Peripheral T-cell lymphoma

被引:226
作者
Foss, Francine M. [1 ]
Zinzani, Pier Luigi [2 ]
Vose, Julie M. [3 ]
Gascoyne, Randy D. [4 ]
Rosen, Steven T. [5 ]
Tobinai, Kensei [6 ]
机构
[1] Yale Canc Ctr, New Haven, CT 06520 USA
[2] Univ Bologna, Inst Hematol & Med Oncol Seragnoli, Bologna, Italy
[3] Univ Nebraska Med Ctr, Omaha, NE USA
[4] British Columbia Canc Agcy, Vancouver, BC V5Z 4E6, Canada
[5] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Feinberg Sch Med, Chicago, IL 60611 USA
[6] Natl Canc Ctr, Tokyo, Japan
关键词
GENE-EXPRESSION ANALYSIS; EPSTEIN-BARR-VIRUS; 3-WEEKLY CHOP CHEMOTHERAPY; HIGH-DOSE CHEMOTHERAPY; PHASE-II TRIAL; LEUKEMIA-LYMPHOMA; PROGNOSTIC-SIGNIFICANCE; AGGRESSIVE LYMPHOMAS; COMPLETE REMISSION; HODGKINS-LYMPHOMA;
D O I
10.1182/blood-2010-05-231548
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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, his-tone 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. (Blood. 2011;117(25):6756-6767)
引用
收藏
页码:6756 / 6767
页数:12
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