Second-line and third-line therapy with nanoliposomal irinotecan (nal-IRI) in pancreatic cancer: a single-center experience and review of literature.

FOLFIRINOX irinotecan resistance nal-irinotecan palliative chemotherapy pancreatic cancer

Journal

Journal of gastrointestinal oncology
ISSN: 2078-6891
Titre abrégé: J Gastrointest Oncol
Pays: China
ID NLM: 101557751

Informations de publication

Date de publication:
28 Feb 2023
Historique:
received: 01 07 2022
accepted: 07 11 2022
entrez: 14 3 2023
pubmed: 15 3 2023
medline: 15 3 2023
Statut: ppublish

Résumé

Prognosis of patients with pancreatic cancer is still extremely poor. First-line palliative therapies with FOLFIRINOX or gemcitabine/nab-paclitaxel have been established in the last decade. In the second-line, 5-FU/LV in combination with nanoliposomal irinotecan (nal-IRI) after gemcitabine has been shown to be effective. However, the use of nal-IRI as third-line therapy after FOLFIRINOX and gemcitabine-based chemotherapies is still controversial. In this study, we report about the use of 5-FU/LV + nal-IRI in a daily practice and analyze whether nal-IRI is an option as third-line therapy after FOLFIRINOX and gemcitabine/nab-paclitaxel. This is a single center retrospective analysis of patients with irresectable pancreatic cancer who were treated with 5-FU/LV and nal-IRI from 2017 to 2021 as second- or third-line palliative treatment. Overall survival (OS), progression-free survival (PFS) and toxicity were analyzed, and multivariate analysis was used to identify independent prognostic factors. Twenty-nine patients receiving 5-FU/LV and nal-IRI were included in the analysis. The majority of patients (n=19) received 5-FU/nal-IRI as third-line therapy after pre-exposition to FOLFIRINOX and gemcitabine/nab-paclitaxel. Median OS and PFS were 9.33 months (95% CI: 3.37, 15.30) and 2.90 months (95% CI: 1.64, 4.16), respectively. Furthermore, patients receiving nal-IRI + 5-FU/LV as third-line treatment also showed some benefits, with no OS difference compared to second-line patients (9.33 In our study, the use of 5-FU/nal-IRI in unselected patients with advanced pancreatic cancer showed similar OS, PFS and tolerance as randomized prospective phase II/III trials. Interestingly, the use of 5-FU/nal-IRI seemed to be beneficial in third-line therapy, despite a pre-exposure to non-liposomal irinotecan.

Sections du résumé

Background UNASSIGNED
Prognosis of patients with pancreatic cancer is still extremely poor. First-line palliative therapies with FOLFIRINOX or gemcitabine/nab-paclitaxel have been established in the last decade. In the second-line, 5-FU/LV in combination with nanoliposomal irinotecan (nal-IRI) after gemcitabine has been shown to be effective. However, the use of nal-IRI as third-line therapy after FOLFIRINOX and gemcitabine-based chemotherapies is still controversial. In this study, we report about the use of 5-FU/LV + nal-IRI in a daily practice and analyze whether nal-IRI is an option as third-line therapy after FOLFIRINOX and gemcitabine/nab-paclitaxel.
Methods UNASSIGNED
This is a single center retrospective analysis of patients with irresectable pancreatic cancer who were treated with 5-FU/LV and nal-IRI from 2017 to 2021 as second- or third-line palliative treatment. Overall survival (OS), progression-free survival (PFS) and toxicity were analyzed, and multivariate analysis was used to identify independent prognostic factors.
Results UNASSIGNED
Twenty-nine patients receiving 5-FU/LV and nal-IRI were included in the analysis. The majority of patients (n=19) received 5-FU/nal-IRI as third-line therapy after pre-exposition to FOLFIRINOX and gemcitabine/nab-paclitaxel. Median OS and PFS were 9.33 months (95% CI: 3.37, 15.30) and 2.90 months (95% CI: 1.64, 4.16), respectively. Furthermore, patients receiving nal-IRI + 5-FU/LV as third-line treatment also showed some benefits, with no OS difference compared to second-line patients (9.33
Conclusions UNASSIGNED
In our study, the use of 5-FU/nal-IRI in unselected patients with advanced pancreatic cancer showed similar OS, PFS and tolerance as randomized prospective phase II/III trials. Interestingly, the use of 5-FU/nal-IRI seemed to be beneficial in third-line therapy, despite a pre-exposure to non-liposomal irinotecan.

Identifiants

pubmed: 36915455
doi: 10.21037/jgo-22-632
pii: jgo-14-01-352
pmc: PMC10007927
doi:

Types de publication

Journal Article

Langues

eng

Pagination

352-365

Informations de copyright

2023 Journal of Gastrointestinal Oncology. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://jgo.amegroups.com/article/view/10.21037/jgo-22-632/coif). MG has contributed to advisory boards for Roche, Eisai, BMS, MSD and AZ. However, these activities have no potential conflicts of interest with the manuscript. This work was supported by the following grants awarded to MG: GO 1874/1-2 grant from “Deutsche Forschungsgemeinschaft” (DFG), BONFOR from the University of Bonn, grant number 109255 from “Deutsche Krebshilfe” (German Cancer Aid) and a grant from the Reuthersche endowment fund of the University of Bonn. TRG serves as an unpaid editorial board of the German Pancreas Club and was elected congress president for 2024 on the annual conference in 2022, not connected to the submitted work. The other authors have no conflicts of interest to declare.

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Auteurs

Christian Möhring (C)

Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.

Freddy José Frontado Graffe (FJ)

Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.

Alexandra Bartels (A)

Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.

Farsaneh Sadeghlar (F)

Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.

Taotao Zhou (T)

Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.

Robert Mahn (R)

Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.

Milka Marinova (M)

Department of Nuclear Medicine, University Hospital Bonn, Bonn, Germany.

Georg Feldmann (G)

Department of Internal Medicine III, University Hospital Bonn, Bonn, Germany.

Peter Brossart (P)

Department of Internal Medicine III, University Hospital Bonn, Bonn, Germany.

Tim R Glowka (TR)

Department of Visceral Surgery, University Hospital Bonn, Bonn, Germany.

Jörg C Kalff (JC)

Department of Visceral Surgery, University Hospital Bonn, Bonn, Germany.

Christian P Strassburg (CP)

Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.

Maria A Gonzalez-Carmona (MA)

Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.

Classifications MeSH