Ahmed Nada, Feldman Andrew L
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Expert Rev Hematol. 2020 Feb;13(2):127-139. doi: 10.1080/17474086.2020.1711732. Epub 2020 Jan 22.
: T-cell lymphomas represent a broad group of malignant T-cell neoplasms with marked molecular, clinical, and biologic heterogeneity. Survival rates after conventional chemotherapy regimens are poor for most subtypes and new therapies are needed. Rapidly expanding knowledge in the field of epigenomics and the development of an increasing number of epigenetic-modifying agents have created new opportunities for epigenetic therapies for patients with this complex group of diseases.: The present review summarizes current knowledge on epigenetic alterations in T-cell lymphomas, availability, and mechanisms of action of epigenetic-modifying agents, results of clinical trials of epigenetic therapies in T-cell lymphomas, status of FDA approval, and biomarker approaches to guide therapy. Promising future directions are discussed.: Mutations in epigenetic-modifying genes are among the most common genetic alterations in T-cell lymphomas, highlighting the potential for epigenetic therapies to improve management of this group of diseases. Single-agent efficacy is well documented, leading to FDA approval for several indications, but overall response rates and durability of responses remain modest. Critical next steps for the field include optimizing combination therapies that incorporate epigenetic-modifying agents and developing predictive biomarkers that help guide patient and drug selection.
T细胞淋巴瘤是一大类恶性T细胞肿瘤,具有显著的分子、临床和生物学异质性。对于大多数亚型而言,传统化疗方案后的生存率很低,因此需要新的治疗方法。表观基因组学领域知识的迅速扩展以及越来越多表观遗传修饰剂的开发,为患有这类复杂疾病的患者带来了表观遗传治疗的新机遇。
本综述总结了目前关于T细胞淋巴瘤表观遗传改变的知识、表观遗传修饰剂的可用性和作用机制、T细胞淋巴瘤表观遗传治疗的临床试验结果、美国食品药品监督管理局(FDA)的批准情况以及指导治疗的生物标志物方法。还讨论了有前景的未来方向。
表观遗传修饰基因的突变是T细胞淋巴瘤中最常见的基因改变之一,这凸显了表观遗传治疗改善这类疾病管理的潜力。单药疗效已有充分记录,促使FDA批准了多项适应症,但总体缓解率和缓解持续时间仍然有限。该领域接下来的关键步骤包括优化包含表观遗传修饰剂的联合治疗方案,以及开发有助于指导患者和药物选择的预测性生物标志物。