Management of bone disease in multiple myeloma

被引:80
作者
Terpos, Evangelos [1 ]
Berenson, James [2 ]
Raje, Noopur [3 ]
Roodman, G. David [4 ]
机构
[1] Natl & Kapodistrian Univ Athens, Dept Clin Therapeut, Sch Med, Alexandra Gen Hosp, Athens 11528, Greece
[2] Inst Myeloma & Bone Res, West Hollywood, CA USA
[3] Massachusetts Gen Hosp, Ctr Canc, Ctr Multiple Myeloma, Boston, MA USA
[4] Indiana Univ Sch Med, Indianapolis, IN 46202 USA
关键词
activin-A; bisphosphonates; bone disease; denosumab; RANKL; sclerostin; sotatercept; Wnt pathway; SKELETAL-RELATED EVENTS; ZOLEDRONIC ACID; DOUBLE-BLIND; ACTIVIN-A; KAPPA-B; RECEPTOR ACTIVATOR; INHIBITS OSTEOCLASTOGENESIS; ALKALINE-PHOSPHATASE; OSTEOLYTIC LESIONS; RESORPTION MARKERS;
D O I
10.1586/17474086.2013.874943
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Osteolytic bone disease is the most common complication of multiple myeloma, resulting in skeletal complications that cause significant morbidity and mortality. Currently, bisphosphonates (BPs) are the mainstay for the treatment of myeloma bone disease. Zoledronic acid which has been found to be superior to clodronate, both in terms of reduction of skeletal-related events (SREs) and survival, and pamidronate are used for the management of myeloma-related bone disease. Patients with active disease (not in CR or VGPR) should receive BPs (especially zoledronic acid) even after two years of administration. Radiotherapy and surgical interventions can also be used for specific conditions, such as pathological fractures, spinal cord compression or uncontrolled pain. The better understanding of the biology of myeloma bone disease has led to the production of several novel agents, such as denosumab (targeting RANKL), sotatercept (activin-A antagonist) and romosozumab (targeting sclerostin) that appear very promising and have entered to clinical development.
引用
收藏
页码:113 / 125
页数:13
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