D'Anastasi Melvin, Notohamiprodjo Mike, Schmidt Gerwin P, Dürr Hans-Roland, Reiser Maximilian Ferdinand, Baur-Melnyk Andrea
1 Institute for Clinical Radiology, University Hospitals Munich, Campus Grosshadern, Ludwig-Maximilians-Universität, Marchioninistrasse 15, 81377 Munich, Bayern, Germany.
AJR Am J Roentgenol. 2014 Oct;203(4):854-62. doi: 10.2214/AJR.13.10724.
Beta-2-microglobulin is a serum maker of tumor burden in hematologic malignancies. We aimed to correlate serum β2-microglobulin levels in patients with multiple myeloma (MM) to tumor mass determined by whole-body MRI.
We retrospectively included patients with newly diagnosed, untreated MM who underwent whole-body MRI at our institution between 2003 and 2011. Patients with a glomerular filtration rate of less than 60 mL/min were excluded from analysis because β2-microglobulin levels are increased in renal failure. Thirty patients could be included. Whole-body MRI examinations (T1-weighted turbo spin-echo and STIR sequences) were assessed by two musculoskeletal radiologists in consensus for focal lesions and the presence of diffuse myeloma infiltration. The presence of diffuse infiltration was confirmed by histology as the reference standard. MM was staged according to the Durie and Salmon PLUS staging system.
According to whole-body MRI findings, MM was classified as Durie and Salmon PLUS stage I (low grade) in 13 patients, stage II (intermediate grade) in six patients, and stage III (high grade) in 11 patients. As we expected, most patients with stage I disease (12/13) had normal β2-microglobulin levels (≤ 3 mg/L). Higher β2-microglobulin values were associated with a higher stage of disease (p < 0.05). However, five of six patients with stage II MM and five of 11 patients with stage III MM showed normal β2-microglobulin levels. Thus, 10 of 17 patients (58.8%) with substantial infiltration in the bone marrow showed false-negative β2-microglobulin levels.
Serum β2-microglobulin levels correlate with tumor stage in MM. However, it may be misleading as a marker of tumor load in a subset of patients with substantial myeloma infiltration in the bone marrow. Whole-body MRI may display the full tumor load and correctly show the extension of myeloma infiltrates.
β2微球蛋白是血液系统恶性肿瘤中肿瘤负荷的血清标志物。我们旨在将多发性骨髓瘤(MM)患者的血清β2微球蛋白水平与通过全身MRI确定的肿瘤体积相关联。
我们回顾性纳入了2003年至2011年间在我院接受全身MRI检查的新诊断、未治疗的MM患者。肾小球滤过率低于60 mL/分钟的患者被排除在分析之外,因为肾衰竭时β2微球蛋白水平会升高。共纳入30例患者。两名肌肉骨骼放射科医生共同评估全身MRI检查(T1加权快速自旋回波和短TI反转恢复序列),以确定局灶性病变和弥漫性骨髓瘤浸润情况。以组织学作为参考标准确认弥漫性浸润的存在。MM根据Durie和Salmon PLUS分期系统进行分期。
根据全身MRI检查结果,13例患者的MM被分类为Durie和Salmon PLUS I期(低级别),6例为II期(中级别),11例为III期(高级别)。正如我们所预期的,大多数I期疾病患者(12/13)的β2微球蛋白水平正常(≤3 mg/L)。β2微球蛋白值越高,疾病分期越高(p<0.05)。然而,II期MM的6例患者中有5例以及III期MM的11例患者中有5例的β2微球蛋白水平正常。因此,17例骨髓有大量浸润的患者中有10例(58.8%)的β2微球蛋白水平呈假阴性。
血清β2微球蛋白水平与MM的肿瘤分期相关。然而,对于一部分骨髓有大量骨髓瘤浸润的患者,它作为肿瘤负荷的标志物可能会产生误导。全身MRI可能会显示完整的肿瘤负荷,并正确显示骨髓瘤浸润的范围。