Clinical features and treatment of newly diagnosed multiple myeloma with secondary myelofibrosis: a retrospective study.

IF 3.4 3区 医学 Q2 HEMATOLOGY Therapeutic Advances in Hematology Pub Date : 2024-10-28 eCollection Date: 2024-01-01 DOI:10.1177/20406207241292453
Han Xu, Yujie Xu, Mengying Wang, Chunxia Mao, Junxia Huang, Tianlan Li, Yan Gao, Shanshan Liu, Jingjing Zhou, Yi Zhang, Xianqi Feng
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Abstract

Background: Secondary myelofibrosis (SMF) is characterized by the excessive deposition of fibrous tissue on top of the primary disease, often causing clinical manifestations to be overshadowed by the primary disease. Unfortunately, current staging systems do not incorporate myelofibrosis, leading to potential treatment delays for SMF.

Objectives: To evaluate the prognosis of patients with multiple myeloma (MM) complicated with myelofibrosis.

Design: The study included the clinical data and treatment results of 208 newly diagnosed multiple myeloma (NDMM) patients who were treated in the Affiliated Hospital of Qingdao University from January 2014 to August 2020, and performed a retrospective analysis.

Methods: All patients underwent bone marrow biopsy, and MF severity was classified into grades 0-3 according to the 2016 WHO criteria. Treatment efficacy was evaluated based on the International Myeloma Working Group (IMWG) standard and SPSS was used for analysis.

Results: The MM patients without SMF exhibited better treatment response (p < 0.05). Importantly, increasing degrees of myelofibrosis were associated with a significant reduction in median progression-free survival (PFS; p < 0.05). MM-SMF patients exhibited significantly shorter median PFS and overall survival (OS; p < 0.05). In the MM-SMF group, neutrophil-lymphocyte ratio >2.39, monocyte-lymphocyte ratio ⩽0.18, and platelet-lymphocyte ratio ⩽61.6 were associated with significantly reduced median PFS and OS (p < 0.05). Notably, the use of bortezomib-based regimens did not significantly impact prognosis in MM-SMF patients, while lenalidomide-based regimens significantly extended median OS but did not significantly affect median PFS.

Conclusion: Myelofibrosis emerges as an important prognostic indicator for predicting the survival outcomes of NDMM patients. In the era of new therapeutics, there is a pressing need to explore novel treatment strategies in order to improve the prognosis of patients with multiple myeloma complicated by myelofibrosis.

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新诊断多发性骨髓瘤合并继发性骨髓纤维化的临床特征和治疗:一项回顾性研究。
背景:继发性骨髓纤维化(SMF)的特点是纤维组织过度沉积在原发性疾病之上,常常导致临床表现被原发性疾病所掩盖。遗憾的是,目前的分期系统并未将骨髓纤维化纳入其中,这可能导致骨髓纤维化的治疗延误:评估并发骨髓纤维化的多发性骨髓瘤(MM)患者的预后:研究纳入2014年1月至2020年8月在青岛大学附属医院接受治疗的208例新诊断多发性骨髓瘤(NDMM)患者的临床资料和治疗结果,并进行回顾性分析:所有患者均接受骨髓活检,根据2016年WHO标准将骨髓瘤严重程度分为0-3级。根据国际骨髓瘤工作组(IMWG)标准评估疗效,并使用SPSS进行分析:没有SMF的MM患者表现出更好的治疗反应(p p p 2.39),单核细胞-淋巴细胞比值⩽0.18和血小板-淋巴细胞比值⩽61.6与中位PFS和OS显著降低有关(p 结论:SMF是骨髓纤维化的一种表现形式:骨髓纤维化是预测 NDMM 患者生存结果的一个重要预后指标。在新疗法时代,迫切需要探索新的治疗策略,以改善并发骨髓纤维化的多发性骨髓瘤患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
54
审稿时长
7 weeks
期刊介绍: Therapeutic Advances in Hematology delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of hematology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in hematology, providing a forum in print and online for publishing the highest quality articles in this area.
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