医学
破骨细胞
骨病
多发性骨髓瘤
疾病
成骨细胞
临床试验
骨重建
生物信息学
重症监护医学
肿瘤科
癌症研究
骨质疏松症
内科学
生物
体外
受体
生物化学
作者
Roy Heusschen,Joséphine Muller,Elodie Duray,Nadia Withofs,Arnold Bolomsky,Frédéric Baron,Yves Béguin,Eline Menu,Heinz Ludwig,Jo Caers
标识
DOI:10.1080/10428194.2017.1323272
摘要
Multiple myeloma (MM) bone disease is a major cause of morbidity and mortality in MM patients and persists even in patients in remission. This bone disease is caused by an uncoupling of bone remodeling, with increased osteoclast and decreased osteoblast activity and formation, culminating in lytic bone destruction. Bisphosphonates are the current standard of care but new therapies are needed. As the molecular mechanisms controlling MM bone disease are increasingly well understood, new therapeutic targets are extensively explored in the preclinical setting and initial clinical trials with novel compounds now show promising results. In this review, we will provide a comprehensive overview of the biology of MM bone disease, summarize its current clinical management and discuss preclinical and clinical data on next generation therapies.
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