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Role of FOLFIRINOX and chemoradiotherapy in locally advanced and borderline resectable pancreatic adenocarcinoma: update of the AGEO cohort.
Auclin, Edouard; Marthey, Lysiane; Abdallah, Raef; Mas, Léo; Francois, Eric; Saint, Angélique; Cunha, Antonio Sa; Vienot, Angélique; Lecomte, Thierry; Hautefeuille, Vincent; de La Fouchardière, Christelle; Sarabi, Matthieu; Ksontini, Feryel; Forestier, Julien; Coriat, Romain; Fabiano, Emmanuelle; Leroy, Florence; Williet, Nicolas; Bachet, Jean-Baptiste; Tougeron, David; Taieb, Julien.
Afiliación
  • Auclin E; Department of Hepato-Gastroenterology and Gastrointestinal Oncology, Université de Paris, Paris Descartes University, Hôpital Européen Georges Pompidou, Paris, France.
  • Marthey L; Department of Medical and Thoracic Oncology, Université de Paris, Hôpital Européen Georges Pompidou, Paris, France.
  • Abdallah R; Department of Gastroenterology, Kremlin Bicêtre Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris Sud University, Le Kremlin Bicêtre, France.
  • Mas L; Department of Gastroenterology, Kremlin Bicêtre Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris Sud University, Le Kremlin Bicêtre, France.
  • Francois E; Department of Gastroenterology, La Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Saint A; Department of Oncology, Anticancer Center A Lacassagne, Nice, France.
  • Cunha AS; Department of Oncology, Anticancer Center A Lacassagne, Nice, France.
  • Vienot A; Department of Digestive Surgery, Hôpital Paul Brousse, Villejuif, France.
  • Lecomte T; Department of Oncology, Besançon University Hospital, Besançon, France.
  • Hautefeuille V; Department of Hepato-Gastroenterology and Digestive Oncology, University Hospital Trousseau, Tours, France.
  • de La Fouchardière C; Department of Gastroenterology and Digestive Oncology, Amiens University Hospital, Amiens, France.
  • Sarabi M; Department of Gastrointestinal Oncology, Centre Léon Bérard, Lyon, France.
  • Ksontini F; Department of Gastrointestinal Oncology, Centre Léon Bérard, Lyon, France.
  • Forestier J; Department of Oncology, Institute Salah-Azaïz, Tunis, Tunisia.
  • Coriat R; Department of Gastroenterology, Hôpital Edouard Herriot, Lyon, France.
  • Fabiano E; Department of Gastroenterology, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Leroy F; Department of Radiotherapy, Université de Paris, Hôpital Européen Georges Pompidou, Paris, France.
  • Williet N; Department of GI Oncology, Institut Gustave Roussy, Villejuif, France.
  • Bachet JB; Department of Gastroenterology, University Hospital of Saint-Etienne, Saint-Etienne, France.
  • Tougeron D; Department of Gastroenterology, La Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Taieb J; Department of Hepato-Gastroenterology, Poitiers University Hospital, University of Poitiers, Poitiers, France.
Br J Cancer ; 124(12): 1941-1948, 2021 06.
Article en En | MEDLINE | ID: mdl-33772154
ABSTRACT

BACKGROUND:

FOLFIRINOX has shown promising results in locally advanced (LAPA) or borderline resectable (BRPA) pancreatic adenocarcinoma. We report here a cohort of patients treated with this regimen from the AGEO group.

METHODS:

This is a retrospective multicentre study. We included all consecutive patients with non-pre-treated LAPA or BRPA treated with FOLFIRINOX.

RESULTS:

We included 330 patients (57.9% male, 65.4% <65 years, 96.4% PS <2). Disease was classified as BRPA in 31.1% or LAPA in 68.9%. Objective response rate with FOLFIRINOX was 29.5% and stable disease 51%. Subsequent CRT was performed in 46.4% of patients and 23.9% had curative intent surgery. Resection rates were 42.1% for BRPA and 15.5% for LAPA. Main G3/4 toxicities were fatigue (15%), neutropenia (12%) and neuropathy (G2/3 35%). After a median follow-up of 26.7 months, median OS (mOS) and PFS were 21.4 and 12.4 months, respectively. For patients treated by FOLFIRINOX alone, or FOLFIRINOX followed by CRT, or FOLFIRINOX + /- CRT + surgery, mOS was 16.8 months, 21.8 months and not reached, respectively (p < 0.0001).

CONCLUSIONS:

FOLFIRINOX for LAPA and BRPA seems to be effective with a manageable toxicity profile. These promising results in "real-life" patients now have to be confirmed in a Phase 3 randomised trial.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Adenocarcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Quimioradioterapia Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Br J Cancer Año: 2021 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Adenocarcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Quimioradioterapia Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Br J Cancer Año: 2021 Tipo del documento: Article País de afiliación: Francia