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套细胞淋巴瘤的当前治疗策略和新型药物。

Current treatment strategy and new agents in mantle cell lymphoma.

机构信息

Department of Hematology and Oncology, Nagoya Daini Red Cross Hospital, 2-9 Myokencho, Showaku, Nagoya, Japan.

出版信息

Int J Hematol. 2010 Jul;92(1):25-32. doi: 10.1007/s12185-010-0607-8. Epub 2010 Jun 8.

Abstract

Mantle cell lymphoma (MCL) is a well-recognized lymphoma subtype that accounts for about 5% of all patients with non-Hodgkin lymphoma. The clinical course of MCL ranges from an indolent disease to a rapidly progressive malignancy, with a poor prognosis and a median overall survival (OS) of about 3-5 years reported in earlier data sets. Knowledge of its biology has increased in the last few years. Unfortunately, this progress has not yet brought any major improvements in therapeutic approaches, which still remain highly unsatisfactory. Recent improvement has been achieved by the successful introduction of monoclonal antibodies and dose-intensified approaches including autologous stem cell transplantation strategies. However, with the exception of allogeneic hematopoietic stem cell transplantation, current treatment approaches are non-curative, and the corresponding survival curves are characterized by a delayed but continuous decline and a median survival of 4-6 years. In recent years, new insights into the biology of MCL have been obtained which have provided the rationale for the development of novel therapeutic strategies. Emerging new drugs such as bendamustine, proteasome inhibitors, antibodies, mTOR inhibitors, and immunomodulatory drugs and others are based on the dysregulated control of cell cycle machinery and impaired apoptotic pathways. The efficacy of these agents as monotherapy was demonstrated to be comparable to conventional chemotherapy in relapsed MCL, and combination strategies are currently being investigated in clinical trials.

摘要

套细胞淋巴瘤(MCL)是一种公认的淋巴瘤亚型,约占所有非霍奇金淋巴瘤患者的 5%。MCL 的临床病程从惰性疾病到快速进展的恶性肿瘤不等,在早期数据集中报告的预后较差,中位总生存期(OS)约为 3-5 年。近年来,对其生物学的认识有所增加。不幸的是,这一进展尚未在治疗方法上带来任何重大改进,这些方法仍然极不理想。最近的进展是通过成功引入单克隆抗体和剂量强化方法(包括自体干细胞移植策略)实现的。然而,除了异基因造血干细胞移植外,目前的治疗方法无法治愈,相应的生存曲线以延迟但持续下降为特征,中位生存时间为 4-6 年。近年来,对 MCL 生物学的新认识为开发新的治疗策略提供了依据。新兴的新药,如苯达莫司汀、蛋白酶体抑制剂、抗体、mTOR 抑制剂、免疫调节剂等,都是基于细胞周期机制的失调控制和凋亡途径的受损。这些药物作为单一疗法的疗效与复发型 MCL 中的常规化疗相当,目前正在临床试验中研究联合策略。

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