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原发性中枢神经系统淋巴瘤新型治疗药物进展

英文原题:Update on Novel Therapeutics for Primary CNS Lymphoma.

查看英文原题

Update on Novel Therapeutics for Primary CNS Lymphoma.

PubMed 2021/10/26(内容时间) Cancers (Basel) Q2 · IF 4.8(JCR 2025)

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中文摘要

原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见淋巴瘤,局限于中枢神经系统或玻璃体视网膜区域。标准治疗为甲氨蝶呤为基础的细胞毒性化疗,可联合或不联合放疗。尽管缓解率较高,复发仍很常见,凸显开发新疗法的必要性。近期对PCNSL认识的进展揭示了其发病和耐药机制,包括B细胞受体和哺乳动物雷帕霉素靶蛋白通路活化。新型治疗策略,如布鲁顿酪氨酸激酶(BTK)抑制剂伊布替尼、磷脂酰肌醇3激酶(PI3K)抑制剂及免疫调节药物,均显示出前景。越来越多证据表明,免疫逃逸参与PCNSL发病过程;目前正在研究多种免疫疗法,包括免疫检查点抑制和靶向性CAR-T(CAR-T)细胞。本综述讨论靶向治疗策略开发中的挑战,更新近期治疗进展,并展望正在进行的临床研究。

展开英文摘要原文

Primary central nervous system lymphoma (PCNSL) is a rare lymphoma isolated to the central nervous system or vitreoretinal space. Standard treatment consists of cytotoxic methotrexate-based chemotherapy, with or without radiation. Despite high rates of response, relapse is common, highlighting the need for novel therapeutic approaches. Recent advances in the understanding of PCNSL have elucidated mechanisms of pathogenesis and resistance including activation of the B-cell receptor and mammalian target of rapamycin pathways.

Novel treatment strategies such as the Bruton's tyrosine kinase (BTK) inhibitor ibrutinib, phosphatidylinositol-3 kinase (PI3K) inhibitors, and immunomodulatory drugs are promising. Increasingly, evidence suggests immune evasion plays a role in PCNSL pathogenesis and several immunotherapeutic strategies including checkpoint inhibition and targeted chimeric antigen receptor T (CAR-T) cells are under investigation.

This review provides a discussion on the challenges in development of targeted therapeutic strategies, an update on recent treatment advances, and offers a look toward ongoing clinical studies.

论文信息

作者
Schaff LR、Grommes C
单位
Memorial Sloan Kettering Cancer Center, Department of Neurology, Weill Cornell Medicine, New York, NY 10065, USA.United States
文献类型
综述
期刊
Cancers2021 Oct 26
原文标识
PubMed 34771535 · DOI 10.3390/cancers13215372