医学
等离子体电池
单克隆抗体
单克隆
蛋白酶体
免疫学
药理学
癌症研究
抗体
生物
细胞生物学
出处
期刊:Primary Care
[Elsevier BV]
日期:2016-10-17
卷期号:43 (4): 677-691
被引量:47
标识
DOI:10.1016/j.pop.2016.07.002
摘要
Plasma cell disorders are benign, premalignant, and malignant conditions characterized by the presence of a monoclonal paraprotein detected in serum or urine. These conditions are biologically, pathologically, and clinically heterogeneous. There have been major advances in the understanding of the biology of these diseases, which are promoting the development of therapies with novel mechanisms of action. Novel agents such as proteasome inhibitors, immunomodulatory drugs, and monoclonal antibodies have gained approval in the United States and Europe for the treatment of plasma cell disorders. Such therapies are translating into higher rates of response and survival and better toxicity profiles.
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