Yale Cancer Center, New Haven, CT, USA.
Blood. 2011 Jun 23;117(25):6756-67. doi: 10.1182/blood-2010-05-231548. Epub 2011 Apr 14.
Peripheral T-cell lymphomas (PTCLs) are a heterogeneous group of clinically aggressive diseases associated with poor outcome. Studies that focus specifically on PTCL are emerging, with the ultimate goal of improved understanding of disease biology and the development of more effective therapies. However, one of the difficulties in classifying and studying treatment options in clinical trials is the rarity of these subtypes. Various groups have developed lymphoma classifications over the years, including the World Health Organization, which updated its classification in 2008. This article briefly reviews the major lymphoma classification schema, highlights contributions made by the collaborative International PTCL Project, discusses prognostic issues and gene expression profiling, and outlines therapeutic approaches to PTCL. These include the standard chemotherapeutic regimens and other modalities incorporating antifolates, conjugates, histone deacetylase inhibitors, monoclonal antibodies, nucleoside analogs, proteasome inhibitors, and signaling inhibitors. As this review emphasizes, the problem has now evolved into an abundance of drugs and too few patients available to test them. Collaborative groups will aid in future efforts to find the best treatment strategies to improve the outcome for patients with PTCL.
外周 T 细胞淋巴瘤(PTCL)是一组具有临床侵袭性、预后不良的异质性疾病。目前,越来越多的研究专门针对 PTCL,以期深入了解疾病生物学,并开发更有效的治疗方法。然而,在临床试验中对这些亚型进行分类和研究治疗方案存在一个困难,那就是这些亚型较为罕见。多年来,各种组织已经制定了淋巴瘤分类,包括世界卫生组织(WHO),其在 2008 年更新了分类。本文简要回顾了主要的淋巴瘤分类方案,重点介绍了国际 PTCL 项目合作组织的贡献,讨论了预后问题和基因表达谱分析,并概述了 PTCL 的治疗方法。这些方法包括标准化疗方案和其他包含叶酸类似物、偶联物、组蛋白去乙酰化酶抑制剂、单克隆抗体、核苷类似物、蛋白酶体抑制剂和信号抑制剂的治疗方式。正如本文所强调的,现在的问题已经演变成药物过多而可供测试的患者太少。合作团体将有助于未来寻找最佳治疗策略,以改善 PTCL 患者的预后。