Gemcitabine/Nab-Paclitaxel versus FOLFIRINOX in Locally Advanced Pancreatic Cancer: A European Multicenter Study

Background: Gemcitabine/nab-paclitaxel (GN) and FOLFIRINOX (FFX) are two standard first-line therapies for metastatic pancreatic cancer (PC) but have rarely been compared, especially in patients with locally advanced PC (LAPC). Methods: This is a retrospective European multicenter study including pa...

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Main Authors: Nicolas Williet, Angelica Petrillo, Gaël Roth, Michele Ghidini, Mila Petrova, Julien Forestier, Anthony Lopez, Audrey Thoor, Lucie Weislinger, Ferdinando De Vita, Julien Taieb, Jean Marc Phelip
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Cancers
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Online Access:https://www.mdpi.com/2072-6694/13/11/2797
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author Nicolas Williet
Angelica Petrillo
Gaël Roth
Michele Ghidini
Mila Petrova
Julien Forestier
Anthony Lopez
Audrey Thoor
Lucie Weislinger
Ferdinando De Vita
Julien Taieb
Jean Marc Phelip
author_facet Nicolas Williet
Angelica Petrillo
Gaël Roth
Michele Ghidini
Mila Petrova
Julien Forestier
Anthony Lopez
Audrey Thoor
Lucie Weislinger
Ferdinando De Vita
Julien Taieb
Jean Marc Phelip
author_sort Nicolas Williet
collection DOAJ
description Background: Gemcitabine/nab-paclitaxel (GN) and FOLFIRINOX (FFX) are two standard first-line therapies for metastatic pancreatic cancer (PC) but have rarely been compared, especially in patients with locally advanced PC (LAPC). Methods: This is a retrospective European multicenter study including patients with LAPC treated with either GN or FFX as the first-line therapy between 2010 and 2019. Coprimary objectives were progression-free survival (PFS) and overall survival (OS), both estimated using the Kaplan–Meier method. Results: A total of 147 patients (GN: <i>n</i> = 60; FFX: <i>n</i> = 87) were included. Tumor resection rates were similar between the two groups (16.7% vs. 16.1%; <i>p</i> = 1), with similar R0 resection rates (88.9%). Median PFS rates were not statistically different: 9 months (95% CI: 8–13.5) vs. 12.1 months (95% CI: 10.1–14.6; <i>p</i> = 0.8), respectively. Median OS rates were 15.7 months (95% CI: 12.6–20.2) and 16.7 months (95% CI: 14.8–20.4; <i>p</i> = 0.7), respectively. Abdominal pain at the baseline (HR = 2.03, <i>p</i> = 0.03), tumors located in the tail of the pancreas (HR = 4.35, <i>p</i> = 0.01), CA19-9 > 200 UI/L (HR = 2.03, <i>p</i> = 0.004) and tumor resection (HR = 0.37, <i>p</i> = 0.007) were independent prognostic factors for PFS, similarly to OS. CA19-9 ≤ 200 UI/L (OR = 2.6, <i>p</i> = 0.047) was predictive of the tumor response. Consolidation chemoradiotherapy, more often used in the FFX group (11.7% vs. 50.6%; <i>p</i> < 0.001), was not predictive. Conclusion: This retrospective study did not show any difference between GN and FFX as the first-line treatment in patients with LAPC.
