免疫调节药物对多发性骨髓瘤患者骨代谢的影响。

IF 2.3 4区 医学 Q2 HEMATOLOGY
Expert Review of Hematology Pub Date : 2024-01-01 Epub Date: 2024-02-12 DOI:10.1080/17474086.2024.2316090
Yang Liu, Bo Li, Xiaomin Chen, Hao Xiong, Chunlan Huang
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引用次数: 0

摘要

简介:免疫调节药物(IMiDs免疫调节药物(IMiDs)被广泛用于治疗新诊断和复发/难治性多发性骨髓瘤患者。这些药物对骨髓瘤骨病(MBD)有潜在影响,包括抑制破骨细胞活性和影响成骨细胞分化。目前尚不确定这些影响是否是直接的,当与蛋白酶体抑制剂联合使用时,可能会对骨形成标志物产生影响:本综述总结了有关 IMiDs 在微环境调节中的作用以及对骨代谢的潜在影响的现有证据。文献检索方法包括使用医学主题词在PubMed上检索基础和临床试验。本综述的共同作者对纳入的文章进行了筛选和评估:作为一种治疗选择,IMiDs可直接影响前成骨细胞/破骨细胞的分化。蛋白酶体抑制剂的联合使用可能会抵消成骨活性标志物的短期上调,因此建议静脉注射唑来膦酸,然而,获得更显著的骨髓瘤反应将对骨髓瘤骨病产生长期的积极影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of immunomodulatory drugs on bone metabolism of patients with multiple myeloma.

Introduction: Immunomodulatory drugs (IMiDs) are widely used in the management of newly diagnosed and relapsed/refractory multiple myeloma patients. These agents show their potential effect on myeloma bone disease (MBD), including inhibition of osteoclasts activity and effects on osteoblasts differentiation. It is unclear whether these effects are direct, which may have an impact on bone formation markers when combined with proteasome inhibitors.

Areas covered: This review summarizes the available evidence on the role of IMiDs in microenvironment regulation and their potential effects on bone metabolism. The literature search methodology consisted of searching PubMed for basic and clinical trials using medical subject terms. Included articles were screened and evaluated by the coauthors of this review.

Expert opinion: As a therapeutic option, IMiDs directly affect preosteoblast/osteoclast differentiation. The combination of proteasome inhibitors may counteract the short-term up-regulation of osteogenic activity markers, and therefore intravenous zoledronic acid is recommended, however, obtaining a more significant myeloma response will have a long-term positive impact on myeloma bone disease.

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来源期刊
CiteScore
4.70
自引率
3.60%
发文量
98
审稿时长
6-12 weeks
期刊介绍: Advanced molecular research techniques have transformed hematology in recent years. With improved understanding of hematologic diseases, we now have the opportunity to research and evaluate new biological therapies, new drugs and drug combinations, new treatment schedules and novel approaches including stem cell transplantation. We can also expect proteomics, molecular genetics and biomarker research to facilitate new diagnostic approaches and the identification of appropriate therapies. Further advances in our knowledge regarding the formation and function of blood cells and blood-forming tissues should ensue, and it will be a major challenge for hematologists to adopt these new paradigms and develop integrated strategies to define the best possible patient care. Expert Review of Hematology (1747-4086) puts these advances in context and explores how they will translate directly into clinical practice.
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