A dvances in therapeutics that improve outcomes of patients with myeloma are key drivers for imaging developments. If bone marrow disease is detected early, and patients are treated according to clinical risk, then survival advantages are conferred (1-8). Histologic confirmation of clonal bone marrow plasma cells of greater than 10% in bone marrow or biopsy-proven plasmacytoma is a core requirement of diagnosis that is related to disease burden. However, for a diagnosis of multiple myeloma requiring treatment, biopsy results must be supplemented with evidence of a myeloma-defining event (hypercalcemia, renal failure, anemia, or bone disease) or a biomarker of malignancy (clonal marrow plasma cell percentage 60%, involved:uninvolved serum free light chain ratio 100, or a positive finding at MRI) (9). Although the International Myeloma Working Group (IMWG) recommends a range of imaging investigations for bone disease (including low-dose CT, fluorine 18 [ 18 F] fluorodeoxyglucose [FDG] PET/CT, and MRI), the high sensitivity of whole-body (WB) MRI is recognized (10,11), and it is recommended for all patients suspected of having myeloma and who underwent low-dose WB CT or FDG PET/CT with negative findings (12). The IMWG definition of bone involvement as a myeloma-defining event remains the presence of more This copy is for personal use only. To order printed copies, contact