Evidence map›Paper›PMID 41769085›Full record

ArticleClinical Medicine Insights. Oncology2026

First-Line Modified FOLFIRINOX in Metastatic Pancreatic Cancer: Real-World Outcomes and Prognostic Factors From a Vietnamese Cohort.

Huy Van Nguyen, Phuong Thi Dinh, Thang Tran, Cuc Thi Hoang

Abstract read
In one paragraph

Article in Clinical Medicine Insights. Oncology, 2026. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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

4 authors.

Huy Van NguyenDepartment of Medical Oncology, National Cancer Hospital, Hanoi, Vietnam.ORCID https://orcid.org/0009-0006-4784-3795
Phuong Thi DinhDepartment of Medical Oncology, Nghe An Oncology Hospital, Nghe An, Vietnam.
Thang TranDepartment of Medical Oncology, National Cancer Hospital, Hanoi, Vietnam.
Cuc Thi HoangDepartment of Medical Oncology, National Cancer Hospital, Hanoi, Vietnam.ORCID https://orcid.org/0009-0009-3010-1957

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Metastatic pancreatic cancer is an aggressive malignancy with limited survival despite intensive chemotherapy. While modified FOLFIRINOX (mFOLFIRINOX) has illustrated efficacy, its real-world data are limited in low-resource healthcare systems. This study evaluated efficacy and toxicity and identified prognostic factors of mFOLFIRINOX as a first-line therapy for Vietnamese patients with metastatic pancreatic cancer. Methods: We conducted a retrospective cohort study of 36 patients receiving mFOLFIRINOX as first-line therapy. All patients received peg-filgrastim as the primary prophylaxis. An application of flexible treatment approach-interruption was permitted between cycles under physician guidance. Progression-free survival (PFS), overall survival (OS), tumor response, and adverse events were assessed. Prognostic factors were analyzed using log-rank tests and Cox regression models. Results: The median follow-up was 15.6 months (95% confidence interval [CI] 3.8-27.3). The overall response rate (ORR) was 30.6 %, and the disease control rate (DCR) was 66.6%. The median progression-free survival was 6.7 (95% CI 5.4-8) months, and the median overall survival was 12.5 (95% CI 9.5-15.4) months. Grade 3 or 4 toxicities were mainly hematologic, including neutropenia in 33.4%, and anemia in 5.6% of patients. No cases of febrile neutropenia were observed. Univariate analyses identified performance status (PS) and age under 60 years as associated with improved outcomes. In multivariate Cox regression, PS remained an independent prognostic factor for overall survival. Conclusion: mFOLFIRINOX regimen demonstrated efficacy and manageable toxicity in Vietnamese patients with metastatic pancreatic cancer. An individualized approach involving treatment interruptions was observed in patients with relatively favorable outcomes. These findings support the feasibility of the regimen in real-world settings.

Indexed as

flexible treatment approachMetastatic pancreatic cancermodified FOLFIRINOXreal-world datatreatment interruption

Identifiers

PMID41769085
PMCPMC12936372

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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.