospital Nieuwegein, Utrecht, The Netherlands.
I Quintus MolenaarDepartment of Surgery, Regional Academic Cancer Center Utrecht, UMC Utrecht Cancer Center & St Antonius Hospital Nieuwegein, Utrecht, The Netherlands.
Lois A DaamenDepartment of Surgery, Regional Academic Cancer Center Utrecht, UMC Utrecht Cancer Center & St Antonius Hospital Nieuwegein, Utrecht, The Netherlands.
Vincent P GrootDepartment of Surgery, Regional Academic Cancer Center Utrecht, UMC Utrecht Cancer Center & St Antonius Hospital Nieuwegein, Utrecht, The Netherlands. v.p.groot@umcutrecht.nl.
Dutch Pancreatic Cancer Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIncreased application of neoadjuvant therapy (NAT) and adjuvant therapy (AT) could limit treatment options for pancreatic ductal adenocarcinoma (PDAC) recurrence. This study aimed to identify patterns of recurrence-focused treatment and survival following different primary treatment strategies.

methodsAll patients who underwent PDAC resection in the Netherlands (2014-2019) were included. Patients were divided into five groups according to their primary treatment strategy: (1) resection only, (2) gemcitabine-based NAT + resection, (3) FOLFIRINOX-based NAT + resection, (4) resection + gemcitabine-based AT, and (5) resection + FOLFIRINOX-based AT. Differences in recurrence-focused treatment and post-recurrence survival (PRS) were assessed using multivariable logistic and Cox-proportional hazards analyses and were presented as odds ratios (ORs) and hazard ratios (HRs) with corresponding 95% confidence intervals (95% CIs), respectively.

resultsIn total, 1739 patients (median follow-up of 51 [interquartile range 34-64] months) were included, of whom 1272 (73%) had disease recurrence. In these patients, recurrence-focused treatment was administered in 64/124 (52%) after FOLFIRINOX-based NAT compared with 74/410 (18%) with resection only (OR 4.13 [95% CI 3.34-5.12]; P<0.001), 29/70 (41%) with gemcitabine-based NAT (OR 1.61 [95% CI 1.21-2.15]; P<0.001), 239/604 (39%) with gemcitabine-based AT (OR 1.73 [95% CI 1.43-2.09]; P<0.001), and 24/64 (38%) with FOLFIRINOX-based AT (OR 1.44 [95% CI 1.06-1.95]; P=0.02). Recurrence-focused treatment was associated with a median PRS of 11 (95% CI 10-13) months compared with 3 (95% CI 2-3) months in patients with best supportive care (HR 0.31 [95% CI 0.26-0.37]; P<0.001).

conclusionsRecurrence-focused treatment differs between patients with PDAC who received different primary treatment strategies and is associated with improved PRS.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalNeoadjuvant TherapyNeoplasm Recurrence, LocalPancreatectomyPancreatic NeoplasmsAgedChemotherapy, AdjuvantDeoxycytidineFemaleFluorouracilFollow-Up StudiesGemcitabineHumansIrinotecanLeucovorinDeoxycytidineFluorouracilfolfirinoxGemcitabineIrinotecanLeucovorinOxaliplatinCancer recurrencePancreatic cancerPancreatic resectionRecurrence treatmentSurvival

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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.