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FOLFIRI plus BEvacizumab or aFLIbercept after FOLFOX-bevacizumab failure for COlorectal cancer (BEFLICO): An AGEO multicenter study.
Torregrosa, Cécile; Pernot, Simon; Vaflard, Pauline; Perret, Audrey; Tournigand, Christophe; Randrian, Violaine; Doat, Solene; Neuzillet, Cindy; Moulin, Valérie; Stouvenot, Morgane; Roth, Gael; Darbas, Tiffany; Auberger, Benjamin; Godet, Tiphaine; Jaffrelot, Marion; Lambert, Aurélien; Dubreuil, Olivier; Gluszak, Cassandre; Bernard-Tessier, Alice; Turpin, Anthony; Palmieri, Lola-Jade; Bouche, Olivier; Goujon, Gael; Lecomte, Thierry; Sefrioui, David; Locher, Christophe; Grados, Lucien; Gignoux, Pauline; Trager, Stéphanie; Nassif, Elise; Saint, Angélique; Hammel, Pascal; Lecaille, Cédric; Bureau, Mathilde; Perrier, Marine; Botsen, Damien; Bourgeois, Vincent; Taieb, Julien; Auclin, Edouard.
Affiliation
  • Torregrosa C; Gastrointestinal Oncology Department, Hôpital Européen Georges Pompidou, AP-HP, Université de Paris, Paris, France.
  • Pernot S; Medical Oncology, Bergonié Institute, Bordeaux, France.
  • Vaflard P; Medical Oncology Department, Curie Institute, Paris, France.
  • Perret A; Department of Cancer Medicine, Gustave Roussy Cancer Institute, Villejuif, France.
  • Tournigand C; Medical Oncology, Henri Mondor Hospital, Assistance Publique des Hôpitaux de Paris, Paris Est Creteil University, INSERM, Creteil, France.
  • Randrian V; Hepatology and Gastro-enterology Department, University Hospital Center of Poitiers, Poitiers, France.
  • Doat S; Digestive Oncology Department, Pitié-Salpêtrière University Hospital, Assistance Publique des Hôpitaux de Paris, Paris, France.
  • Neuzillet C; Medical Oncology Department, Curie Institute, Versailles Saint-Quentin, Paris Saclay University, Paris, France.
  • Moulin V; Oncology Department, Hospital of La Rochelle, La Rochelle, France.
  • Stouvenot M; Department of Oncology, University Hospital Center of Besançon, Besançon, France.
  • Roth G; Hepato-gastroenterology and Digestive Oncology Unit, University Hospital Center of Grenoble, Grenoble, France.
  • Darbas T; Oncology Department, University Hospital Center of Limoges, Limoges, France.
  • Auberger B; Oncology Department, University Hospital Center of Brest, Brest, France.
  • Godet T; Gastroenterology and Digestive Oncology Department, University Hospital Center of Angers, Angers, France.
  • Jaffrelot M; Digestive Oncology Department, University Hospital Center of Toulouse, Toulouse, France.
  • Lambert A; Medical Oncology Department, Institut de Cancérologie de Lorraine, Nancy, France.
  • Dubreuil O; Medical Oncology Department, Diaconesses-Croix St. Simon Hospital, Paris, France.
  • Gluszak C; Medical Oncology Department, Institut de Cancérologie de l'Ouest, Angers, France.
  • Bernard-Tessier A; Gastroenterology and Digestive Oncology Department, Saint-Antoine Hospital, APHP, Paris, France.
  • Turpin A; Department of Medical Oncology, Lille University Hospital, University of Lille, CNRS UMR9020, Inserm UMR-S 1277-Canther-Cancer Heterogeneity, Plasticity and Resistance to Therapies, Lille, France.
  • Palmieri LJ; Gastroenterology and Digestive Oncology Department, Cochin Hospital, APHP, Paris, France.
  • Bouche O; Oncology Department, University Hospital Center of Reims, Reims, France.
  • Goujon G; Gastroenterology and Digestive Oncology Department, Bichat Hospital, Paris, France.
