Xu Han, Xu Yujie, Wang Mengying, Mao Chunxia, Huang Junxia, Li Tianlan, Gao Yan, Liu Shanshan, Zhou Jingjing, Zhang Yi, Feng Xianqi
Department of Hematology, The Affiliated Hospital of Qingdao University, Qingdao, China.
Institute of Translational Medicine, Medical College, Yangzhou University, Yangzhou, China.
Ther Adv Hematol. 2024 Oct 28;15:20406207241292453. doi: 10.1177/20406207241292453. eCollection 2024.
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.
To evaluate the prognosis of patients with multiple myeloma (MM) complicated with myelofibrosis.
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.
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.
The MM patients without SMF exhibited better treatment response ( < 0.05). Importantly, increasing degrees of myelofibrosis were associated with a significant reduction in median progression-free survival (PFS; < 0.05). MM-SMF patients exhibited significantly shorter median PFS and overall survival (OS; < 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 ( < 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.
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.
继发性骨髓纤维化(SMF)的特征是在原发性疾病基础上纤维组织过度沉积,常导致临床表现被原发性疾病掩盖。不幸的是,目前的分期系统未纳入骨髓纤维化,导致SMF患者可能出现治疗延迟。
评估多发性骨髓瘤(MM)合并骨髓纤维化患者的预后。
本研究纳入了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年世界卫生组织标准将MF严重程度分为0 - 3级。依据国际骨髓瘤工作组(IMWG)标准评估治疗疗效,并使用SPSS进行分析。
无SMF的MM患者表现出更好的治疗反应(<0.05)。重要的是,骨髓纤维化程度增加与无进展生存期(PFS)中位数显著降低相关(<0.05)。MM - SMF患者的PFS中位数和总生存期(OS)显著缩短(<0.05)。在MM - SMF组中,中性粒细胞与淋巴细胞比值>2.39、单核细胞与淋巴细胞比值≤0.18以及血小板与淋巴细胞比值≤61.6与PFS中位数和OS显著降低相关(<0.05)。值得注意的是,基于硼替佐米的方案对MM - SMF患者的预后无显著影响,而基于来那度胺的方案显著延长了OS中位数,但对PFS中位数无显著影响。
骨髓纤维化是预测NDMM患者生存结局的重要预后指标。在新治疗时代,迫切需要探索新的治疗策略以改善多发性骨髓瘤合并骨髓纤维化患者的预后。