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EB 病毒阳性弥漫大 B 细胞淋巴瘤(NOS)的生物学与治疗

英文原题:The biology and treatment of Epstein-Barr virus-positive diffuse large B cell lymphoma, NOS.

查看英文原题

The biology and treatment of Epstein-Barr virus-positive diffuse large B cell lymphoma, NOS.

PubMed 2023/12/27(内容时间) Heliyon

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中文摘要

EBV阳性弥漫大B细胞淋巴瘤,非特指型(EBV+DLBCL-NOS)是指肿瘤细胞核中表达EBV编码RNA的DLBCL。EBV+DLBCL-NOS患者就诊时临床分期更晚,结外受累更常见。尽管含利妥昔单抗的免疫化疗方案可显著改善EBV+DLBCL患者的预后,但最佳一线治疗仍需进一步探索。由于EBV+DLBCL-NOS发病率相对较低且存在地区差异,关于这一特殊淋巴瘤亚型的认识仍然有限。EBV+DLBCL-NOS中一些信号通路异常激活,包括NF-κB和JAK/STAT通路及其他信号转导通路。此外,还观察到干扰素反应、抗原呈递系统和免疫检查点分子异常等免疫过程。目前,CAR-T 细胞治疗、化疗联合免疫治疗及新型靶向治疗药物有望改善EBV+DLBCL-NOS患者的预后,但仍需更多研究加以证实。

展开英文摘要原文

EBV positive Diffuse Large B-cell lymphoma, not otherwise specified (EBV+DLBCL-NOS) referred to DLBCL with expression of EBV encoded RNA in tumor nucleus. EBV+DLBCL-NOS patients present with more advanced clinical stages and frequent extranodal involvement. Although rituximab-containing immunochemotherapy regimens can significantly improve outcomes in patients with EBV+DLBCL, the best first-line treatment needs to be further explored.

Due to the relatively low incidence and regional variation of EBV+DLBCL-NOS, knowledge about this particular subtype of lymphoma remains limited. Some signaling pathways was abnormally activated in EBV+DLBCL-NOS, including NF- B and JAK/STAT pathways) and other signal transduction pathways.

In addition, immune processes such as interferon response, antigen-presenting system and immune checkpoint molecule abnormalities were also observed. Currently, chimeric antigen receptor T-cell (CAR-T) therapy, chemotherapy combined with immunotherapy and novel targeted therapeutic drugs are expected to improve the prognosis of EBV+DLBCL-NOS patients, but more studies are needed to confirm this.

论文信息

作者
Li JW、Deng C、Zhou XY、Deng R
第一作者单位
Department of Oncology, The Second Xiangya Hospital, Central South University, Changsha, 410000, China.China
通讯作者单位
Department of Oncology, The Second Hospital of Zhuzhou City, Zhuzhou, 412000, China.China
文献类型
综述
期刊
Heliyon2024 Jan 15
原文标识
PubMed 38234917 · DOI 10.1016/j.heliyon.2023.e23921