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套细胞淋巴瘤的靶向治疗现状。

Current status of targeted therapies for mantle cell lymphoma.

机构信息

Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI 53705, USA.

出版信息

Drugs. 2011 Dec 3;71(17):2307-26. doi: 10.2165/11594630-000000000-00000.

Abstract

Mantle cell lymphoma (MCL) is a type of non-Hodgkin's lymphoma (NHL) with treatment outcomes that have historically been poorer than those observed with other NHL subtypes. Patients typically present with advanced-stage disease and frequent extranodal involvement; the median age at diagnosis is >60 years. Recent improvements in progression-free and overall survival have been observed with more dose-intensive strategies, although at least half of patients diagnosed with MCL are not eligible for such treatment approaches based on age and co-morbidities. In addition, therapy options for relapsed MCL are limited. Only bortezomib is approved for treatment of relapsed MCL in the US. Development of targeted therapy approaches to minimize toxicities while preserving anti-neoplastic properties is of particular importance in MCL. Multiple ongoing studies are attempting to build on the known efficacy of bortezomib by evaluating combination regimens with other targeted agents or cytotoxic chemotherapy. The mammalian target of rapamycin (mTOR) inhibitor temsirolimus has known activity in MCL, making this an attractive class of agents for further investigation in combination regimens. Rituximab and other monoclonal antibodies are being evaluated for novel roles in MCL treatment, including as maintenance therapy. Other classes of drugs being investigated in MCL are immunomodulatory agents, inhibitors of the phosphoinositide 3-kinase/Akt and B-cell receptor signalling pathways, and inhibitors of bcl-2 and histone deacetylase. Although many of the agents appear to have modest single-agent activity, the favourable toxicity profile of many agents will make them best suited for incorporation into combination regimens.

摘要

套细胞淋巴瘤(MCL)是一种非霍奇金淋巴瘤(NHL),其治疗效果历来不如其他 NHL 亚型。患者通常表现为晚期疾病和频繁的结外累及;诊断时的中位年龄>60 岁。最近,由于采用了更密集的剂量治疗策略,无进展生存期和总生存期有所改善,尽管至少有一半的 MCL 患者由于年龄和合并症而不符合此类治疗方法。此外,MCL 患者缓解后的治疗选择有限。在美国,只有硼替佐米被批准用于治疗复发性 MCL。开发靶向治疗方法以最大限度地减少毒性,同时保留抗肿瘤特性,在 MCL 中尤为重要。多项正在进行的研究试图通过评估与其他靶向药物或细胞毒性化疗联合的方案,在硼替佐米已知疗效的基础上进一步探索。哺乳动物雷帕霉素靶蛋白(mTOR)抑制剂替西罗莫司在 MCL 中有已知的活性,这使得它成为联合方案中进一步研究的一个有吸引力的药物类别。利妥昔单抗和其他单克隆抗体正在评估在 MCL 治疗中的新作用,包括作为维持治疗。正在研究的其他 MCL 药物类别是免疫调节剂、磷酸肌醇 3-激酶/Akt 和 B 细胞受体信号通路抑制剂以及 bcl-2 和组蛋白去乙酰化酶抑制剂。尽管许多药物似乎具有适度的单药活性,但许多药物良好的毒性特征将使它们最适合纳入联合治疗方案。

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