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).
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
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
65
INTRAVENOUS administration
CHU
Amiens, France
CHU
Angers, France
CH
Avignon, France
CH
Beauvais, France
CHU
Besançon, France
CH
Béziers, France
Avicennes
Bobigny, France
CHU - Ht Lévêque
Bordeaux, France
Institut Bergonie
Bordeaux, France
CHU d'Estaing
Clermont-Ferrand, France
...and 27 more locations
Tumor control rate of the primary tumor and metastasis
The tumor control rate of the primary site and metastasis is defined as Complete response or Partial response or stability according to RECIST 1.1 criteria
Time frame: 4 months
Toxicity of the treatment
Number of patients presenting the main toxicities during the study
Time frame: Up to 4 months after Last Patient First Visit
rate of local failure and local complication (occlusion, important bleedings, resistant pains with morphinic treatment, perforation)
The rate is defined as the clinical progression or a radiological progression of the rectum cancer or a local complication due to the treatment or due to the progression
Time frame: 4 months
survival without local failure (radiological or clinical progression of the rectal cancer or local complication)
The survival time is defined as the time between the patient's inclusion and the time of the local failure or patient's death
Time frame: Up to 4 months after Last Patient First Visit
rectal tumor response rate (CT scan, MRI and endocopy)
The rectal tumor response rate is the Complete response or the Partial response of the rectal tumor using RECIST 1.1 criteria
Time frame: 4 months
metastasis response rate
The metastasis tumor response rate is the Complete response or the Partial response of metastasis using RECIST 1.1 criteria
Time frame: 4 months
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