TraStuzumAb-Radiotherapy : Impact on the Cerebral Prevention
- Conditions
- Breast CancerMetastasisSur-expressing Her2-neu
- Interventions
- Radiation: cerebral prophylactic radiationDrug: Other chemotherapy in association with Trastuzumab
- Registration Number
- NCT01613482
- Lead Sponsor
- Centre Oscar Lambret
- Brief Summary
Evaluate the survival without metastasis in patients treated by Trastuzumab in association with other chemotherapies for a breast cancer expressing HER2-NEU.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- Female
- Target Recruitment
- 13
- Patients with breast cancer, expressing HER2-NEU (score +++ in ICH or ++ and amplification on FISH or CISH, SISH)
- Visceral metastasis, only or multiple
- First line metastasis treatment by Trastuzumab in association with chemotherapy
- Good general conditions: OMS=<2 or Karnofsky >=70%
- Age > 18 years and < 70 years
- Life expectancy >=3 mois
- No Trastuzumab since more of 6 months
- No cerebral metastasis (MRI)
- Efficacy contraception for women with genital capacities
- Consent signed by the patient
Exclusion Criteria
- Contraindication to IRM
- Psychiatric decease
- Prior cerebral radiotherapy,
- Geographical constraint, compromising the fallow of patients
- Infectious or other serious pathology, likely to stop the treatment
- Positive serology (HIV, hBC, hBS)
- Inclusion in an other clinical trial or in the 4 weeks before th inclusion
- Pregnant or breastfeeding women
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Arm A Other chemotherapy in association with Trastuzumab Without cerebral prophylactic radiation Arm B cerebral prophylactic radiation With cerebral prophylactic radiation Arm B Other chemotherapy in association with Trastuzumab With cerebral prophylactic radiation Arm B Trastuzumab With cerebral prophylactic radiation Arm A Trastuzumab Without cerebral prophylactic radiation
- Primary Outcome Measures
Name Time Method free of cerebral metastasis survival 5 years
- Secondary Outcome Measures
Name Time Method survival (overall and free visceral progression) 5 years quality of life before treatment, after 3 months, 6 months, 12 months, 24 months, 36 months, 48 months, 60 months Questionnaire QLQ-bn20
evaluate neurological, haemorrhagic, skin toxicities During study weekly during radiotherapy and 2 weeks after radiotherapy
P105 value prior to trastuzumab, after 3 months, 6 months, 12 months, 18 months, 24 months, 36 months Blood sample
neurological toxicities During study * neurological exams
* Cognitive test
* Subjective questionnaire of cognitive complaint
* questionnaire of EORTC QLQ-BN20
Trial Locations
- Locations (26)
Centre Médical de Forcilles
🇫🇷Forcilles-attilly, France
CHU Dupuytren
🇫🇷Limoges, France
Centre Maurice Tubiana
🇫🇷Caen, France
Centre Hospitalier
🇫🇷BOULOGNE Sur Mer, France
Centre G-François Baclesse
🇫🇷Caen, France
Centre Léonard de Vinci
🇫🇷Dechy, France
Clinique des Ormeaux- Vauban
🇫🇷Le Havre, France
Centre Bourgogne
🇫🇷Lille, France
Centre Oscar LAMBRET
🇫🇷Lille, France
Clinique Clinique Clementville
🇫🇷Montpellier, France
Centre Hospitalier de Mulhouse
🇫🇷Mulhouse, France
Centre Azuréen de Cancérologie
🇫🇷Mougins, France
Centre Catherine de Sienne
🇫🇷Nantes, France
Clinique Hartmann
🇫🇷NEUILLY sur SEINE, France
Centre Antoine Lacassagne
🇫🇷Nice, France
Centre médical Oncogard
🇫🇷Nîmes, France
Hôpital Tenon
🇫🇷Paris, France
Centre Catalan d'Oncologie
🇫🇷Perpignan, France
Centre Hospitalier LYON SUD
🇫🇷Pierre-benite, France
Centre René Huguenin
🇫🇷Saint Cloud, France
Centre Etienne DOLET
🇫🇷Saint Nazaire, France
Centre de Cancérologie Paris Nord
🇫🇷Sarcelles, France
Oncorad Garonne
🇫🇷Toulouse, France
Centre Alexis Vautrin
🇫🇷Vandoeuvre-les-nancy, France
Institut Gustave Roussy
🇫🇷Villejuif, France
Centre Paul Papin
🇫🇷Angers, France