Advances in the understanding and treatment of Cutaneous T-cell Lymphoma

被引:5
作者
Bakr, Farrah S. [1 ]
Whittaker, Sean J. [1 ]
机构
[1] Kings Coll London, St Johns Inst Dermatol, Sch Basic & Biomed Sci, London, England
关键词
cutaneous T cell lymphoma (CTCL); dermatology; pathway targeted interventions; genomics; cutaneous lymphoma; SEZARY-SYNDROME; MYCOSIS-FUNGOIDES; ATAXIA-TELANGIECTASIA; MUTATIONAL LANDSCAPE; GERMLINE MUTATIONS; DNA METHYLATION; ATM GENE; KINASE; TRIAL; MULTICENTER;
D O I
10.3389/fonc.2022.1043254
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cutaneous T-cell lymphomas (CTCL) are a heterogeneous group of non-Hodgkin's lymphomas (NHL) characterised by the clonal proliferation of malignant, skin homing T-cells. Recent advances have been made in understanding the molecular pathogenesis of CTCL. Multiple deep sequencing studies have revealed a complex genomic landscape with large numbers of novel single nucleotide variants (SNVs) and copy number variations (CNVs). Commonly perturbed genes include those involved in T-cell receptor signalling, T-cell proliferation, differentiation and survival, epigenetic regulators as well as genes involved in genome maintenance and DNA repair. In addition, studies in CTCL have identified a dominant UV mutational signature in contrast to systemic T-cell lymphomas and this likely contributes to the high tumour mutational burden. As current treatment options for advanced stages of CTCL are associated with short-lived responses, targeting these deregulated pathways could provide novel therapeutic approaches for patients. In this review article we summarise the key pathways disrupted in CTCL and discuss the potential therapeutic implications of these findings.
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页数:10
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