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Equivalent Efficacy but Different Safety Profiles of Gemcitabine Plus Nab-Paclitaxel and FOLFIRINOX in Metastatic Pancreatic Cancer

Authors :
Caterina Vivaldi
Giulia Bartolini
Giovanni Luca Frassineti
Andrea Casadei-Gardini
Alessandro Cucchetti
Valentina Massa
Ilario Giovanni Rapposelli
Alessandro Passardi
Laura Bernardini
Rapposelli I.G.
Casadei-Gardini A.
Vivaldi C.
Bartolini G.
Bernardini L.
Passardi A.
Frassineti G.L.
Massa V.
Cucchetti A.
Source :
Biomolecules, Vol 11, Iss 780, p 780 (2021), Biomolecules, Volume 11, Issue 6
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

FOLFIRINOX (FFX) and gemcitabine + nab-paclitaxel (GN) are the most common chemotherapy regimens in first-line treatment of metastatic pancreatic cancer (PC). They have not been compared each other in a prospective trial, but only in retrospective studies, which can thus be affected by several biases. In order to overcome these biases, we took advantage of matching-adjusted indirect comparison (MAIC), that allows an indirect comparison by reducing cross-trial differences, and compared data from 268 patients treated with GN in a real-world setting with data from the 171 patients included in the FFX arm of the PRODIGE trial. Survival outcomes did not differ between the two populations. Overall survival was 11.1 months for both treatments (hazard ratio (HR) of FFX 1.10, 95% confidence interval (CI) 0.81–1.49<br />p = 0.527). Progression-free survival was 6.0 months with GN and 6.4 months with FFX (HR of FFX 1.11, 95% CI 0.82–1.50<br />p = 0.520). On the other hand, we observed a difference in the toxicity profiles: grade 3/4 anemia was more frequent with GN, whereas a higher occurrence of grade 3/4 vomiting and diarrhea was reported with FFX. FFX and GN show an equivalent efficacy but different safety profiles in the first-line therapy of metastatic pancreatic cancer. Searching for reliable predictive biomarkers is advised in order to improve therapeutic strategy in metastatic PC.

Details

Language :
English
Volume :
11
Issue :
780
Database :
OpenAIRE
Journal :
Biomolecules
Accession number :
edsair.doi.dedup.....958f88b342d0aa503056c2fa0a503fc1