Efficacy and Safety of Aflibercept in Combination With Chemotherapy Beyond Second-Line Therapy in Metastatic Colorectal Carcinoma Patients: An AGEO Multicenter Study.


Journal

Clinical colorectal cancer
ISSN: 1938-0674
Titre abrégé: Clin Colorectal Cancer
Pays: United States
ID NLM: 101120693

Informations de publication

Date de publication:
03 2020
Historique:
received: 14 02 2019
revised: 10 07 2019
accepted: 27 08 2019
pubmed: 28 10 2019
medline: 11 5 2021
entrez: 26 10 2019
Statut: ppublish

Résumé

Although no data have been reported beyond second-line therapy, aflibercept is approved in this setting in many countries. We conducted a multicenter study to analyze the efficacy and safety of a aflibercept-chemotherapy regimen beyond second-line therapy in patients with metastatic colorectal cancer. Metastatic colorectal cancer patients treated with aflibercept beyond second-line therapy were included. Objective response rate, overall survival (OS), and progression-free survival (PFS) were assessed. A total of 130 patients were included. Median OS and PFS were 7.6 months (95% confidence interval, 6.2-9.3) and 3.3 months (95% confidence interval, 2.7-3.8), respectively. The best response rates were partial response 6.9%, stable disease 38.5%, progressive disease 42.5%, and not evaluable 12%. According to whether patients received previous FOLFIRI (leucovorin, 5-fluorouracil, irinotecan, and oxaliplatin)-bevacizumab or not, OS was 7.7 and 8.1 months (P = .31), and PFS was 2.9 and 3.9 months (P = .02), respectively. Interestingly, PFS and OS were both significantly improved by 4% and 5% per month, respectively, without antiangiogenic treatment before the initiation of the aflibercept regimen. The negative effect of prior FOLFIRI-bevacizumab or shorter time since last bevacizumab was maintained in multivariate analysis for both OS and PFS. The aflibercept-chemotherapy regimen is a therapeutic option in patients with chemorefractory disease beyond second-line therapy, in particular in patients with an antiangiogenic-free interval.

Sections du résumé

BACKGROUND
Although no data have been reported beyond second-line therapy, aflibercept is approved in this setting in many countries. We conducted a multicenter study to analyze the efficacy and safety of a aflibercept-chemotherapy regimen beyond second-line therapy in patients with metastatic colorectal cancer.
PATIENTS AND METHODS
Metastatic colorectal cancer patients treated with aflibercept beyond second-line therapy were included. Objective response rate, overall survival (OS), and progression-free survival (PFS) were assessed.
RESULTS
A total of 130 patients were included. Median OS and PFS were 7.6 months (95% confidence interval, 6.2-9.3) and 3.3 months (95% confidence interval, 2.7-3.8), respectively. The best response rates were partial response 6.9%, stable disease 38.5%, progressive disease 42.5%, and not evaluable 12%. According to whether patients received previous FOLFIRI (leucovorin, 5-fluorouracil, irinotecan, and oxaliplatin)-bevacizumab or not, OS was 7.7 and 8.1 months (P = .31), and PFS was 2.9 and 3.9 months (P = .02), respectively. Interestingly, PFS and OS were both significantly improved by 4% and 5% per month, respectively, without antiangiogenic treatment before the initiation of the aflibercept regimen. The negative effect of prior FOLFIRI-bevacizumab or shorter time since last bevacizumab was maintained in multivariate analysis for both OS and PFS.
CONCLUSION
The aflibercept-chemotherapy regimen is a therapeutic option in patients with chemorefractory disease beyond second-line therapy, in particular in patients with an antiangiogenic-free interval.

Identifiants

pubmed: 31648924
pii: S1533-0028(19)30090-8
doi: 10.1016/j.clcc.2019.08.003
pii:
doi:

Substances chimiques

Angiogenesis Inhibitors 0
Recombinant Fusion Proteins 0
aflibercept 15C2VL427D
Bevacizumab 2S9ZZM9Q9V
Receptors, Vascular Endothelial Growth Factor EC 2.7.10.1
Leucovorin Q573I9DVLP
Fluorouracil U3P01618RT
Camptothecin XT3Z54Z28A

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

39-47.e5

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Marie Auvray (M)

Department of Digestive Oncology, European Georges Pompidou Hospital, René Descartes University, Paris, France.

David Tougeron (D)

Department of Hepato-Gastroenterology, Center Hospitalo-Universitaire de Poitiers, Poitiers, France.

Edouard Auclin (E)

Methodology and quality of life unit in oncology, University hospital of Besançon, Besançon, France; University Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, Besançon, France.

Valérie Moulin (V)

Department of Digestive Oncology Center Hospitalier de La Rochelle, La Rochelle, France.

Pascal Artru (P)

Department of Hepato-Gastroenterology, Jean Mermoz Hospital, Lyon, France.

Vincent Hautefeuille (V)

Department of Digestive Oncology, CHU Amiens, Amiens, France.

Pascal Hammel (P)

Department of Digestive Oncology, Beaujon University Hospital, AP-HP and University Paris 7, Denis Diderot, Clichy, France.

Thierry Lecomte (T)

Department of Hepato-Gastroenterology and Digestive Oncology, CHU de Tours, Hôpital Trousseau, Tours, France.

Christophe Locher (C)

Department of Hepato-Gastroenterology, Center Hospitalier de Meaux, Meaux, France.

Gaëlle Sickersen (G)

Department of Hepato-Gastroenterology, CHU Saint-Louis, Paris, France.

Romain Coriat (R)

Department of Hepato-Gastroenterology and Digestive Oncology, CHU Cochin, Paris, France.

Cédric Lecaille (C)

Department of Gastroenterology and Digestive Oncology, Polyclinique de Bordeaux Nord, Bordeaux, France.

Dewi Vernerey (D)

Methodology and quality of life unit in oncology, University hospital of Besançon, Besançon, France.

Julien Taieb (J)

Department of Digestive Oncology, European Georges Pompidou Hospital, René Descartes University, Paris, France.

Simon Pernot (S)

Department of Digestive Oncology, European Georges Pompidou Hospital, René Descartes University, Paris, France. Electronic address: simon.pernot@gmail.com.

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Classifications MeSH