Suppr超能文献

奥雷巴替尼联合利妥昔单抗及大剂量甲氨蝶呤治疗原发性或继发性中枢神经系统弥漫性大B细胞淋巴瘤的疗效及安全性:一项回顾性分析

Efficacy and safety of orelabrutinib combined with rituximab and high dose methotrexate in primary or secondary central nervous system diffuse large B-cell lymphoma: a retrospective analysis.

作者信息

Zhou Jiahao, Xing Lingxiao, Miao Yi, Qin Shuchao, Zhang Run, Tang Hanning, Xu Wei, Xia Yi, Zhu Huayuan, Li Jianyong

机构信息

Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing, 210029, Jiangsu, China.

Key Laboratory of Hematology of Nanjing Medical University, Nanjing, 210029, Jiangsu, China.

出版信息

Invest New Drugs. 2025 May 31. doi: 10.1007/s10637-025-01542-7.

Abstract

Central nervous system lymphoma (CNSL) are mainly diffuse large B-cell lymphomas (DLBCLs). Orelabrutinib is a second-generation Bruton's tyrosine kinase (BTK) inhibitor and has shown single-agent activity in CNSL. This study aims to evaluate the efficacy and safety of orelabrutinib combined with rituximab and high dose methotrexate (ORM) regimen in the treatment of patients with CNSL. We retrospectively analyzed data from CNSL patients treated with ORM regimen at Jiangsu Province Hospital, the First Affiliated Hospital of Nanjing Medical University from April 2021 to October 2023. Patients receiving rituximab plus high-dose methotrexate (RM regimen) from June 2017 to January 2024 were identified as the control group. Progression-free survival (PFS) and overall survival (OS) were estimated using the Kaplan-Meier method. Adverse events (AEs) were assessed according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. A total of 32 patients were identified: 14 patients in the ORM group and 18 in the RM group. CR rates were 84.6% in the ORM group and 44.4% in the RM group (P = 0.032). Median PFS was 18.6 months in the RM group and 26.3 months in the ORM group (P = 0.133). Median OS was 34.1 months in the RM group and has not yet been reached in the ORM group (P = 0.041). Patients in the ORM group showed a higher 2-year OS rate than those in the RM group (82.1% vs. 57.5%). No grade 5 AE was reported in both groups. The incidence of grade 3-4 AE was comparable between the two treatment groups. ORM regimen was effective and well-tolerated in patients with CNSL. This combination therapy provides a new potential therapeutic strategy for patients with CNSL.

摘要

中枢神经系统淋巴瘤(CNSL)主要为弥漫性大B细胞淋巴瘤(DLBCL)。奥雷巴替尼是第二代布鲁顿酪氨酸激酶(BTK)抑制剂,已显示出对CNSL的单药活性。本研究旨在评估奥雷巴替尼联合利妥昔单抗及大剂量甲氨蝶呤(ORM)方案治疗CNSL患者的疗效和安全性。我们回顾性分析了2021年4月至2023年10月在南京医科大学第一附属医院江苏省人民医院接受ORM方案治疗的CNSL患者的数据。将2017年6月至2024年1月接受利妥昔单抗加大剂量甲氨蝶呤(RM方案)治疗的患者确定为对照组。采用Kaplan-Meier法估计无进展生存期(PFS)和总生存期(OS)。根据不良事件通用术语标准(CTCAE)第5.0版评估不良事件(AE)。共纳入32例患者:ORM组14例,RM组18例。ORM组的完全缓解(CR)率为84.6%,RM组为44.4%(P = 0.032)。RM组的中位PFS为18.6个月,ORM组为

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验