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硼替佐米用于套细胞淋巴瘤的治疗。

Bortezomib in mantle cell lymphoma.

作者信息

Suh K Stephen, Goy Andre

机构信息

Jurist Research Center, 30 Prospect Avenue, Hackensack NJ 07601, USA.

出版信息

Future Oncol. 2008 Apr;4(2):149-68. doi: 10.2217/14796694.4.2.149.

Abstract

Mantle cell lymphoma (MCL) represents 6% of non-Hodgkin lymphomas, but is one of the most active fields of clinical investigation. Unfortunately, there is still no standard or curative therapy in MCL. Front-line therapy appears to benefit from intensification either through high-dose therapy with stem cell transplant consolidation or dose-intense chemotherapy with hyperfractionated cyclophosphamide, vincristine, adriamycin/doxorubicin and dexamethasone/rituximab. Most patients still relapse and a multitude of novel agents are currently being tested in this setting, including proteasome inhibitors with bortezomib (the first of its class and the first US FDA-approved drug for MCL), mTOR inhibitors, Bcl-2 inhibitors, antiangiogenesis agents and histone deacetylase inhibitors among others. An obvious effort is needed to enroll patients on clinical trials, the design of which might benefit from pharmacogenomics and a better understanding of MCL biology and its diversity.

摘要

套细胞淋巴瘤(MCL)占非霍奇金淋巴瘤的6%,却是临床研究最活跃的领域之一。不幸的是,MCL仍没有标准或治愈性疗法。一线治疗似乎可通过干细胞移植巩固的大剂量疗法或含超分割环磷酰胺、长春新碱、阿霉素/多柔比星及地塞米松/利妥昔单抗的剂量密集化疗得到强化。大多数患者仍会复发,目前在此背景下正在测试多种新型药物,包括蛋白酶体抑制剂硼替佐米(该类中的首个药物及首个获美国食品药品监督管理局批准用于MCL的药物)、mTOR抑制剂、Bcl-2抑制剂、抗血管生成药物及组蛋白去乙酰化酶抑制剂等。需要做出明显努力让患者参加临床试验,其设计可能受益于药物基因组学以及对MCL生物学及其多样性的更好理解。

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