Gemcitabine/nab-Paclitaxel versus FOLFIRINOX for palliative first-line treatment of advanced pancreatic cancer: A propensity score analysis.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
07 2021
Historique:
received: 17 01 2021
revised: 13 03 2021
accepted: 24 03 2021
pubmed: 6 5 2021
medline: 9 11 2021
entrez: 5 5 2021
Statut: ppublish

Résumé

Gemcitabine/nab-paclitaxel (GN) and FOLFIRINOX are standard first-line treatment options for advanced pancreatic ductal adenocarcinoma (aPDAC), but currently no prospective randomised head-to-head comparison between these treatments has yet been performed. We conducted a comparative propensity score (PS) analysis of overall (OS) and progression-free survival (PFS) in a tri-centre cohort of patients with aPDAC undergoing palliative first-line treatment with either GN or FOLFIRINOX. In unadjusted analysis, OS and PFS were highly similar between patients treated with GN (n = 297) and FOLFIRINOX (n = 158). In detail, median, 1- and 2-year OS estimates were 10.1 months, 42% and 18% in the GN group, as compared to 11.2 months, 45% and 12% in the FOLFIRINOX group, respectively (log-rank p = 0.783). Accordingly, median (4.6 versus 4.8 months), 6-month (40% versus 43%) and 1-year (9% versus 9%) PFS estimates did not significantly differ (log-rank p = 0.717). However, patients treated with FOLFIRINOX were significantly younger, had fewer comorbidities, and a better Eastern Cooperative Oncology Group performance status. These imbalances were accounted for by weighting the data with the PS. In PS analysis of survival outcomes, OS and PFS remained comparable between the two treatment groups. In detail, PS-weighted median, 1- and 2-year OS estimates were 10.1 months, 42% and 18% in the GN group, as compared to 10.1 months, 40% and 13% in the FOLFIRINOX group (PS-weighted log-rank p = 0.449). PS-weighted PFS estimates again did not differ (PS-weighted log-rank p = 0.329). This real-world comparative effectiveness study indicates that FOLFIRINOX and GN have similar effectiveness in the palliative first-line treatment of aPDAC.

Sections du résumé

BACKGROUND
Gemcitabine/nab-paclitaxel (GN) and FOLFIRINOX are standard first-line treatment options for advanced pancreatic ductal adenocarcinoma (aPDAC), but currently no prospective randomised head-to-head comparison between these treatments has yet been performed.
METHODS
We conducted a comparative propensity score (PS) analysis of overall (OS) and progression-free survival (PFS) in a tri-centre cohort of patients with aPDAC undergoing palliative first-line treatment with either GN or FOLFIRINOX.
RESULTS
In unadjusted analysis, OS and PFS were highly similar between patients treated with GN (n = 297) and FOLFIRINOX (n = 158). In detail, median, 1- and 2-year OS estimates were 10.1 months, 42% and 18% in the GN group, as compared to 11.2 months, 45% and 12% in the FOLFIRINOX group, respectively (log-rank p = 0.783). Accordingly, median (4.6 versus 4.8 months), 6-month (40% versus 43%) and 1-year (9% versus 9%) PFS estimates did not significantly differ (log-rank p = 0.717). However, patients treated with FOLFIRINOX were significantly younger, had fewer comorbidities, and a better Eastern Cooperative Oncology Group performance status. These imbalances were accounted for by weighting the data with the PS. In PS analysis of survival outcomes, OS and PFS remained comparable between the two treatment groups. In detail, PS-weighted median, 1- and 2-year OS estimates were 10.1 months, 42% and 18% in the GN group, as compared to 10.1 months, 40% and 13% in the FOLFIRINOX group (PS-weighted log-rank p = 0.449). PS-weighted PFS estimates again did not differ (PS-weighted log-rank p = 0.329).
CONCLUSION
This real-world comparative effectiveness study indicates that FOLFIRINOX and GN have similar effectiveness in the palliative first-line treatment of aPDAC.

Identifiants

pubmed: 33951545
pii: S0959-8049(21)00207-0
doi: 10.1016/j.ejca.2021.03.040
pii:
doi:

Substances chimiques

130-nm albumin-bound paclitaxel 0
Albumins 0
Antimetabolites, Antineoplastic 0
folfirinox 0
Oxaliplatin 04ZR38536J
Deoxycytidine 0W860991D6
Irinotecan 7673326042
Paclitaxel P88XT4IS4D
Leucovorin Q573I9DVLP
Fluorouracil U3P01618RT
Gemcitabine 0

Types de publication

Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

3-13

Informations de copyright

Copyright © 2021 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement RG, AD and AG have received honoraria from Celgene and have been members of the consulting or advisory role for Celgene. The other authors declare no conflict of interest.

Auteurs

Jakob M Riedl (JM)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Florian Posch (F)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Lena Horvath (L)

Department of Internal Medicine V: Hematology and Oncology, Medical University of Innsbruck, Innsbruck, Austria.

Antonia Gantschnigg (A)

Department of Surgery, Paracelsus Medical University, Salzburg, Austria.

Felix Renneberg (F)

IIIrd Medical Department of Hematology, Medical Oncology, Hemostaseology, Rheumatology and Infectious Disease, Salzburg Cancer Research Institute, Paracelsus Medical University, Salzburg, Austria.

Esther Schwarzenbacher (E)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Florian Moik (F)

Clinical Division of Hematology and Hemostaseology, Department of Medicine I, Comprehensive Cancer Center Vienna, Medical University of Vienna, Vienna, Austria.

Dominik A Barth (DA)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Christopher H Rossmann (CH)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Michael Stotz (M)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Renate Schaberl-Moser (R)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Martin Pichler (M)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Herbert Stöger (H)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Richard Greil (R)

IIIrd Medical Department of Hematology, Medical Oncology, Hemostaseology, Rheumatology and Infectious Disease, Salzburg Cancer Research Institute, Paracelsus Medical University, Salzburg, Austria.

Angela Djanani (A)

Department of Internal Medicine I: Gastroenterology and Hepatology, Medical University of Innsbruck, Innsbruck, Austria.

Konstantin Schlick (K)

IIIrd Medical Department of Hematology, Medical Oncology, Hemostaseology, Rheumatology and Infectious Disease, Salzburg Cancer Research Institute, Paracelsus Medical University, Salzburg, Austria.

Armin Gerger (A)

Division of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria. Electronic address: armin.gerger@medunigraz.at.

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Classifications MeSH