Evidence map›Paper›PMID 40936050›Full record

ArticleJournal of gastrointestinal cancer2025

Clinical Outcome and Safety of Triweekly Modified FOLFIRINOX Therapy in Patients with Advanced Pancreatic Cancer.

Kana Hosokawa, Kenji Ikezawa, Yugo Kai, Ryoji Takada, Takumi Kinomoto, Takanori Masumoto, Masaki Kawabata, Hiroki Kishimoto, Kazuhiro Kozumi, Makiko Urabe and 3 more

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Article in Journal of gastrointestinal cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Kana HosokawaDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Kenji IkezawaDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan. ikezawa-ke@oici.jp.
Yugo KaiDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Ryoji TakadaDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Takumi KinomotoDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Takanori MasumotoDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Masaki KawabataDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Hiroki KishimotoDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Kazuhiro KozumiDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Makiko UrabeDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Kaori MukaiDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Tasuku NakaboriDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Kazuyoshi OhkawaDepartment of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeModified FOLFIRINOX (mFFX) therapy is widely used as first- or second-line treatment for advanced pancreatic cancer. However, adverse effects (AEs), such as cytopenia, often prevent the intended biweekly administration of mFFX therapy. Extending the dosing interval may decrease AEs and allow safer and longer mFFX therapy continuation. Therefore, this study evaluated the efficacy and safety of triweekly mFFX therapy at our institution.

methodsWe retrospectively reviewed 17 patients with unresectable pancreatic ductal adenocarcinoma who received mFFX therapy for more than 3 months and switched to a triweekly administration schedule within 2 months of initiating therapy at our institution between April 2017 and December 2023.

resultsPatient median age was 58 years (range: 36-75, 52.9% male). Eleven patients received mFFX therapy as the first-line treatment, while the other four patients received it as the second-line treatment. The median number of mFFX cycles was nine (range: 5-56). The median overall survival (OS) and progression-free survival (PFS) for all patients were 14.2 (95% confidence interval [CI], 10.5-26.3) and 6.7 (95% CI, 3.9-9.5) months, respectively. Regarding AEs, because patients with severe hematologic toxicity in the early phase were switched to triweekly treatment, the proportions of grade ≥ 3 leukopenia and neutropenia were high. In contrast, for grade ≥ 3 non-hematologic toxicity, diarrhea and anorexia were observed in only 1 of 17 patients.

conclusionTriweekly mFFX therapy for unresectable pancreatic cancer may be a feasible treatment option, with relatively low toxicity and valid efficacy.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalPancreatic NeoplasmsAdultAgedDrug Administration ScheduleFemaleFluorouracilHumansIrinotecanLeucovorinMaleMiddle AgedOxaliplatinRetrospective StudiesTreatment OutcomeFluorouracilfolfirinoxIrinotecanLeucovorinOxaliplatinChemotherapyExtended dosing intervalsOverall survivalPancreatic cancerTime toxicityToxicity of treatment

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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.