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spelling doaj.art-4dcb159d60094391b06f479e0cbed9b92023-11-21T22:47:00ZengMDPI AGCancers2072-66942021-06-011311279710.3390/cancers13112797Gemcitabine/Nab-Paclitaxel versus FOLFIRINOX in Locally Advanced Pancreatic Cancer: A European Multicenter StudyNicolas Williet0Angelica Petrillo1Gaël Roth2Michele Ghidini3Mila Petrova4Julien Forestier5Anthony Lopez6Audrey Thoor7Lucie Weislinger8Ferdinando De Vita9Julien Taieb10Jean Marc Phelip11Department of Hepatogastroenterology, University Hospital of Saint-Etienne, 42000 Saint-Etienne, FranceDepartment of Precision Medecine, University of Study of Campania «L. Vanvitelli», 81100 Naples, ItalyHepato-Gastroenterology Department, University Hospital of Grenoble, 38043 Grenoble, FranceDepartment of Medical Oncology, Cancer Center, Hospital of Cremona, 26100 Cremona, ItalyDepartment of Medical Oncology, MHAT Nadezhda, 1220 Sofia, BulgariaDepartment of Medical Oncology, Hôpital Edouard Herriot, 69622 Lyon, FranceHepato-Gastroenterology Department, University Hospital of Nancy, 54500 Vandoeuvre-lès-Nancy, FranceHepato-Gastroenterology Department, University Hospital of Grenoble, 38043 Grenoble, FranceHepato-Gastroenterology Department, University Hospital of Nancy, 54500 Vandoeuvre-lès-Nancy, FranceDepartment of Precision Medecine, University of Study of Campania «L. Vanvitelli», 81100 Naples, ItalyDepartment of Gastroenterology and Gastro-Intestinal Oncology, Hôpital Européen Georges-Pompidou, APHP, Paris Descartes University, Sorbonne Paris Cité, 75004 Paris, FranceDepartment of Hepatogastroenterology, University Hospital of Saint-Etienne, 42000 Saint-Etienne, FranceBackground: Gemcitabine/nab-paclitaxel (GN) and FOLFIRINOX (FFX) are two standard first-line therapies for metastatic pancreatic cancer (PC) but have rarely been compared, especially in patients with locally advanced PC (LAPC). Methods: This is a retrospective European multicenter study including patients with LAPC treated with either GN or FFX as the first-line therapy between 2010 and 2019. Coprimary objectives were progression-free survival (PFS) and overall survival (OS), both estimated using the Kaplan–Meier method. Results: A total of 147 patients (GN: <i>n</i> = 60; FFX: <i>n</i> = 87) were included. Tumor resection rates were similar between the two groups (16.7% vs. 16.1%; <i>p</i> = 1), with similar R0 resection rates (88.9%). Median PFS rates were not statistically different: 9 months (95% CI: 8–13.5) vs. 12.1 months (95% CI: 10.1–14.6; <i>p</i> = 0.8), respectively. Median OS rates were 15.7 months (95% CI: 12.6–20.2) and 16.7 months (95% CI: 14.8–20.4; <i>p</i> = 0.7), respectively. Abdominal pain at the baseline (HR = 2.03, <i>p</i> = 0.03), tumors located in the tail of the pancreas (HR = 4.35, <i>p</i> = 0.01), CA19-9 > 200 UI/L (HR = 2.03, <i>p</i> = 0.004) and tumor resection (HR = 0.37, <i>p</i> = 0.007) were independent prognostic factors for PFS, similarly to OS. CA19-9 ≤ 200 UI/L (OR = 2.6, <i>p</i> = 0.047) was predictive of the tumor response. Consolidation chemoradiotherapy, more often used in the FFX group (11.7% vs. 50.6%; <i>p</i> < 0.001), was not predictive. Conclusion: This retrospective study did not show any difference between GN and FFX as the first-line treatment in patients with LAPC.https://www.mdpi.com/2072-6694/13/11/2797pancreatic cancerFOLFIRINOXgemcitabine/nab-paclitaxelprognostic factorspredictors of response
spellingShingle Nicolas Williet
Angelica Petrillo
Gaël Roth
Michele Ghidini
Mila Petrova
Julien Forestier
Anthony Lopez
Audrey Thoor
Lucie Weislinger
Ferdinando De Vita
Julien Taieb
Jean Marc Phelip
Gemcitabine/Nab-Paclitaxel versus FOLFIRINOX in Locally Advanced Pancreatic Cancer: A European Multicenter Study
Cancers
pancreatic cancer
FOLFIRINOX
gemcitabine/nab-paclitaxel
prognostic factors
predictors of response
title Gemcitabine/Nab-Paclitaxel versus FOLFIRINOX in Locally Advanced Pancreatic Cancer: A European Multicenter Study
title_full Gemcitabine/Nab-Paclitaxel versus FOLFIRINOX in Locally Advanced Pancreatic Cancer: A European Multicenter Study
title_fullStr Gemcitabine/Nab-Paclitaxel versus FOLFIRINOX in Locally Advanced Pancreatic Cancer: A European Multicenter Study
title_full_unstemmed Gemcitabine/Nab-Paclitaxel versus FOLFIRINOX in Locally Advanced Pancreatic Cancer: A European Multicenter Study
title_short Gemcitabine/Nab-Paclitaxel versus FOLFIRINOX in Locally Advanced Pancreatic Cancer: A European Multicenter Study
title_sort gemcitabine nab paclitaxel versus folfirinox in locally advanced pancreatic cancer a european multicenter study
topic pancreatic cancer
FOLFIRINOX
gemcitabine/nab-paclitaxel
prognostic factors
predictors of response
url https://www.mdpi.com/2072-6694/13/11/2797
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