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FOLFIRINOX relative dose intensity and disease control in advanced pancreatic adenocarcinoma

Authors :
Antonin Vary
Loïc Lebellec
Frédéric Di Fiore
Nicolas Penel
Claire Cheymol
Emilia Rad
Farid El Hajbi
Astrid Lièvre
Julien Edeline
André Michel Bimbai
Marie-Cécile Le Deley
Anthony Turpin
Source :
Therapeutic Advances in Medical Oncology, Vol 13 (2021)
Publication Year :
2021
Publisher :
SAGE Publishing, 2021.

Abstract

Background: Most patients with advanced pancreatic adenocarcinoma (PA) treated with FOLFIRINOX experience adverse events requiring dose reduction. We aimed to assess the association between relative dose intensity (RDI) and disease control in a European setting. Methods: We retrospectively included patients with advanced PA treated with three or more cycles of FOLFIRINOX between 2011 and 2018 in six French centers. We computed the cumulative single-agent RDI (csRDI) before the first reassessment for each FOLFIRINOX agent (oxaliplatin, irinotecan, 5FU bolus, and 5FU intravenous infusion) and the cumulative multi-drug RDI (cmRDI) of their combination. The association between RDI and disease control or objective response at first reassessment was evaluated using multivariable logistic regression models controlling for performance status, liver metastases, and center. Results: We included 243 patients. Median csRDIs were 81%, 79%, 75%, and 85% for oxaliplatin, irinotecan, 5FU bolus, and 5FU intravenous infusion, respectively. Median cmRDI was 80%. None of the RDIs was significantly associated with disease control or objective response. Including RDI in a clinical model did not improve its ability to predict disease control; the area under the curve was 0.79 (95% CI: 0.73–0.85) with RDI versus 0.78 (95% CI: 0.72–0.85) without. Similar results were observed for the objective response. Conclusion: Pragmatic dose adjustments of FOLFIRINOX should be made by oncologists without considering a loss of effect.

Details

Language :
English
ISSN :
17588359
Volume :
13
Database :
Directory of Open Access Journals
Journal :
Therapeutic Advances in Medical Oncology
Publication Type :
Academic Journal
Accession number :
edsdoj.503d95fdec94c7eb3de50d752b7ba3e
Document Type :
article
Full Text :
https://doi.org/10.1177/17588359211029825