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Gemcitabine + Nab-paclitaxel or Gemcitabine alone after FOLFIRINOX failure in patients with metastatic pancreatic adenocarcinoma: a real-world AGEO study.

Authors :
Zaibet, Sonia
Hautefeuille, Vincent
Auclin, Edouard
Lièvre, Astrid
Tougeron, David
Sarabi, Mathieu
Gilabert, Marine
Wasselin, Julie
Edeline, Julien
Artru, Pascal
Bechade, Dominique
Morin, Clémence
Ducoulombier, Agnes
Taieb, Julien
Pernot, Simon
Source :
British Journal of Cancer. Jun2022, Vol. 126 Issue 10, p1394-1400. 7p.
Publication Year :
2022

Abstract

<bold>Background: </bold>Gemcitabine (Gem) alone or with Nab-paclitaxel (Gem-Nab) is used as second-line treatment for metastatic pancreatic adenocarcinoma (mPA) after FOLFIRINOX (FFX) failure; however, no comparative data exist. This study evaluates the efficacy and safety of adding Nab-paclitaxel to Gem for mPA after FFX failure.<bold>Methods: </bold>In this retrospective real-world multicenter study, from 2011 to 2019, patients with mPA receiving Gem-Nab (Gem 1000 mg/m² + Nab 125 mg/m², 3 out of 4 weeks) or Gem alone were included after progression on FFX.<bold>Results: </bold>A total of 427 patients were included. Patients receiving Gem-Nab had more metastatic sites, peritoneal disease and less PS 2 (24% vs. 35%). After median follow-up of 22 months, Gem-Nab was associated with better disease control rate (DCR) (56% vs. 32%; P < 0.001), progression-free survival (PFS) (3.5 vs. 2.3 months; 95% CI: 0.43-0.65) and overall survival (OS) (7.1 vs. 4.7 months; 95% CI: 0.53-0.86). After multivariate analysis, Gem-Nab and PS 0/1 were associated with better OS and PFS. Grade 3/4 toxicity was more frequent with Gem-Nab (44% vs. 29%).<bold>Conclusion: </bold>In this study, Gem-Nab was associated with better DCR, PFS and OS compared with Gem alone in patients with mPA after FFX failure, at the cost of higher toxicity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070920
Volume :
126
Issue :
10
Database :
Academic Search Index
Journal :
British Journal of Cancer
Publication Type :
Academic Journal
Accession number :
156788346
Full Text :
https://doi.org/10.1038/s41416-022-01713-w