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T细胞非霍奇金淋巴瘤的当前免疫治疗方法

Current Immunotherapeutic Approaches in T Cell Non-Hodgkin Lymphomas.

作者信息

Poggio Teresa, Duyster Justus, Illert Anna L

机构信息

Department of Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.

Faculty of Biology, Albert Ludwigs University of Freiburg, 79104 Freiburg, Germany.

出版信息

Cancers (Basel). 2018 Sep 18;10(9):339. doi: 10.3390/cancers10090339.

DOI:10.3390/cancers10090339
PMID:30231561
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6162531/
Abstract

T cell non-Hodgkin lymphoma (T-NHL) is a rare and heterogeneous group of neoplasms of the lymphoid system. With the exception of a few relatively indolent entities, T-NHL is typically aggressive, treatment resistant, and associated with poor prognosis. Relatively few options with proven clinical benefit are available for patients with relapsed or refractory disease. Immunotherapy has emerged as a promising treatment for the management of patients with hematological malignancies. The identification of tumor antigens has provided a large number of potential targets. Therefore, several monoclonal antibodies (alemtuzumab, SGN-30, brentuximab vedotin, and mogamulizumab), directed against tumor antigens, have been investigated in different subtypes of T-NHL. In addition to targeting antigens involved in cancer cell physiology, antibodies can stimulate immune effector functions or counteract immunosuppressive mechanisms. Chimeric antigen receptor (CAR)-T cells directed against CD30 and immune checkpoint inhibitors are currently being investigated in clinical trials. In this review, we summarize the currently available clinical evidence for immunotherapy in T-NHL, focusing on the results of clinical trials using first generation monoclonal antibodies, new immunotherapeutic agents, immune checkpoint inhibitors, and CAR-T cell therapies.

摘要

T细胞非霍奇金淋巴瘤(T-NHL)是一组罕见且异质性的淋巴系统肿瘤。除了少数相对惰性的实体瘤外,T-NHL通常具有侵袭性、耐药性,且预后较差。对于复发或难治性疾病患者,具有已证实临床益处的治疗选择相对较少。免疫疗法已成为治疗血液系统恶性肿瘤患者的一种有前景的治疗方法。肿瘤抗原的鉴定提供了大量潜在靶点。因此,几种针对肿瘤抗原的单克隆抗体(阿仑单抗、SGN-30、本妥昔单抗和莫加莫拉单抗)已在T-NHL的不同亚型中进行了研究。除了靶向参与癌细胞生理过程的抗原外,抗体还可以刺激免疫效应功能或对抗免疫抑制机制。目前,针对CD30的嵌合抗原受体(CAR)-T细胞和免疫检查点抑制剂正在临床试验中进行研究。在本综述中,我们总结了目前T-NHL免疫疗法的临床证据,重点关注使用第一代单克隆抗体、新型免疫治疗药物、免疫检查点抑制剂和CAR-T细胞疗法的临床试验结果。

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