Thalidomide in multiple myeloma - clinical trials and aspects of drug metabolism and toxicity

被引:17
作者
Breitkreutz, Iris [1 ,2 ]
Anderson, Kenneth C. [1 ,2 ]
机构
[1] Harvard Univ, LeBow Inst Myeloma Therapeut, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Jerome Lipper Multiple Myeloma Ctr, Dept Med Oncol, Boston, MA 02115 USA
关键词
clinical trials; multiple myeloma; pharmacodynamics; pharmacokinetics; thalidomide;
D O I
10.1517/17425255.4.7.973
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: After the tragic events in the early 1960s, thalidomide has re-emerged as therapeutic for multiple myeloma (MM). It was first approved for the treatment of erythema nodosum leprosum, and is now under evaluation for hematologic and non-hematologic disorders. Its complex mechanism of action is not fully understood; however extensive preclinical studies in MM have revealed its antiangiogenic and immunomodulatory properties. Objective: in this review, we focus on the importance and toxicity of thalidomide in today's clinical use. Methods: Key preclinical and clinical trials available as well as data on the pharmacokinetics and pharmacodynamics of thalidomide in humans are summarized. Conclusions: Thalidomide is widely used as first-line treatment and in relapsed/refractory MM. The most common side effects are fatigue, constipation and peripheral neuropathy, and careful monitoring is required to avoid fetal exposure.
引用
收藏
页码:973 / 985
页数:13
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