Suppr超能文献

识别发生继发性髓外多发性骨髓瘤高风险的患者。

Identification of patients at high risk of secondary extramedullary multiple myeloma development.

机构信息

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.

出版信息

Br J Haematol. 2022 Feb;196(4):954-962. doi: 10.1111/bjh.17925. Epub 2021 Nov 2.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fad/9297924/999c64cbd8ef/BJH-196-954-g002.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验