Evidence map›Paper›PMID 42384236›Full record

Trial reportLangenbeck's archives of surgery2026

Longitudinal assessment of health-related quality of life in patients with borderline and locally advanced pancreatic cancer undergoing neoadjuvant FOLFIRINOX chemotherapy: results from a prospective multicenter trial.

Luís Filipe Abreu de Carvalho, Wim Ceelen, Annick Meertens, Niki Rashidian, Bruno Waked, Karen Geboes, Suzane Ribeiro, Koen Gorleer, Hans Dedecker, Lars Triest and 8 more

Registry-linked trialAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Langenbeck's archives of surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05298722 (Prediction of Surgical Resectability After FOLFIRINOX Chemotherapy for Borderline Resectable and Locally Advanced Pancreatic Cancer), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

NCT05298722 narecruitingnot on this map

Prediction of Surgical Resectability After FOLFIRINOX Chemotherapy for Borderline Resectable and Locally Advanced Pancreatic Cancer: the Role of Diffusion Weighted Magnetic Resonance Imaging, Radiomics and Liquid Biopsy

TypeinterventionalSponsorUniversity Hospital, GhentRan2022 to 2028Enrolled45ConditionsPancreatic CancerArmsImaging analysis of CT-scan and MRI with radiomics and genetic analysis of peripheral blood samples and questionnaires.
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Luís Filipe Abreu de CarvalhoDepartment of HPB surgery and liver transplantation, Ghent University Hospital, Corneel Heymanslaan 10 , Ghent, 9000, Belgium. Luis.AbreudeCarvalho@UZGent.be.ORCID http://orcid.org/0000-0001-5821-5512
Wim CeelenDepartment of Gastrointestinal surgery, Ghent University Hospital, Ghent, Belgium.
Annick MeertensDepartment of Dermatology, University Hospital Ghent, Ghent, Belgium.
Niki RashidianDepartment of HPB surgery and liver transplantation, Ghent University Hospital, Corneel Heymanslaan 10 , Ghent, 9000, Belgium.
Bruno WakedDepartment of Gastroenterology, Division of Digestive Oncology, Ghent Sint-Lucas hospital, Ghent, Belgium.
Karen GeboesDepartment of Gastroenterology, Division of Digestive Oncology, Ghent University Hospital, Ghent, Belgium.
Suzane RibeiroDepartment of Gastroenterology, Division of Endoscopy and Digestive Oncology, Ghent University Hospital, Ghent, Belgium.
Koen GorleerDepartment of Gastroenterology, Division of Digestive Oncology, VITAZ hospital, Sint-Niklaas, Belgium.
Hans DedeckerDepartment of Gastroenterology, Division of Digestive Oncology, VITAZ hospital, Sint-Niklaas, Belgium.
Lars TriestDepartment of Gastroenterology, Division of Digestive Oncology, Sint-Blasius hospital, Dendermonde, Belgium.
Andrew VervaeckeDepartment of Gastroenterology, Zeno Hospital, Knokke-Heist and Blankenberge, Belgium.
Steven SasDepartment of Gastroenterology, Division of Digestive Oncology, Jan Palfijn Hospital, Ghent, Belgium.
Bart SierensDepartment of Gastroenterology, Division of Digestive Oncology, Eeklo Hospital AZ ALMA, Eeklo, Belgium.
Carolien BeylsDepartment of Gastroenterology, Division of Digestive Oncology, Oudenaarde Hospital, Oudenaarde, Belgium.
Mark SieDepartment of Medical Oncology, Division of Digestive Oncology, Zorgsaam hospital, Terneuzen, The Netherlands.
Marjan van DijkDepartment of Medical Oncology, Division of Digestive Oncology, Zorgsaam hospital, Terneuzen, The Netherlands.
Nick VerhaegheDepartment of Public Health and Primary Care, Interuniversity Centre for Health Economics Research (I-CHER), Ghent University, Ghent, Belgium.
Frederik BerrevoetDepartment of HPB surgery and liver transplantation, Ghent University Hospital, Corneel Heymanslaan 10 , Ghent, 9000, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePancreatic ductal adenocarcinoma (PDAC) carries a poor prognosis and significantly affects health-related quality of life (HRQoL). In borderline resectable (BR) and locally advanced (LA) PDAC, neoadjuvant FOLFIRINOX may enable surgical resection, but its toxicity can further compromise HRQoL. Evidence on longitudinal HRQoL changes during FOLFIRINOX in this context remains limited. This study evaluated HRQoL trajectories in patients with BR and LA PDAC receiving neoadjuvant chemotherapy (NACT) within a surgical selection strategy.

methodsThis longitudinal analysis included patients from the multicenter prospective PeRFormanCe trial (NCT05298722), investigating outcomes in BR and LA PDAC treated with FOLFIRINOX as NACT. HRQoL was assessed at baseline and after 4, 8, and 12 NACT cycles using EORTC QLQ-C30 and PAN26 questionnaires. Changes over time were analyzed using linear mixed-effect models. Clinically meaningful differences were defined as ≥10-point mean changes with 95% confidence intervals.

resultsTwenty patients were included (35% female), 12 (60%) had LA PDAC. The median number of NACT cycles was 8 (IQR 7-12). Sixteen patients (80%) underwent surgical exploration, and 11 (55%) achieved resection. During NACT, patients reported improvements in insomnia, pain, hepatic symptoms, bloating and appetite loss. Muscle weakness, cognitive deterioration, and side effects increased. Among patients completing 12 cycles, weight loss and flatulence decreased, global health status (baseline 64, SE 4.05) and fatigue scores improved.

conclusionIn patients with BR and LA PDAC treated with FOLFIRINOX as NACT, HRQoL can be preserved over time despite variations in symptoms. These findings contribute to informed, patient-centered decision-making in the neoadjuvant setting.

trial registrationClinicalTrials.gov Identifier NCT05298722. Date of registration March 28, 2022.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalNeoadjuvant TherapyPancreatic NeoplasmsQuality of LifeAgedFemaleFluorouracilHumansIrinotecanLeucovorinLongitudinal StudiesMaleMiddle AgedOxaliplatinProspective StudiesFluorouracilfolfirinoxIrinotecanLeucovorinOxaliplatinBorderline resectable pancreatic cancerFOLFIRINOXHealth-related quality of lifeLocally advanced pancreatic cancerNeoadjuvant chemotherapyPancreatic cancer

Identifiers

PMID42384236
PMCPMC13593662

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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.