Comparative outcomes of continuous infusion versus intravenous push followed by infusion 5-fluorouracil in patients with pancreatic and colon cancer: A propensity-matched analysis.

e15735 Background: 5-Fluorouracil (5-FU) is a cornerstone of therapy for gastrointestinal malignancies and is commonly administered as continuous infusion or as intravenous (IV) push followed by infusion. Despite widespread use of bolus-containing regimens, real-world comparative data evaluating clinical outcomes between these administration strategies in pancreatic and colon cancer remain limited. Methods: We conducted a retrospective cohort study using the TriNetX US Collaborative Network, including adults (≥18 years) with pancreatic or colon cancer who received injectable 5-FU between January 2000 and January 2026. Patients were categorized into continuous infusion 5-FU versus IV push followed by infusion 5-FU. Capecitabine exposure was excluded. Outcomes assessed from 1 to 365 days after the index event included all-cause mortality, hospitalization, granulocyte colony-stimulating factor (G-CSF) use, blood transfusion, platelet count < 50×10³/µL, and platelet count < 10×10³/µL. Propensity score matching (1:1) was performed to balance demographics, comorbidities, procedures, concomitant therapies, and genomic variables. Time-to-event outcomes were analyzed using Kaplan–Meier methods with log-rank testing, with Cox proportional hazards models used for effect estimation. Results: After propensity score matching, 8,256 patients were included (4,138 per cohort) with well-balanced baseline characteristics. At 1 year, mortality occurred more frequently in the continuous infusion group compared with the IV push followed by infusion group (8.6% vs 7.5%; risk difference 1.1%, p = 0.068). Kaplan–Meier analysis demonstrated a trend toward improved survival with IV push followed by infusion (log-rank p = 0.053). The hazard ratio did not reach statistical significance (HR 1.16, 95% CI 1.00–1.35, p = 0.074), suggesting a modest and potentially time-dependent difference in survival. No statistically significant differences were observed between groups for hospitalization (log-rank p = 0.349), G-CSF use (log-rank p = 0.303), blood transfusion (log-rank p = 0.527), platelet count < 50×10³/µL (log-rank p = 0.286), or platelet count < 10×10³/µL (log-rank p = 0.525). Conclusions: In this large real-world analysis of patients with pancreatic and colon cancer, IV push followed by infusion 5-FU demonstrated comparable safety outcomes and a trend toward improved survival compared with continuous infusion alone. While differences did not reach statistical significance, Kaplan–Meier analyses suggest potential time-dependent survival differences that warrant further investigation. Prospective studies are needed to clarify the optimal 5-FU administration strategy.

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Journal
Journal of Clinical Oncology
Published
2026-05-28
DOI
https://doi.org/10.1200/jco.2026.44.16_suppl.e15735
Primary Topic
Pancreatic and Hepatic Oncology Research
Type
article
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article

Comparative outcomes of continuous infusion versus intravenous push followed by infusion 5-fluorouracil in patients with pancreatic and colon cancer: A propensity-matched analysis.

Jamil Nazzal, Canan Dirican, Abdulla Massad, Jasneet Randhawa et al.
Journal of Clinical Oncology
Pancreatic and Hepatic Oncology Research
article

Comparative outcomes of continuous infusion versus intravenous push followed by infusion 5-fluorouracil in patients with pancreatic and colon cancer: A propensity-matched analysis.

Jamil Nazzal, Canan Dirican, Abdulla Massad, Jasneet Randhawa, Mohammad Salameh, Salih Akgun, Ahmad Alkhatib, Sanjay Raj Jain, Zaid Zahid, Bugra Zengin
article en

Abstract

e15735 Background: 5-Fluorouracil (5-FU) is a cornerstone of therapy for gastrointestinal malignancies and is commonly administered as continuous infusion or as intravenous (IV) push followed by infusion. Despite widespread use of bolus-containing regimens, real-world comparative data evaluating clinical outcomes between these administration strategies in pancreatic and colon cancer remain limited. Methods: We conducted a retrospective cohort study using the TriNetX US Collaborative Network, including adults (≥18 years) with pancreatic or colon cancer who received injectable 5-FU between January 2000 and January 2026. Patients were categorized into continuous infusion 5-FU versus IV push followed by infusion 5-FU. Capecitabine exposure was excluded. Outcomes assessed from 1 to 365 days after the index event included all-cause mortality, hospitalization, granulocyte colony-stimulating factor (G-CSF) use, blood transfusion, platelet count < 50×10³/µL, and platelet count < 10×10³/µL. Propensity score matching (1:1) was performed to balance demographics, comorbidities, procedures, concomitant therapies, and genomic variables. Time-to-event outcomes were analyzed using Kaplan–Meier methods with log-rank testing, with Cox proportional hazards models used for effect estimation. Results: After propensity score matching, 8,256 patients were included (4,138 per cohort) with well-balanced baseline characteristics. At 1 year, mortality occurred more frequently in the continuous infusion group compared with the IV push followed by infusion group (8.6% vs 7.5%; risk difference 1.1%, p = 0.068). Kaplan–Meier analysis demonstrated a trend toward improved survival with IV push followed by infusion (log-rank p = 0.053). The hazard ratio did not reach statistical significance (HR 1.16, 95% CI 1.00–1.35, p = 0.074), suggesting a modest and potentially time-dependent difference in survival. No statistically significant differences were observed between groups for hospitalization (log-rank p = 0.349), G-CSF use (log-rank p = 0.303), blood transfusion (log-rank p = 0.527), platelet count < 50×10³/µL (log-rank p = 0.286), or platelet count < 10×10³/µL (log-rank p = 0.525). Conclusions: In this large real-world analysis of patients with pancreatic and colon cancer, IV push followed by infusion 5-FU demonstrated comparable safety outcomes and a trend toward improved survival compared with continuous infusion alone. While differences did not reach statistical significance, Kaplan–Meier analyses suggest potential time-dependent survival differences that warrant further investigation. Prospective studies are needed to clarify the optimal 5-FU administration strategy.

Journal of Clinical OncologyVol. 44(16_suppl)
Medical University of South Carolina (US), MedStar Harbor Hospital (US), St. Mary's Hospital (US), Hamilton Medical Center (US), Hackensack Meridian Health (US), The University of Texas Medical Branch at Galveston (US), MedStar Health (US)
Good health and well-being
Openalex Percentile: Top 7%
Pancreatic and Hepatic Oncology Research
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