Antibody based positron emission tomography (immuno-PET) imaging is of increasing importance to visualize and characterize tumor lesions. Additionally, it can be used to identify patients who may benefit from a particular therapy and monitor the therapy outcome. In recent years the field is focused on 89 Zr, a radiometal with near ideal physical and chemical properties for immuno-PET. In this review we will discuss the production of 89 Zr, the bioconjugation strategies, and applications in (pre-) clinical studies of 89 Zrbased immuno-PET in oncology. To date, 89 Zr-based PET imaging has been investigated in a wide variety of cancer-related targets. Moreover, clinical studies have shown the feasibility for 89 Zr-based immuno-PET to predict and monitor treatment, which could be used to tailor treatment for the individual patient. Further research should be directed towards the development of standardized and robust conjugation methods and improved chelators to minimize the amount of released Zr 4+ from the antibodies. Additionally, further validation of the imaging method is required. The ongoing development of new 89 Zr-labeled antibodies directed against novel tumor targets is expected to expand applications of 89 Zr-labeled immuno-PET to a valuable method in the medical imaging.