Multiple myeloma (MM) or plasma cell myeloma (PCM) is a cytogenetically heterogeneous proliferative disorder of clonal plasma cells.The abbreviation "CRAB" denotes the most typical clinical manifestations of MM: hypercalcemia, renal failure, anemia, and lytic bone
lesions. 1The detection of lytic bone lesions distinguishes asymptomatic from symptomatic MM, that requires treatment, even in the absence of clinical symptoms. [2][3][4] Although the radiographic skeletal survey was the standard imaging tool for detecting lytic bone lesions in MM patients for many years, low-dose whole-body CT (LDWBCT) imaging replaced the skeletal survey due to its higher sensitivity and quick and comfortable examination time in most centers. 3,5-7 Due to high-intrinsic bone contrast, the tube current can be significantly lowered (ie, 50-100 mA, depending on the weight of the patient), resulting in a low effective equivalent dose. 8Whole-body MRI (WBMRI) has been shown to have a higher specificity and sensitivity in lesion detection than the radiographic skeletal survey 9,10 and a higher sensitivity than MDCT. 11,12 However, WBMRI has its limitations due to a long acquisition time and availability. 13 MRI shows bone marrow involvement but is not able to detect osteolyses. CT shows osseous lesions as well as bone fractures and allows fracture risk assessment. 14 For these reasons, low-dose whole-body CT has become the most commonly performed imaging modality for MM across many centers.
AbstractObjective: Beta-2-microglobulin is a serum marker of tumor burden in multiple myeloma (MM). Our aim was to correlate serum β₂-microglobulin levels in patients with MM to tumor burden determined by low-dose whole-body CT (LDWBCT).
Materials and Methods:A total of 52 patients with newly diagnosed, untreated MM who underwent LDWBCT were included. LDWBCT scans were assessed by two musculoskeletal radiologists in consensus for focal lesions. The Durie and Salmon PLUS staging system was used for staging patients in stages I-III. β₂-microglobulin was also subdivided into stages I-III on the basis of the multiple myeloma International Staging System (ISS).
Results: Using the Durie and Salmon PLUS staging system criteria for image evaluation, we were able to identify stage I MM in 17 patients, stage II MM in nine patients, and stage III MM in 26 patients. Eight of nine patients with stage II MM and 16 of 26 patients with stage III MM had normal β₂-microglobulin levels. Thus, 24 of 35 patients (68.6%) had 5 or more focal lesions and false-negative β₂-microglobulin levels. Conclusion: Serum β₂-microglobulin levels alone may not indicate the full extent of tumor burden in a significant subset of myeloma patients. K E Y W O R D S multiple myeloma, plasma cell neoplasms How to cite this article: Pfahler V, D'Anastasi M, Dürr H-R, Schinner R, Ricke J, Baur-Melnyk A. Tumor load in patients with multiple myeloma: β₂-microglobulin levels versus lowdose whole-body CT. Eur J Haematol. 2020;104:383-389.