“…( Figure 1 ). Already in the advent of PET-MRI, the optimization of scan protocols in accordance to specific patient groups (i.e., children) and disease cohorts (i.e., different tumor entities) has been discussed [ 13 , 14 , 15 , 16 ]. Evidently, considering—the still rather seldom performed—scans with PET radiopharmaceuticals labeled with tracers of longer half-lives, such as Zirconium-89 ( 89 Zr; half-life 3.3 days), well matched to the circulation half-lives of antibodies and thus, potentially suitable for immunotherapy monitoring, the scan duration of PET might exceed the time necessary for the MRI sequences [ 17 , 18 ].…”