Phase
Condition
Colon Cancer; Rectal Cancer
Colorectal Cancer
Digestive System Neoplasms
Treatment
25 Gy
50 Gy
Capecitabine
Clinical Study ID
Ages > 75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patient ≥75 years
- Eastern Cooperative Oncology Group (ECOG) ≤2
- Adenocarcinoma of the rectum histologically proven
- Tumor ≤12 cm from the anal margin, the measurement done by rigid rectoscopy or by subperitoneal MRI
- Require a pre-operative treatment (tumor classified T3 or T4 resectable by MRI andtomodensitometry or T2 of the very low rectum)
- Patient operable
- No radiologically detectable metastases
- Absolute Neutrophile count (ANC) ≥1500/mm³; Platelets ≥100 000/mm³ and Hemoglobin ≥10g/dL
- Bilirubin ≤1.5 x upper limit of normal (ULN), aspartate aminotransferase (ASAT) andalanine aminotransferase (ALAT) ≤1.5 x upper limit of normal (ULN), AlkalinePhosphatase ≤1.5 x upper limit of normal (ULN)
- Creatinine clearance ≥30 ml/min (Cockcroft and Gault)
- Uracilemia < 16ng/mL
- Public or private Health Insurance coverage
- Patient has been informed and signed the informed consent document
Exclusion
Exclusion Criteria:
- Non-resectable tumor
- History of chronic diarrhea or an inflammatory disease of the colon or rectum, orintestinal obstruction or sub-obstruction
- History of pelvic radiotherapy
- Any active febrile infection or any other serious underlying pathology that mayprevent the patient from receiving the treatment
- Significant Cardiovascular diseases such as, but not limited to: cardiovascular ormyocardial infarction ≤6 months before inclusion, congestive heart failure class II orhigher (NYHA), unstable angina, arrhythmia requiring medication or uncontrolledhypertension;
- Significative cardiovascular conditions such as, but not limited to : Cardiacangioplasty or stenting, Myocardial infarction, Unstable angina, Coronary arterybypass graft surgery Symptomatic peripheral vascular disease, Class III or IVcongestive heart failure, as defined by the New York Heart Association (NYHA),clinically significant irregular heartbeat requiring medication
- Severe and unexpected reactions to fluoropyrimidine therapy
- Any contra-indication to capecitabine and its excipients; patients with hereditaryproblems of galactose intolerance, the Lapp lactase deficiency or glucose-galactosemalabsorption should not included.
- Uracilemia ≥ 16ng/mL
- Any other concomitant cancer or history of cancer in the last 3 years, with theexception of the in situ cancer of the uterus, treated, or squamous-cell or basal-cellcarcinoma.
- Patients already included in another therapeutic trail with an experimental molecule
- Person deprived of liberty
- Patient that for geographical, social and/or physical reasons will not be able tofollow the procedure as required by the protocol
Study Design
Study Description
Connect with a study center
Centre Hospitalier d'Abbeville
Abbeville,
FranceSite Not Available
Clinique Claude Bernard
Albi,
FranceSite Not Available
CHU Amiens Picardie
Amiens,
FranceSite Not Available
Polyclinique Maymard
Bastia,
FranceSite Not Available
Centre Hospitalier de Beauvais
Beauvais, 60021
FranceSite Not Available
CHU de Besançon
Besancon,
FranceSite Not Available
Cebtre Hospitalier de Blois
Blois,
FranceSite Not Available
Hôpital Avicenne
Bobigny,
FranceSite Not Available
Institut Bergonié
Bordeaux,
FranceSite Not Available
Centre François Baclesse
Caen,
FranceSite Not Available
CHU Henri Mondor
Créteil,
FranceSite Not Available
Centre Hospitalier de Dax
Dax,
FranceSite Not Available
CHU DIJON (Hôpital du Bocage)
Dijon,
FranceSite Not Available
Centre Georges François Leclerc
Dijon,
FranceSite Not Available
CHIC des Alpes du Sud- site de Gap
GAP,
FranceSite Not Available
CHU de Grenoble Hôpital A Michallon
Grenoble,
FranceSite Not Available
Hôpital Privé Sainte Marguerite
Hyeres,
FranceSite Not Available
CHD de Vendée
La Roche-sur-yon,
FranceSite Not Available
Institut Hospitalier Franco-Britannique
Levallois-perret,
FranceSite Not Available
Centre Hospitalier Universitaire de Limoges
Limoges,
FranceSite Not Available
Centre Léon Bérard
Lyon,
FranceSite Not Available
Hôpital privé Jean Mermoz
Lyon,
FranceSite Not Available
CHU Timone
Marseille,
FranceSite Not Available
Institut Paoli Calmettes
Marseille,
FranceSite Not Available
Centre azuréen de cancérologie
Mougins,
FranceSite Not Available
Hôpital Américain de Paris
Neuilly-sur-seine,
FranceSite Not Available
Centre Antoine Lacassagne
Nice,
FranceSite Not Available
Chu Caremeau
Nimes,
FranceSite Not Available
Centre Médical Oncogard Institut de cancérologie du Gard
Nîmes,
FranceSite Not Available
Hôpital TENON
Paris,
FranceSite Not Available
CHU de Bordeaux
Pessac,
FranceSite Not Available
Centre Hospitalier Annecy Genevois
Pringy,
FranceSite Not Available
Centre Henri Becquerel
Rouen,
FranceSite Not Available
Hôpital d'instruction des Armées
Saint Mande,
FranceSite Not Available
Clinique Pasteur
Toulouse,
FranceSite Not Available
Institut de Cancérologie de Lorraine
Vandoeuvre Les Nancy,
FranceSite Not Available
Gustave Roussy Cancer Campus Grand Paris
Villejuif,
FranceSite Not Available
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