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原发性中枢神经系统淋巴瘤的新型药物治疗:现状与展望。

Novel agents for primary central nervous system lymphoma: evidence and perspectives.

机构信息

Department of Hematology/Oncology and Palliative Care, Klinikum Stuttgart, Stuttgart, Germany.

Department of Hematology, Oncology and Stem Cell Transplantation, Faculty of Medicine, University of Freiburg, Freiburg, Germany; and.

出版信息

Blood. 2018 Aug 16;132(7):681-688. doi: 10.1182/blood-2018-01-791558. Epub 2018 Jul 9.

DOI:10.1182/blood-2018-01-791558
PMID:29986908
Abstract

Primary central nervous system lymphoma (PCNSL) is a rare aggressive extranodal non- Hodgkin lymphoma. Although high remission rates can be achieved with high-dose methotrexate-based immunochemotherapy, risk of relapse and associated death is still substantial in at least a third of patients. Novel agents for treating lymphoid malignancies have substantially enriched treatment options for PCNSL. We herein systematically review the existing clinical evidence of novel agents in treatment of PCNSL, summarize ongoing studies, and discuss perspectives. The body of evidence for novel agents is still limited to noncomparative studies, but the most promising approaches include Bruton kinase inhibition with ibrutinib and immunomodulatory treatment (eg, with lenalidomide). Targeting the mammalian target of rapamycin pathway does not seem to have a meaningful clinical benefit, and evidence of checkpoint inhibition with nivolumab is limited to anecdotal evidence. Future studies should embrace the concept of induction and maintenance therapy as well as the combination of drugs with different mechanisms of action. Selection of patients based on molecular profiling and relapse patterns should be another aspect informing future comparative trials, which are urgently needed to improve prognosis for patients with PCNSL.

摘要

原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的侵袭性结外非霍奇金淋巴瘤。尽管大剂量甲氨蝶呤为基础的免疫化疗可以达到很高的缓解率,但至少有三分之一的患者仍存在复发和相关死亡的高风险。新型治疗淋巴恶性肿瘤的药物为 PCNSL 的治疗提供了更多选择。本文系统回顾了新型药物治疗 PCNSL 的现有临床证据,总结了正在进行的研究,并讨论了相关观点。新型药物的证据仍然仅限于非对照研究,但最有前途的方法包括布鲁顿酪氨酸激酶抑制剂伊布替尼和免疫调节治疗(如来那度胺)。靶向哺乳动物雷帕霉素靶蛋白(mTOR)途径似乎没有明显的临床获益,而纳武单抗的检查点抑制作用的证据仅限于一些实例报告。未来的研究应采用诱导和维持治疗的概念,以及不同作用机制药物的联合治疗。基于分子谱和复发模式选择患者应是另一个为未来的比较试验提供信息的方面,迫切需要这些试验来改善 PCNSL 患者的预后。

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