This is a study that evaluates the sensitivity of the cardiac uptake of 18F-FDG measured on D28 +/- 7 days, D42 +/- 7 days ou D56 + 4 days of the administration of ATCs to identify at 1 year the patients at risk of occurrence of a LVSD defined by a drop of more than 10 units of the LVEF and LVEF \<53%.
Design : A multicenter clinical trial with 11 sites participating in the study.
Sample size : 484 patients
Duration of inclusion: 37 months Patient observation period: 12 months Total duration: 49 months
Assessment :
There is an inclusion visit, then protocol visits at D28 +/- 7 days, D42 +/- 7 days ou D56 + 4 days, D84 or D126 and at the end of the study (M12).
There is no interim analysis planned. Analyzes will be performed at the end of the test after reviewing the data and freezing the database.
