Department of Internal Medicine, Hematology and Oncology, University Hospital Brno, Brno, Czech Republic.
Babak Myeloma Group, Department of Pathophysiology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Br J Haematol. 2022 Feb;196(4):954-962. doi: 10.1111/bjh.17925. Epub 2021 Nov 2.
Multiple myeloma (MM) is characterized by malignant plasma cell infiltration of the bone marrow. In extramedullary multiple myeloma (EMD), a subclone of these cells migrates out of the bone marrow. Out of 4 985 MM patients diagnosed between 2005 and 2017 in the Czech Republic, we analyzed 234 secondary EMD patients to clarify risk factors of secondary EMD development. We found younger age [<65 years; odds ratio (OR) 4·38, 95% confidence interval (CI): 2·46-7·80, P < 0·0001], high lactate dehydrogenase (LDH) levels (>5 μkat/l; OR 2·07, 95% CI: 1·51-2·84, P < 0·0001), extensive osteolytic activity (OR 2·21, 95% CI: 1·54-3·15, P < 0·001), and immunoglobulin A (IgA; OR 1·53, 95% CI: 1·11-2·11, P = 0·009) or the non-secretory type of MM (OR 2·83; 95% CI: 1·32-6·04, P = 0·007) at the time of MM diagnosis to be the main risk factors for secondary EMD development. Newly diagnosed MM (NDMM) patients with subsequent EMD had inferior median progression-free (PFS) and overall (OS) survival when compared to NDMM patients without future EMD [mPFS: 13·8 months (95% CI: 11·4-16·3) vs 18·8 months (95% CI: 17·7-19·9), P = 0·006; mOS: 26·7 months (95% CI: 18·1-35·4) vs 58·7 months (95% CI: 54·8-62·6), P < 0·001]. We found that NDMM patients with specific risk factors associated with secondary EMD development have a more aggressive disease course before secondary EMD develops.
多发性骨髓瘤(MM)的特征是恶性浆细胞浸润骨髓。在骨髓外多发性骨髓瘤(EMD)中,这些细胞的亚克隆迁移出骨髓。在 2005 年至 2017 年期间在捷克共和国诊断的 4985 例 MM 患者中,我们分析了 234 例继发性 EMD 患者,以明确继发性 EMD 发展的危险因素。我们发现年龄较小(<65 岁;优势比[OR]4.38,95%置信区间[CI]:2.46-7.80,P<0.0001)、乳酸脱氢酶(LDH)水平较高(>5μkat/l;OR 2.07,95% CI:1.51-2.84,P<0.0001)、广泛的溶骨性活性(OR 2.21,95% CI:1.54-3.15,P<0.001)和免疫球蛋白 A(IgA;OR 1.53,95% CI:1.11-2.11,P=0.009)或非分泌型 MM(OR 2.83;95% CI:1.32-6.04,P=0.007)在 MM 诊断时是继发性 EMD 发展的主要危险因素。与无未来 EMD 的 NDMM 患者相比,随后发生 EMD 的新发 MM(NDMM)患者的无进展生存(PFS)和总生存(OS)更差[中位 mPFS:13.8 个月(95%CI:11.4-16.3)vs 18.8 个月(95%CI:17.7-19.9),P=0.006;mOS:26.7 个月(95%CI:18.1-35.4)vs 58.7 个月(95%CI:54.8-62.6),P<0.001]。我们发现,与继发性 EMD 发展相关的特定危险因素的 NDMM 患者在继发性 EMD 发展之前具有更具侵袭性的疾病过程。