SOHO State of the Art Updates and Next Questions | New Pathways and New Targets in PTCL: Staying on Target

被引:2
|
作者
Carty, Shannon A. [1 ]
Murga-Zamalloa, Carlos A. [2 ]
Wilcox, Ryan A. [1 ,3 ]
机构
[1] Univ Michigan, Dept Internal Med, Div Hematol & Oncol, Ann Arbor, MI USA
[2] Univ Illinois, Dept Pathol, Chicago, IL USA
[3] Univ Michigan, Rogel Canc Ctr, Dept Internal Med, Div Hematol & Oncol, Canc Ctr 4310,1500 East Med Ctr Dr, Ann Arbor, MI 48109 USA
来源
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA | 2023年 / 23卷 / 08期
关键词
Peripheral T-cell lymphoma; T-cell receptor; JAK; Macrophage; Tumor microenvironment; T-CELL LYMPHOMA; TYROSINE KINASE INHIBITOR; FOLLICULAR HELPER; ENHANCER LANDSCAPE; MYCOSIS-FUNGOIDES; ACTIVATING MUTATIONS; CD28; COSTIMULATION; GENOMIC ANALYSIS; SEZARY-SYNDROME; FUSION KINASE;
D O I
10.1016/j.clml.2023.04.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
While the peripheral T-cell lymphomas (PTCL) remain a therapeutic challenge, and increasingly account for a disproportionate number of lymphoma-related deaths, improved understanding of disease pathogenesis and classification, and the development of novel therapeutic agents over the past decade, all provide reasons for a more optimistic outlook in the next. Despite their genetic and molecular heterogeneity, many PTCL are dependent upon signaling input provided by antigen, costimulatory, and cytokine receptors. While gain-of-function alterations effecting these pathways are recurrently observed in many PTCL, more often than not, signaling remains ligand-and tumor microenvironment (TME)- dependent. Consequently, the TME and its constituents are increasingly recognized as "on target". Utilizing a "3 signal" model, we will review new-and old-therapeutic targets that are relevant for the more common nodal PTCL subtypes.
引用
收藏
页码:561 / 574
页数:14
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