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Induction triplet chemotherapy in patients with rectal adenocarcinoma and synchronous metastases, an AGEO-FFCD study - 20/12/24

Doi : 10.1016/j.clinre.2024.102514 
Victoire Dabout a, , Laurent Mineur b, David Tougeron c, Karine Le Malicot d, Claire Gallois e, Jean Marc Phelip f, Anthony Turpin g, Romain Cohen h, Benedicte Demoustier i, Vincent Hautefeuille j, Christophe Locher k, Charles-Briac Levaché l, Emmanuel Mitry m, Thierry Lecomte n, Fabien Brocard o, Deborah Hassid p, Marie Porte q, Gilles Breysacher r, Jean-Paul Lagasse s, Côme Lepage t , Marine Valéry u, Jean-Baptiste Bachet a,
a Sorbonne University, Hepato-gastroenterology and digestive oncology department, Pitié Salpêtrière hospital, APHP, Paris, 47-83 Boulevard de l'hôpital, Paris 75013, France 
b Department of Radiotherapy and Medical Oncology, Sainte-Catherine Institute, Avignon, France 
c Department of Gastroenterology and Hepatology, Centre Hospitalo-universitaire de Poitiers, Poitiers, France 
d Fédération Francophone de Cancérologie Digestive, Dijon, France 
e Department of Gastroenterology and Digestive Oncology, European Georges Pompidou hospital, Paris, France 
f University Hospital of Saint Etienne, Saint Etienne, France; Unité HESPER EA-7425 Université Jean Monnet/Claude Bernard Lyon 1, France 
g Medical Oncology Department, University hospital, Lille, France and University of Lille, Lille, France 
h Sorbonne University, Department of Oncology, Saint-Antoine Hospital, INSERM 938, SIRIC CURAMUS, Paris, France 
i Univ. Grenoble Alpes / Hepato-Gastroenterology and Digestive Oncology department, CHU Grenoble Alpes / Institute for Advanced Biosciences, CNRS UMR 5309-INSERM U1209, Grenoble, France 
j Departments of Hepatogastroenterology and Digestive Oncology, CHU Amiens Picardie, Amiens, France 
k Department of Hepato-gastroenterology and Digestive Oncology, Meaux Hospital, France 
l Département d'Oncologie Médicale, Clinique Francheville, Périgueux, France 
m Medical Oncology department, Institut Paoli-Calmettes, Marseille, France 
n Department of Hepatogastroenterology and Digestive Oncology, Hôpital Trousseau, CHRU de Tours, 37044 Tours Cedex 09, UMR INSERM U 1069, Université de Tours, 10 Boulevard Tonnellé, Tours 37000, France 
o GINECO and Centre Oncologie de Gentilly, Nancy, France 
p Gastroenterology Department, AP-HP, Hôpital Saint-Louis/Lariboisière, Paris, France 
q Department of Medical Oncology, Centre Hospitalier Universitaire Nantes, Nantes University, Nantes, France 
r Gastroenterology Department, CH Pasteur, Colmar, France 
s Department of Gastroenterology, Hepatology and digestive Oncology, Centre Hospitalo-universitaire d'Orleans, Orleans, France 
t Burgundy Digestive Cancer Registry, INSERM U866, Dijon Cedex 21079, France 
u Medical Oncology Department, Gustave Roussy, Villejuif F-94805, France 

Corresponding authors.

Highlights

-Management of metastatic rectal adenocarcinoma is multidisciplinary and complex.
-Induction triplet chemotherapy is effective on primary site and metastases.
-Induction chemotherapy is associated with a high rate of objective response rate.
Metastases resection allows for prolonged survival.
Prognostic value of KRAS/BRAF mutations appears similar for rectal and colon cancers.

Il testo completo di questo articolo è disponibile in PDF.

Abstract

Aim of the study

The management of synchronous metastatic rectal cancer (SMRC) is complex and multimodal, involving chemotherapy, surgery and/or radiotherapy. The aim of this study was firstly to confirm the efficacy of the induction FOLFIRINOX, and secondly to evaluate the different therapeutic strategies and outcomes of patients.

Patients and methods

This French study combined data from a prospective FFCD trial and a multicenter cohort. Patients included had SMRC and had undergone induction triplet chemotherapy. Two groups of patients were defined according to the resectability of metastases at baseline: resectable (Res) and unresectable (URes). The primary endpoint was the objective response rate.

Results

146 patients were included in 16 French centers and 65 patients in the FFCD1102 trial. In overall population the median age of patients was 59 years, 86% of tumors were of the lower or middle rectum, 33% were well-differentiated, 53% were RAS mutated and 7% BRAF mutated. Triplet induction was associated with 80% of objective response and 92% of disease control. After the induction phase, 69% and 48% of patients of Res and URes groups underwent rectal surgery, and secondary metastases resection was done in 79% and 39% of patients, respectively. Median overall survival (OS) for Res was 56.3 months (95% CI: 22.54-NA). Median OS for URes who had or not secondary metastases resection were 45.1 months (95% CI: 39.89-NA) and 21.1 months (95% CI 17.31–27.1), respectively. Patients with BRAF mutated tumors were more likely to have unresectable disease, and had worse survivals than the patients with RAS mutated or RAS/BRAF wild-type.

Conclusion

Triplet induction chemotherapy is a treatment of choice in selected patients with SMRC, allowing to adapt the therapeutic strategy to the response and invasiveness of the various sites.

Structured abstract

The management of metastatic rectal cancer is essentially based on three main therapeutic approaches: surgery, radiotherapy/chemoradiotherapy and chemotherapy. Induction triplet chemotherapy appears as a good choice for fit and young patients. It allows to adapt the therapeutic strategy to the response and invasiveness of the various sites. In this study dedicated to patients undergoing treatment for rectal cancer with synchronous metastases, FOLFIRINOX-based induction chemotherapy was associated with objective response rate of 77% and disease control rate of 92%. These results are similar with those of the FFCD 1102 trial and confirm the efficacy of induction chemotherapy with FOLFIRINOX with or without targeted therapy in these patients in daily routine practice. Surgery for metastases is a key factor in determining patient's outcome and triplet induction chemotherapy, associated with high response rates, enables a significant percentage of patients to undergo surgery and appears therefore to be a treatment of choice, particularly for patients whose disease is unresectable at baseline.

Il testo completo di questo articolo è disponibile in PDF.

Keywords : Metastatic rectal cancer, Synchronous metastases, FOLFIRINOX, Resectability, KRAS, BRAF


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