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外周 T 细胞淋巴瘤中的表观遗传学异常和靶点。

Epigenetic Aberrations and Targets in Peripheral T-Cell Lymphoma.

机构信息

Division of Hematology and Medical Oncology, Melvin and Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN.

Lymphoma Program, Division of Hematology and Medical Oncology, Melvin and Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN.

出版信息

Clin Lymphoma Myeloma Leuk. 2022 Sep;22(9):659-665. doi: 10.1016/j.clml.2022.04.015. Epub 2022 Apr 22.

Abstract

Peripheral T cell lymphomas (PTCL) comprise a diverse group of aggressive T-cell and NK-cell lymphomas with many subtypes sharing same treatment algorithms despite having different pathobiology and responses to treatment. The molecular advances made in discovery of genetic mutations that disrupt epigenetic modulation in some subtypes of PTCL such as angioimmunoblastic T cell lymphoma and PTCL-not otherwise specified (NOS) may explain the poor outcomes and unsatisfactory responses to frontline line CHOP and CHOP-like therapy seen in this group of lymphomas. In this article, we address the main genetic mutations such as IDH2, TET2 and DNMT3A seen in PTCL and that disrupt the epigenetic modulation pathways, focusing on acetylation, deacetylation and methylation. Since therapeutic agents that target the disrupted epigenetic modulation pathways in PTCL may change treatment landscape in the near future, we will highlight the ones approved for treatment of refractory and/or relapsed PTCL and also the pivotal regimens being evaluated in clinical trials for treatment of frontline and refractory relapsed disease. We stress the importance of determining whether there is an association between the discussed genetic mutations and responses to the highlighted therapeutic agents such that treatments could be better tailored in patients with this kind of lymphoma with unmet needs.

摘要

外周 T 细胞淋巴瘤(PTCL)包括一组具有侵袭性的 T 细胞和 NK 细胞淋巴瘤,尽管具有不同的病理生物学和对治疗的反应,但许多亚型都有相同的治疗方案。在发现某些 PTCL 亚型(如血管免疫母细胞性 T 细胞淋巴瘤和未特指的 PTCL[NOS])中破坏表观遗传调节的遗传突变方面取得的分子进展,可能可以解释在这组淋巴瘤中看到的不良结局和对一线 CHOP 和 CHOP 样治疗的不满意反应。在本文中,我们将重点介绍 IDH2、TET2 和 DNMT3A 等在外周 T 细胞淋巴瘤中发现的主要基因突变,这些突变破坏了表观遗传调节途径,重点是乙酰化、去乙酰化和甲基化。由于针对 PTCL 中破坏的表观遗传调节途径的治疗药物可能会在不久的将来改变治疗格局,我们将重点介绍那些已被批准用于治疗难治性和/或复发性 PTCL 的药物,以及正在临床试验中评估的用于治疗一线和难治性复发疾病的关键方案。我们强调了确定所讨论的遗传突变与突出治疗药物反应之间是否存在关联的重要性,以便能够更好地为有这种未满足需求的淋巴瘤患者量身定制治疗方案。

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