FOLFIRINOX vs. gemcitabine/nab-paclitaxel for metastatic pancreatic cancer: A real-world study

BACKGROUND: FOLFIRINOX and gemcitabine/nab-paclitaxel are widely used first-line regimens in metastatic pancreatic cancer (mPC); however, direct real-world comparisons and clear criteria for selecting between the two remain limited. METHODS: In this retrospective cohort study, we used a multicenter real-world data registry to compare outcomes between patients with mPC treated with FOLFIRINOX and gemcitabine/nab-paclitaxel and explore associations between genomic alterations and survival outcomes. The cohort included patients with mPC treated with FOLFIRINOX (n = 272) or gemcitabine/nab-paclitaxel (n = 280) between 2010 and 2022 at tertiary referral cancer centers. The primary outcomes were overall and progression-free survival. Available next-generation sequencing results were used to explore potential prognostic biomarkers. FINDINGS: The FOLFIRINOX group was significantly younger than the gemcitabine/nab-paclitaxel group. Before propensity score matching, the FOLFIRINOX group showed significantly longer median overall and progression-free survival. Afterward, survival outcomes no longer significantly differed. Next-generation sequencing panel data were available for 57 and 29 patients in the FOLFIRINOX and gemcitabine/nab-paclitaxel groups, respectively. In the gemcitabine/nab-paclitaxel group, ARID1A and RNF43 mutations were correlated with shorter progression-free survival. Genomic alterations in the TGF-β pathway were associated with longer overall survival with gemcitabine/nab-paclitaxel. INTERPRETATION: No statistically significant differences in OS or PFS were observed between FOLFIRINOX and gemcitabine/nab-paclitaxel after propensity score matching. The exploratory genomic associations require validation in larger prospective cohorts before their potential role in treatment selection can be established. FUNDING: This work was supported by grants from the National Research Foundation of Korea (RS-2024-00,335,625, RS-2024-00,342,475, and NRF-2021R1A2C1008898), Korea Evaluation Institute of Industrial Technology (20,023,781), and Korea Health Technology R&D Project through the Korea Health Industry Development Institute (HI22C047400).

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Publication Details

Journal
Translational Oncology
Published
2026-10-26
DOI
https://doi.org/10.1016/j.tranon.2026.103085
Primary Topic
Pancreatic and Hepatic Oncology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

FOLFIRINOX vs. gemcitabine/nab-paclitaxel for metastatic pancreatic cancer: A real-world study

Galam Leem, Jung Hyun Jo, Jeong Youp Park, Si Young Song et al.
Translational Oncology
Pancreatic and Hepatic Oncology Research
article

FOLFIRINOX vs. gemcitabine/nab-paclitaxel for metastatic pancreatic cancer: A real-world study

Galam Leem, Jung Hyun Jo, Jeong Youp Park, Si Young Song, Jee Hoon Kim, M. Chung, See Young Lee, Jae Hee Cho, Sung Ill Jang, Hee Seung Lee, Seung Woo Park, Seungmin Bang
article en

Abstract

BACKGROUND: FOLFIRINOX and gemcitabine/nab-paclitaxel are widely used first-line regimens in metastatic pancreatic cancer (mPC); however, direct real-world comparisons and clear criteria for selecting between the two remain limited. METHODS: In this retrospective cohort study, we used a multicenter real-world data registry to compare outcomes between patients with mPC treated with FOLFIRINOX and gemcitabine/nab-paclitaxel and explore associations between genomic alterations and survival outcomes. The cohort included patients with mPC treated with FOLFIRINOX (n = 272) or gemcitabine/nab-paclitaxel (n = 280) between 2010 and 2022 at tertiary referral cancer centers. The primary outcomes were overall and progression-free survival. Available next-generation sequencing results were used to explore potential prognostic biomarkers. FINDINGS: The FOLFIRINOX group was significantly younger than the gemcitabine/nab-paclitaxel group. Before propensity score matching, the FOLFIRINOX group showed significantly longer median overall and progression-free survival. Afterward, survival outcomes no longer significantly differed. Next-generation sequencing panel data were available for 57 and 29 patients in the FOLFIRINOX and gemcitabine/nab-paclitaxel groups, respectively. In the gemcitabine/nab-paclitaxel group, ARID1A and RNF43 mutations were correlated with shorter progression-free survival. Genomic alterations in the TGF-β pathway were associated with longer overall survival with gemcitabine/nab-paclitaxel. INTERPRETATION: No statistically significant differences in OS or PFS were observed between FOLFIRINOX and gemcitabine/nab-paclitaxel after propensity score matching. The exploratory genomic associations require validation in larger prospective cohorts before their potential role in treatment selection can be established. FUNDING: This work was supported by grants from the National Research Foundation of Korea (RS-2024-00,335,625, RS-2024-00,342,475, and NRF-2021R1A2C1008898), Korea Evaluation Institute of Industrial Technology (20,023,781), and Korea Health Technology R&D Project through the Korea Health Industry Development Institute (HI22C047400).

Translational OncologyVol. 74
Yonsei University (KR), Kangbuk Samsung Hospital (KR), Gangnam Severance Hospital (KR), Sungkyunkwan University (KR)
Ministry of Trade, Industry and Energy, Ministry of Health and Welfare, Korea Health Industry Development Institute, National Research Foundation of Korea, Ministry of Science and ICT, South Korea, Korea Evaluation Institute of Industrial Technology
Openalex Percentile: Top 16%
Pancreatic and Hepatic Oncology Research
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