Evidence map›Paper›PMID 39924679›Full record

ArticleFuture oncology (London, England)2025

Predictive factors of FOLFIRINOX chemotherapy toxicity in pancreatic adenocarcinoma patients.

Roland Eid, Anthony Tarabay, Pierre Decazes, Clémence David, Fouad Kerbage, Jean Zeghondy, Leony Antoun, Cristina Smolenschi, Alina Fuerea, Marine Valery and 10 more

Abstract read
In one paragraph

Article in Future oncology (London, England), 2025. 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

20 authors.

Roland EidDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.ORCID 0000-0003-1097-2594
Anthony TarabayDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Pierre DecazesDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Clémence DavidDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Fouad KerbageDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Jean ZeghondyDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Leony AntounDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Cristina SmolenschiDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Alina FuereaDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Marine ValeryDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Valerie BoigeDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Maximiliano GelliDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Lambros TselikasDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Jerome Durand-LabrunieDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Younes BelkouchiDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Lawrance LittishaDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Samy AmmariDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Michel DucreuxDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Nathalie LassauDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
Antoine HollebecqueDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFOLFIRINOX, a primary chemotherapy for metastatic pancreatic cancer, often causes severe toxicity, necessitating hospitalization and dose adjustments. This study aims to identify predictors of FOLFIRINOX toxicity, focusing on biological, clinical, and anthropometric factors. MATERIAL &

methodsThis retrospective study analyzes pancreatic adenocarcinoma patients on FOLFIRINOX, assessing pre-treatment biological, clinical, and anthropometric traits. Hospitalizations and tolerance during the first chemotherapy month were evaluated using CTCAE v5.0 grading, with early toxicity assessed via anthropometric factors using Anthropometer3DNet software from pre-treatment scans.

resultsIn 152 pancreatic cancer patients (median age: 62), FOLFIRINOX was administered in metastatic (81%), locally advanced (14%), and adjuvant/neoadjuvant (5%) settings. Performance Status was zero (49%), one (41%) and ≥ 2 (10%). Median follow-up was 62.5 months, with median overall survival of 13.7 months and progression-free survival of 8.9 months. First-cycle dose reduction occurred in 14% of patients. Within the first month, 48% experienced toxicity leading to hospitalization and/or dose reduction, with 28% requiring a median 8-day hospitalization. Low muscle body mass (MBM) significantly correlated with dose reduction (AUC 0.63;

conclusionLow MBM is linked to FOLFIRINOX toxicity, suggesting MBM assessment could allow better selection of patients to avoid these toxicities, warranting further confirmation in larger cohorts.

Indexed as

AdenocarcinomaAntineoplastic Combined Chemotherapy ProtocolsPancreatic NeoplasmsAdultAgedAged, 80 and overFemaleFluorouracilHumansIrinotecanLeucovorinMaleMiddle AgedOxaliplatinPrognosisRetrospective StudiesFluorouracilfolfirinoxIrinotecanLeucovorinOxaliplatinanthropometricFOLFIRINOXPancreatic adenocarcinomasurvivaltoxicity

Identifiers

PMID39924679
PMCPMC11881864

What OpenQuestion holds

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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.