Open Access
Open access
Cancer Medicine, volume 12, issue 13, pages 14337-14345

The role of nanoliposomal irinotecan plus fluorouracil/leucovorin in the continuum of care of patients with metastatic pancreatic ductal adenocarcinoma

Letizia Procaccio 1, 2
Valeria Merz 3
Morena Fasano 4
Vanja Vaccaro 5
Elisa Giommoni 6
Andrea Pretta 7
Silvia Noventa 8
Maria Antonietta Satolli 9
Guido Giordano 10
Clizia Zichi 11
Carmine Pinto 12
Camilla Zecchetto 3
Giulia Barsotti 1, 2
Ferdinando De Vita 4
Michele Milella 5
Antonuzzo Lorenzo 6, 13
Mario Scartozzi 7
Alberto Zaniboni 8
Rosella Spadi 14
Simona Casalino 3
Francesca Bergamo 1
Chiara De Toni 1
Davide Melisi 3, 15
Sara Lonardi 16
Show full list: 24 authors
8
 
Medical Oncology Unit Casa di Cura Poliambulanza Brescia Italy
14
 
Medical Oncology 1 Azienda Ospedaliero‐Universitaria Città della Salute e della Scienza Turin Italy
Publication typeJournal Article
Publication date2023-06-06
Journal: Cancer Medicine
scimago Q1
SJR1.174
CiteScore5.5
Impact factor2.9
ISSN20457634
Cancer Research
Oncology
Radiology, Nuclear Medicine and imaging
Abstract
Background

The NAPOLI‐I trial showed better outcome of nanoliposomal irinotecan (nal‐IRI) plus 5‐fluorouracil/leucovorin (5‐FU/LV) compared to 5‐FU/LV in patients with advanced pancreatic ductal adenocarcinoma cancer (advPDAC) progressed to gemcitabine‐based therapy. This study aims to explore the real‐world efficacy and safety of 5‐FU/LV‐nal‐IRI.

Methods

This is a retrospective multicenter analysis including advPDAC patients receiving 5‐FU/LV‐nal‐IRI after failure of gemcitabine‐based therapy. Survival analyses were performed using Kaplan–Meier method, univariate and multivariate analyses by Cox regression.

Results

A total of 296 patients (median age 64.4 years, ECOG PS ≥1 in 56% of cases) were treated at 11 Italian institutions between 2016 and 2018. 34% of them underwent primary tumor resection, and 79% received gemcitabine‐nabpaclitaxel as first line. 5‐FU/LV‐nal‐IRI was administered as second‐line in 73% of cases.

Objective response and disease control rate were 12% and 41%, respectively. Treatment was well tolerated with dose reductions in 50% of patients but no one permanent discontinuation; the commonest grade ≥3 toxicities were neutropenia (14%) and diarrhea (12%). Median PFS and OS from 5‐FU/LV‐nal‐IRI initiation was 3.2 and 7.1 months, respectively.

Conclusions

These real‐world data confirm the 5‐FU/LV‐nal‐IRI efficacy and safety in advPDAC patients progressed to gemcitabine‐based therapy, with outcomes comparable to NAPOLI‐1, even in a less‐selected population and with more modern therapeutic algorithm.

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