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TraStuzumAb-Radiotherapy : Impact on the Cerebral Prevention

Phase 3
Terminated
Conditions
Breast Cancer
Metastasis
Sur-expressing Her2-neu
Interventions
Radiation: cerebral prophylactic radiation
Drug: 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
Inclusion Criteria
  • 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
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Arm AOther chemotherapy in association with TrastuzumabWithout cerebral prophylactic radiation
Arm Bcerebral prophylactic radiationWith cerebral prophylactic radiation
Arm BOther chemotherapy in association with TrastuzumabWith cerebral prophylactic radiation
Arm BTrastuzumabWith cerebral prophylactic radiation
Arm ATrastuzumabWithout cerebral prophylactic radiation
Primary Outcome Measures
NameTimeMethod
free of cerebral metastasis survival5 years
Secondary Outcome Measures
NameTimeMethod
survival (overall and free visceral progression)5 years
quality of lifebefore treatment, after 3 months, 6 months, 12 months, 24 months, 36 months, 48 months, 60 months

Questionnaire QLQ-bn20

evaluate neurological, haemorrhagic, skin toxicitiesDuring study

weekly during radiotherapy and 2 weeks after radiotherapy

P105 valueprior to trastuzumab, after 3 months, 6 months, 12 months, 18 months, 24 months, 36 months

Blood sample

neurological toxicitiesDuring 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

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