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使用布鲁顿酪氨酸激酶(BTK)抑制剂联合利妥昔单抗及大剂量甲氨蝶呤成功治疗合并中枢神经系统受累的噬血细胞性血管内大B细胞淋巴瘤。

Successful treatment of hemophagocytic intravascular large B-cell lymphoma with CNS involvement with BTK inhibitor combined with rituximab and high-dose methotrexate.

作者信息

Shao Fangfei, Su Wei, Zhao Xiujie, He Jianping, Wang Xiaofen, Guo Feng, Xiao Haowen

机构信息

Department of Hematology and Cell Therapy, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, P.R. China.

Department of Hematology and Cell Therapy, Shaoxing Shangyu Hospital of Traditional Chinese Medicine, Sir Run Run Shaw Hospital Shaoxing Branch, Zhejiang University School of Medicine, Hangzhou, Zhejiang, P.R. China.

出版信息

Ther Adv Hematol. 2024 Aug 15;15:20406207241270788. doi: 10.1177/20406207241270788. eCollection 2024.

Abstract

This is a case of hemophagocytic intravascular large B-cell lymphoma (IVLBCL) with central nervous system (CNS) involvement. Although R-CHOP chemotherapy regimen has been shown significant improvement in survival rate. The prognosis and outcomes remain unsatisfactory, which is identified as outstanding challenges and need solutions. Gene and molecular profiling studies may provide new therapeutic strategies, especially the BCR/TLR/IL-1R/NF-κB signaling pathway in IVLBCL. Here, we treated the hemophagocytic IVLBCL CNS-involved patient with the Bruton tyrosine kinase inhibitor (BTKi) to block NF-κB pathway, and indicated that the second-generation BTKi zanubrutinib-based treatment was feasible and efficient.

摘要

这是一例伴有中枢神经系统(CNS)受累的噬血细胞性血管内大B细胞淋巴瘤(IVLBCL)。尽管R-CHOP化疗方案已显示出存活率有显著提高。但其预后和结果仍不尽人意,这被视为突出的挑战且需要解决办法。基因和分子谱研究可能会提供新的治疗策略,特别是针对IVLBCL中的BCR/TLR/IL-1R/NF-κB信号通路。在此,我们使用布鲁顿酪氨酸激酶抑制剂(BTKi)治疗噬血细胞性IVLBCL累及CNS的患者以阻断NF-κB通路,并表明基于第二代BTKi泽布替尼的治疗是可行且有效的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b2/11325336/e02f2cc75019/10.1177_20406207241270788-fig1.jpg

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