Peripheral T-cell lymphoma

Author:

Foss Francine M.1,Zinzani Pier Luigi2,Vose Julie M.3,Gascoyne Randy D.4,Rosen Steven T.5,Tobinai Kensei6

Affiliation:

1. Yale Cancer Center, New Haven, CT;

2. Institute of Hematology and Medical Oncology Seràgnoli, University of Bologna, Bologna, Italy;

3. University of Nebraska Medical Center, Omaha, NE;

4. British Columbia Cancer Agency, Vancouver, BC;

5. Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Feinberg School of Medicine, Chicago, IL; and

6. National Cancer Center Hospital, Tokyo, Japan

Abstract

AbstractPeripheral 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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