This study therefore aims to assess current treatment recommended by scientific societies \[ 6-13 \] , brain MRI with injection of contrast for the diagnosis and monitoring of brain metastases . The recommended dose of this examination gadolinium is from 0.1 to 0.3 mmol / kg \[ 14 \] . Sequences infusion different from one center to the other made : some use the infusion T1, other infusion T2 \* . No recommendation establishes whether it is preferable to use one or the other of these sequences. No examination is added for the purposes of protocol. Indications for MRI and the number and timing of MRI checks under this protocol are consistent with what is done in practice . The used type of gadolinium and the injected dose will be identical for both sequences infusion . The assessment shall not in any case the contrast but the interpretation of the sequence itself. Special procedures monitoring implemented embodiment correspond to the two sequences instead of infusion (one of T1-weighted and T2 \* in the other ) , in the original MRI and MRI of the first control , in order to compare their effectiveness
Eligibility criteria: * Major Patients * Addressed MRI for initial assessment of brain metastases * At a suspicion of one or more brain metastases in the brain scanner routine screening * Follow for lung cancer histologically documented * In the Thoracic Oncology Service Professor Lafitte (contact: Dr Cortot) * To whom treatment with chemotherapy or targeted therapy (including anti-angiogenic) is considered * Be socially insured Main Outcomes measures: Comparing the area under the ROC curve of different parameters evaluated in T1 and T2 \* perfusion during the initial assessment for the diagnosis of maximal tumor response evaluated at 1 year
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
30
MRI
Hopital Salengro CHRU de Lille
Lille, France
Comparing different parameters evaluated in T1 and T2 * perfusion
Comparing the area under the ROC curve of different parameters evaluated in T1 and T2 \* perfusion during the initial assessment for the diagnosis of maximal tumor
Time frame: 3 years
Evaluation tumor response
Comparison of the area under the ROC curve of the change in the first control of the various parameters measured in T1 and T2 \* infusion, for the diagnosis of maximum tumor response evaluated at 1 year
Time frame: 1 year
Radiological progression-free survival
Comparison of the ability of the two sequences to predict infusion:
Time frame: 1 year
Survival without neurological signs
Comparison of the ability of the two sequences to predict infusion:
Time frame: 1 year
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