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Spots Global Cancer Trial Database for First Line Treatment by FOLFIRINOX for Patients With a Rectum Cancer With Synchronous Non Resectable Metastasis

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Trial Identification

Brief Title: First Line Treatment by FOLFIRINOX for Patients With a Rectum Cancer With Synchronous Non Resectable Metastasis

Official Title: Phase II: First Line Treatment by FOLFIRINOX for Patients With a Rectum Cancer With Synchronous Non Resectable Metastasis

Study ID: NCT01674309

Interventions

FOLFORINOX

Study Description

Brief Summary: The FOLFIRINOX protocol seems a promising protocol as attack treatment of a rectum cancer, with an objective response rate of about 70 %. This phase II is to investigate if this systematic attack chemotherapy could control at the same time the rectal tumor and the synchronous metastasis without compromising secondarily the tumor or the metastasis resection or a radiochemotherapy administration. 1. The main objective of the trial is to investigate the tumoral control rate at 4 months, according to the RECIST criteria (version 1.1). 2. The secondary objectives are: * safety of the treament, * rate of local failure and local complication (occlusion, important bleedings, resistant pains with morphinic treatment, perforation), * survival without local failure (radiological or clinical progression of the rectal cancer or local complication), * rectal tumor response rate (CT scan, MRI and endocopy), * metastasis response rate, * disease free survival after complete resection (of primitive tumor and metastases), * progression free survival (local or distal), * overall survival, quality of life (QLQ-C30 + CR 29).

Detailed Description: The FOLFIRINOX protocol seems a promising protocol as attack treatment of a rectum cancer, with an objective response rate of about 70 %. This phase II is to investigate if this systematic attack chemotherapy could control at the same time the rectal tumor and the synchronous metastasis without compromising secondarily the tumor or the metastasis resection or a radiochemotherapy administration. 1. The main objective of the trial is to investigate the tumoral control rate at 4 months, according to the RECIST criteria (version 1.1). 2. The secondary objectives are: * safety of the treament, * rate of local failure and local complication (occlusion, important bleedings, resistant pains with morphinic treatment, perforation), * survival without local failure (radiological or clinical progression of the rectal cancer or local complication), * rectal tumor response rate (CT scan, MRI and endocopy), * metastasis response rate, * disease free survival after complete resection (of primitive tumor and metastases), * progression free survival (local or distal), * overall survival, quality of life (QLQ-C30 + CR 29). 3. Inclusion and non inclusion criteria 4. Treatment 5. Follow up

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

CHU, Amiens, , France

CHU, Angers, , France

CH, Avignon, , France

CH, Beauvais, , France

CHU, Besançon, , France

Avicennes, Bobigny, , France

CHU - Ht Lévêque, Bordeaux, , France

Institut Bergonie, Bordeaux, , France

CH, Béziers, , France

CHU d'Estaing, Clermont Ferrand, , France

Colmar Ch, Colmar, , France

Centre G.F. Leclerc, Dijon, , France

CHU, Dijon, , France

Polyclinique, Francheville, , France

CHD Vendée, La Roche Sur Yon, , France

Clinique Victor Hugo, Le Mans, , France

CHRU - Hôpital Huriez, Lille, , France

CHU La Timone, Marseille, , France

Ipc - Cac, Marseille, , France

CH Layne, Mont de Marsan, , France

Centre Cahterine de Sienne, Nantes, , France

Polyclinique le Languedoc, Narbonne, , France

CH Georges Menon, Niort, , France

CHR - Gasto, Orléans, , France

AP - HP - Pitié Salpêtrière, Paris, , France

CH, Pau, , France

CH, Perpignan, , France

CHU, Rouen, , France

CH Le Foll, Saint Brieuc, , France

Clinique Armoricaine, Saint Brieuc, , France

Polyclinique Côte Basque Sud, Saint Jean De Luz, , France

CH Robert Morlevat, Semur en Auxois, , France

CAC, Strasbourg, , France

Polyclinique de l'Ormeau, Tarbes, , France

Hôpitaux du Leman, Thonon Les Bains, , France

Clinique Saint Jean du Languedoc, Toulouse, , France

CHRU Trousseau, Tours, , France

Contact Details

Name: Jean-Baptiste BACHET, Dr

Affiliation: CHU de La Pitié Salpetrière - APHP

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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