Multicenter, observational, prospective, study. All patients will be treated and monitored according to the local clinical practice. No additional procedures/patient visits in comparison with the usual clinical practice are planned for the study.
Patients candidate to WB-MRI according to clinical practice belonging to the study groups listed above.
Participant is willing and able to give informed consent for participation in the study.
Male or Female, aged ≥ 18 years.
Life expectancy greater than 3 months.
Patients with MRI-unsafe prostheses and devices.
Patients whose tests are of suboptimal quality, or whose test has been suspended, or is incomplete.
Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCS
Lead sponsor