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血液系统恶性肿瘤中的蛋白酶体抑制作用。

Proteasome inhibition in hematologic malignancies.

作者信息

Richardson Paul G, Hideshima Teru, Mitsiades Constantine, Anderson Kenneth

机构信息

Dana-Farber Cancer, Institute, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Ann Med. 2004;36(4):304-14. doi: 10.1080/07853890410030877.

Abstract

Hematologic malignancies, including multiple myeloma (MM), will account for more than 100,000 new cases of cancer and over 57,000 deaths in the United States in 2003. Treatment of MM is a serious challenge, because despite a variety of available therapies, median survival is short. A new therapeutic area focuses on inhibiting the activity of the proteasome, a 26S protease complex involved in cell cycle regulation, cell adhesion, inflammation, and protein turnover. The novel proteasome inhibitor, bortezomib (Velcade), was recently approved for use in patients with refractory and relapsed MM and to date is the only proteasome inhibitor to have entered clinical trials. Bortezomib has demonstrated activity with manageable toxicity in a variety of hematologic malignancies in addition to MM, including leukemia and non-Hodgkin's lymphoma. This article reviews clinical information on bortezomib in hematologic malignancies both as monotherapy and in combination with dexamethasone. Preliminary reports of bortezomib in combination with Doxil (pegylated liposomal doxorubicin), melphalan, and thalidomide are discussed, and current trials are described. Available data suggest that bortezomib will be useful in the treatment of a variety of hematologic malignancies.

摘要

2003年,包括多发性骨髓瘤(MM)在内的血液系统恶性肿瘤在美国将导致超过10万例新发癌症病例和超过5.7万例死亡。多发性骨髓瘤的治疗是一项严峻挑战,因为尽管有多种可用疗法,但中位生存期较短。一个新的治疗领域聚焦于抑制蛋白酶体的活性,蛋白酶体是一种参与细胞周期调控、细胞黏附、炎症和蛋白质周转的26S蛋白酶复合体。新型蛋白酶体抑制剂硼替佐米(万珂)最近被批准用于难治性和复发性多发性骨髓瘤患者,并且是迄今为止唯一进入临床试验的蛋白酶体抑制剂。除多发性骨髓瘤外,硼替佐米在包括白血病和非霍奇金淋巴瘤在内的多种血液系统恶性肿瘤中已显示出活性且毒性可控。本文综述了硼替佐米在血液系统恶性肿瘤中作为单一疗法以及与地塞米松联合使用的临床信息。讨论了硼替佐米与多柔比星脂质体(聚乙二醇化脂质体阿霉素)、美法仑和沙利度胺联合使用的初步报告,并描述了当前的试验。现有数据表明硼替佐米将有助于治疗多种血液系统恶性肿瘤。

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