  • Lecomte T; Department of Hepato-Gastroenterology and Digestive Oncology, Tours University Hospital and INSERM U1069 Nutrition, Croissance et Cancer, University of Tours, Tours, France.
  • Sefrioui D; Normandy Centre for Genomic and Personalized Medicine and Department of Hepatogastroenterology, Normandie University, UNIROUEN, Inserm U1245, IRON Group, Rouen University Hospital, Rouen, France.
  • Locher C; Gastroenterology and Digestive Oncology Department, Meaux Hospital, Meaux, France.
  • Grados L; Gastroenterology and Digestive Oncology Department, University Hospital Center of Amiens, Amiens, France.
  • Gignoux P; Oncology Department, University Hospital Center of Martinique, Fort de France, France.
  • Trager S; Medical Oncology Department, Clinic of Stains, Stains, France.
  • Nassif E; Oncology Department, Leon Berard Institute, Lyon, France.
  • Saint A; Medical Oncology Department, Antoine Lacassagne Center, Nice, France.
  • Hammel P; Digestive and Medical Oncology Department, University Paris-Saclay, Hospital Paul Brousse AP-HP, Villejuif, France.
  • Lecaille C; Gastroenterology Department, Polyclinique Bordeaux Nord Aquitaine, Bordeaux, France.
  • Bureau M; Digestive Oncology Department, University Hospital Center of Nantes, Nantes, France.
  • Perrier M; Oncology Department, University Hospital Center of Reims, Reims, France.
  • Botsen D; Oncology Department, University Hospital Center of Reims, Reims, France.
  • Bourgeois V; Gastroenterology and Digestive Oncology Department, Boulogne-Sur-Mer Hospital, Boulogne-Sur-Mer, France.
  • Taieb J; Gastrointestinal Oncology Department, Hôpital Européen Georges Pompidou, AP-HP, Université de Paris, Paris, France.
  • Auclin E; Gastrointestinal Oncology Department, Hôpital Européen Georges Pompidou, AP-HP, Université de Paris, Paris, France.
Int J Cancer ; 151(11): 1978-1988, 2022 Dec 01.
Article in En | MEDLINE | ID: mdl-35833561
After failure of first line FOLFOX-bevacizumab for metastatic colorectal cancer (mCRC), adding either bevacizumab or aflibercept to second-line FOLFIRI increases survival compared to FOLFIRI alone. In this French retrospective multicentre cohort, we included patients with a mCRC treated with either FOLFIRI-aflibercept or FOLFIRI-bevacizumab. The primary endpoint was overall survival (OS), and secondary endpoints were progression-free survival (PFS), disease control rate (DCR: CR + PR + SD) and safety. We included 681 patients from 36 centers, 326 and 355 in the aflibercept and bevacizumab groups, respectively. Median age was 64.2 years and 45.2% of patients were men. Most patients had RAS-mutated tumors (80.8%) and synchronous metastases (85.7%). After a median follow up of 31.2 months, median OS was 13.0 months (95% CI: 11.3-14.7) and 10.4 months (95% CI: 8.8-11.4) in the bevacizumab and aflibercept groups, respectively (P < .0001). Median PFS was 6.0 months (95% CI: 5.4-6.5) and 5.1 months (95% CI: 4.3-5.6) (P < .0001). After adjustment on age, PS, PFS of first line, primary tumor resection, metastasis location and RAS/BRAF status, bevacizumab was still associated with better OS (HR: 0.71, 95% CI: 0.59-0.86, P = .0003). FOLFIRI-bevacizumab combination was associated with longer OS and PFS, and a better tolerability, as compared to FOLFIRI-aflibercept after progression on FOLFOX-bevacizumab.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Camptothecin / Colorectal Neoplasms Type of study: Clinical_trials Limits: Female / Humans / Male / Middle aged Language: En Journal: Int J Cancer Year: 2022 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Camptothecin / Colorectal Neoplasms Type of study: Clinical_trials Limits: Female / Humans / Male / Middle aged Language: En Journal: Int J Cancer Year: 2022 Document type: Article Affiliation country: Country of publication: