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多发性骨髓瘤中的蛋白酶体抑制剂疗法

Proteasome inhibitor therapy in multiple myeloma.

作者信息

Chauhan Dharminder, Hideshima Teru, Mitsiades Constantine, Richardson Paul, Anderson Kenneth C

机构信息

The Jerome Lipper Multiple Myeloma Center, Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, 44 Binney Street, Boston, Massachusetts 02115, USA.

出版信息

Mol Cancer Ther. 2005 Apr;4(4):686-92. doi: 10.1158/1535-7163.MCT-04-0338.

Abstract

Multiple myeloma remains incurable despite available therapies, and novel therapies that target both tumor cell and bone marrow microenvironment are urgently needed. Preclinical in vitro and in vivo studies show remarkable anti-multiple myeloma activity of the proteasome inhibitor bortezomib/PS-341 even in multiple myeloma cells refractory to multiple prior therapies, including dexamethasone, melphalan, and thalidomide. Based on these findings, the U.S. Food and Drug Administration recently approved the first proteasome inhibitor bortezomib (Velcade), formerly known as PS-341, for the treatment of relapsed/refractory multiple myeloma. Bortezomib therapy has set an outstanding example of translational research in the field of oncology. Genomics and proteomic studies further provide rationale for combining bortezomib with conventional and novel agents to inhibit multiple myeloma growth, overcome drug resistance, reduce attendant toxicity, and improve patient outcome in multiple myeloma.

摘要

尽管有多种可用疗法,但多发性骨髓瘤仍然无法治愈,因此迫切需要针对肿瘤细胞和骨髓微环境的新型疗法。临床前的体外和体内研究表明,蛋白酶体抑制剂硼替佐米/PS-341具有显著的抗多发性骨髓瘤活性,即使在对包括地塞米松、美法仑和沙利度胺在内的多种先前疗法耐药的多发性骨髓瘤细胞中也是如此。基于这些发现,美国食品药品监督管理局最近批准了首个蛋白酶体抑制剂硼替佐米(万珂),其前身为PS-341,用于治疗复发/难治性多发性骨髓瘤。硼替佐米疗法为肿瘤学领域的转化研究树立了杰出典范。基因组学和蛋白质组学研究进一步为硼替佐米与传统及新型药物联合使用提供了理论依据,以抑制多发性骨髓瘤的生长、克服耐药性、降低伴随毒性并改善多发性骨髓瘤患者的预后。

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