Evidence map›Paper›PMID 41397201›Full record

ArticleJCO oncology practice2026

Factors Associated With Toxicity of FOLFIRINOX in Elderly Patients With Pancreatic Ductal Adenocarcinoma.

Berenice Collineau, Cecile Bannier-Braticevic, Julia Gilhodes, Céline Delaunay, Elika Loir, Louis Tassy, Philippe Rochigneux, Damien Bruyat, Franck Espinosa, Christophe Manceau and 3 more

Abstract read
In one paragraph

Article in JCO oncology practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

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

13 authors.

Berenice CollineauMedical Oncology Department, Institut Paoli-Calmettes, Marseille, France.ORCID 0000-0002-4009-5871
Cecile Bannier-BraticevicMedical Oncology Department, Institut Paoli-Calmettes, Marseille, France.
Julia GilhodesBiostatistics Department, Institut Paoli-Calmettes, Marseille, France.
Céline DelaunayMedical Oncology Department, Institut Paoli-Calmettes, Marseille, France.
Elika LoirMedical Oncology Department, Institut Paoli-Calmettes, Marseille, France.
Louis TassyMedical Oncology Department, Institut Paoli-Calmettes, Marseille, France.
Philippe RochigneuxMedical Oncology Department, Institut Paoli-Calmettes, Marseille, France.ORCID 0000-0001-7932-0530
Damien BruyatMedical Oncology Department, Institut Paoli-Calmettes, Marseille, France.
Franck EspinosaImaging Department, Institut Paoli-Calmettes, Marseille, France.ORCID 0009-0009-2533-7551
Christophe ManceauImaging Department, Institut Paoli-Calmettes, Marseille, France.
Christelle de la FouchardièreMedical Oncology Department, Institut Paoli-Calmettes, Marseille, France.ORCID 0000-0003-2291-5693
Emmanuel MitryMedical Oncology Department, Institut Paoli-Calmettes, Marseille, France.
Brice ChanezMedical Oncology Department, Institut Paoli-Calmettes, Marseille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeFor elderly patients with pancreatic ductal adenocarcinoma (PDAC), FOLFIRINOX (FFX) is often contraindicated due to frequent grade III adverse events (AEs) limiting available data on this population. MATERIALS AND

methodsThis retrospective single-center study identified patients older than70 years treated with FFX for PDAC (2011-2022). Tumor, G8 score calculation (score <14/17 indicates geriatric examination), geriatric, and nutritional parameters were collected. The primary end point was toxicity, defined as grade ≥3 GI AEs or unplanned hospitalization. Overall survival (OS) and toxicity associated factors were analyzed using Cox regression with stepwise selection.

resultsWe included 142 patients: 73 with metastatic PDAC (mPDAC) and 69 with non-mPDAC (nmPDAC). Median age was 74 years (71-84), with 43% age 75 years and older. 80% had Eastern Cooperative Oncology Group 0-1. G8 score ≤14 and severe malnutrition were more frequent in mPDAC (82% and 51%) than in nmPDAC (64% and 27%). Low muscle mass was present in >80% of cases. Median FFX exposure was four cycles in mPDAC and 4.5 in nmPDAC. Overall, 56% experienced toxicity, including two treatment-related deaths. Frequent grade ≥3 AEs included infections (26%), nausea/vomiting (22%), and diarrhea (18%). Early toxicity within 2 months was associated with worse OS. Factors linked to toxicity included metastatic status (hazard ratio [HR], 2.41) and psychiatric comorbidities (HR, 6.96), while cardiovascular disease (HR, 0.35) and history of cancer (HR, 0.22) were protective. In nmPDAC, multidimensional geriatric assessment (MGA) reduced toxicity in G8 ≤ 14 patients.

conclusionFFX is feasible in highly selected elderly patients with PDAC. Severe toxicity remains frequent and proactive supportive care-including MGA in cases of G8 ≤ 14-to avoid early severe toxicity that impact significantly survival.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalPancreatic NeoplasmsAgedAged, 80 and overFemaleFluorouracilHumansIrinotecanLeucovorinMaleOxaliplatinRetrospective StudiesFluorouracilfolfirinoxIrinotecanLeucovorinOxaliplatin

Identifiers

PMID41397201
PMCPMC13086119

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Registered trials

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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.