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霍奇金淋巴瘤中的基因损伤与靶向治疗

Genetic lesions and targeted therapy in Hodgkin lymphoma.

作者信息

Li Zhe, Mu Wei, Xiao Min

机构信息

Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Hankou, Wuhan 430030, China.

出版信息

Ther Adv Hematol. 2023 Jan 12;14:20406207221149245. doi: 10.1177/20406207221149245. eCollection 2023.

Abstract

Hodgkin lymphoma is a special type of lymphoma in which tumor cells frequently undergo multiple genetic lesions that are associated with accompanying pathway abnormalities. These pathway abnormalities are dominated by active signaling pathways, such as the JAK-STAT (Janus kinase-signal transducer and activator of transcription) pathway and the NFκB (nuclear factor kappa-B) pathway, which usually result in hyperactive survival signaling. Targeted therapies often play an important role in hematologic malignancies, such as CAR-T therapy (chimeric antigen receptor T-cell immunotherapy) targeting CD19 and CD22 in diffuse large B-cell lymphoma, while in Hodgkin lymphoma, the main targets of targeted therapies are CD30 molecules and PD1 molecules. Drugs targeting other molecules are also under investigation. This review summarizes the actionable genetic lesions, current treatment options, clinical trials for Hodgkin lymphoma and the potential value of those genetic lesions in clinical applications.

摘要

霍奇金淋巴瘤是一种特殊类型的淋巴瘤,其中肿瘤细胞经常发生多种与伴随的信号通路异常相关的基因损伤。这些信号通路异常以活跃的信号通路为主导,如JAK-STAT(Janus激酶-信号转导和转录激活因子)通路和NFκB(核因子κB)通路,它们通常导致生存信号过度活跃。靶向治疗在血液系统恶性肿瘤中往往发挥重要作用,例如在弥漫性大B细胞淋巴瘤中靶向CD19和CD22的CAR-T疗法(嵌合抗原受体T细胞免疫疗法),而在霍奇金淋巴瘤中,靶向治疗的主要靶点是CD30分子和PD1分子。针对其他分子的药物也在研究中。本文综述了霍奇金淋巴瘤可操作的基因损伤、当前的治疗选择、临床试验以及这些基因损伤在临床应用中的潜在价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea6f/9841868/2b1d4320d330/10.1177_20406207221149245-fig1.jpg

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