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Multicenter Retrospective Analysis of Original versus Modified FOLFIRINOX in Metastatic Pancreatic Cancer: Results of the NAPOLEON Study.

Authors :
Nakazawa J
Tsuruta N
Shimokawa M
Kawahira M
Arima S
Ido A
Koga F
Ueda Y
Komori A
Otsu S
Fukahori M
Makiyama A
Taguchi H
Honda T
Shibuki T
Nio K
Ide Y
Ureshino N
Mizuta T
Otsuka T
Shirakawa T
Mitsugi K
Source :
Oncology [Oncology] 2023; Vol. 101 (1), pp. 22-31. Date of Electronic Publication: 2022 Oct 04.
Publication Year :
2023

Abstract

Introduction: Original FOLFIRINOX (oFFX) is more toxic than other regimens for patients with metastatic pancreatic cancer (mPC); therefore, a modified FFX (mFFX) regimen with a reduced dosage has been used in Japanese clinical practice. However, very few studies have compared these two regimens.<br />Methods: This study was conducted as part of a multicenter retrospective study of 318 patients with mPC across 14 centers in Japan (NAPOLEON study). To control for potential bias and confounders, we conducted a propensity score-adjusted analysis of patient characteristics and clinical outcomes.<br />Results: oFFX and mFFX were administered to 48 and 54 patients. More patients with younger age and poorer performance status were included in the oFFX group. The overall survival (OS; median, 11.6 vs. 11.3 months; hazard ratio [HR], 0.91; 95% confidence interval [CI], 0.60-1.40; p = 0.67), progression-free survival (PFS) (median, 6.3 vs. 5.7 months; HR, 0.85; 95% CI, 0.56-1.28; p = 0.44), and overall response rate (29 vs. 26%, p = 0.71) were not significantly different for the oFFX and mFFX groups. Thrombopenia and liver dysfunction were significantly more frequent with oFFX than with mFFX. The median received dose intensity of CPT-11 was higher with oFFX than with mFFX (299 vs. 270 mg/m2/week, p < 0.01). The propensity score-adjusted analysis revealed no statistically significant differences in OS and PFS between the two groups.<br />Conclusion: In our data, there was no significant difference in efficacy between mFFX and oFFX, and mFFX has fewer adverse events.<br /> (© 2022 S. Karger AG, Basel.)

Details

Language :
English
ISSN :
1423-0232
Volume :
101
Issue :
1
Database :
MEDLINE
Journal :
Oncology
Publication Type :
Academic Journal
Accession number :
36195058
Full Text :
https://doi.org/10.1159/000527176