RSHF in Colorectal Cancer
- Conditions
- Metastatic Colorectal Cancer
- Interventions
- Radiation: RadiationDrug: Irinotecan
- Registration Number
- NCT01220063
- Lead Sponsor
- Institut Cancerologie de l'Ouest
- Brief Summary
The purpose of this study is to study stereotactic radiotherapy with a dose of 40 Gy in 4 fractions over 2 weeks with concomitant 40 mg/m2 of irinotecan (1st and 3rd irradiation session).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 48
-
Age > or = 18 years
-
Social Insurance
-
Performance Index <2
-
Life expectancy> 6 months
-
adenocarcinoma colorectal (histologically proven)
-
Metastases (inoperable or recurrent after surgery),
-
hepatic localization and / or lung (up to 3 if one organ metastasis or 3 in total if the two bodies are metastatic). The largest diameter of the metastasis will < ou = 6cm for the liver, < or = 6 cm for the lung. If multiple metastases, the sum of their maximum diameter is 6cm < ou = the liver, < ou = 6 cm for the lung.
-
Lesion (s) measurable (s) and evaluable (s)
-
CT less than 3 weeks
-
Patients must have received at least one prior chemotherapy regimen containing 5FU
• Patients may have received one or more lines of chemotherapy including irinotecan.
-
bilirubin <1.5 x ULN
-
AST and ALT <5x ULN
-
neutrophils> 1.5x109 / L, platelets> 100x109 / L, hemoglobin> 9 g / dL
-
TP, TCA Normal (only for patients treated with a permanent implant)
-
Informed consent signed.
-
contraindication to the administration of irinotecan.
-
History of radiotherapy in the thoraco-abdominal-cons indicating further irradiation.
-
History of other invasive cancer treated in a period of less than 5 years (basal cell carcinoma and non-invasive cervical excepted)
-
Metastatic disease diffuse or more than three metastases in the liver and / or lung during the natural history of disease (excluding any patient is having a complete radiological response on several metastases although 1-3 residual after treatment ( s) medical (at)).
-
Location (s) tumor (s) = CTV to less than 12 mm laterally or less than 15 mm in the cranio-caudal, stomach, small intestine, esophagus, trachea, bronchi of right and left pulmonary arteries and right and left.
-
Pregnancy or breastfeeding.
- Lack of means or refusal to use effective contraception for men or women of childbearing age.
-
Any other concomitant experimental treatment.
-
Any other concurrent anticancer therapy, immunotherapy or hormonal therapy.
-
Monitoring impossible because of psychological, sociological or because of geographical distance.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Radiation + Irinotecan Irinotecan Irinotecan will be administered : - 40 mg/m² in serum physiologique during 30 to 90 min at D1 and D8 of radiotherapy Radiotherapy (RSHF) will be administered : * at D1, D3, D8 and D10 * 48 Gy, 12 Gy by fractions twice a week Radiation + Irinotecan Radiation Irinotecan will be administered : - 40 mg/m² in serum physiologique during 30 to 90 min at D1 and D8 of radiotherapy Radiotherapy (RSHF) will be administered : * at D1, D3, D8 and D10 * 48 Gy, 12 Gy by fractions twice a week
- Primary Outcome Measures
Name Time Method tumor response accoording to recist criteria 5 years
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (6)
Centre Oscar Lambret
🇫🇷Lille, France
Centre hospitalier Lyon Sud
🇫🇷Lyon, France
Hôpital la Source
🇫🇷Orléans, France
Hôpital Saint André
🇫🇷Bordeaux, France
Centre René Gauducheau
🇫🇷Saint Herblain, France
Centre Léon Berard
🇫🇷Lyon, France