James Cancer Hospital and Solove Research Institute & The Ohio State University, Columbus, OH 43210, USA.
Expert Rev Anticancer Ther. 2013 Mar;13(3):339-58. doi: 10.1586/era.13.9.
Proteasome inhibition has been shown to be an effective strategy for the treatment of multiple myeloma, as demonstrated by the clinical activity of the first-in-class agent bortezomib. Recently, the second-generation proteasome inhibitor carfilzomib has been approved in the USA in the relapsed and refractory setting, and several other investigational agents are in clinical development, including MLN9708, marizomib, oprozomib and delanzomib. Here, the authors provide a comprehensive review of the key role of proteasome inhibitors in the myeloma treatment pathway, and highlight the similarities and differences in pharmacology, routes of administration, and efficacy and safety profiles between bortezomib, carfilzomib and investigational agents. The authors also evaluate the potential for further improving myeloma treatment through the ongoing development of novel proteasome inhibitors.
蛋白酶体抑制已被证明是治疗多发性骨髓瘤的有效策略,这一点已被首个蛋白酶体抑制剂硼替佐米的临床活性所证实。最近,第二代蛋白酶体抑制剂卡非佐米已在美国复发性和难治性环境中获得批准,还有其他几种在研药物正在临床开发中,包括 MLN9708、马利佐米、奥普佐米和丹那佐米。在这里,作者全面回顾了蛋白酶体抑制剂在骨髓瘤治疗途径中的关键作用,并强调了硼替佐米、卡非佐米和在研药物在药理学、给药途径以及疗效和安全性特征方面的异同。作者还评估了通过正在开发的新型蛋白酶体抑制剂进一步改善骨髓瘤治疗的潜力。