Wu Yuchen, Sun Xuefei, Lv Liwei, Cui Qu, Qian Jun, Xing Ruixian, Bai Xueyan, Chen Yuedan, Liu Qing, Lai Wenyuan, Gao Chunji, Sun Shengjun, Ji Nan, Liu Yuanbo
Department of Hematology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Department of Hematology, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Front Neurol. 2025 Jun 5;16:1570224. doi: 10.3389/fneur.2025.1570224. eCollection 2025.
Relapsed or refractory central nervous system lymphoma (rrCNSL) lacks established preferred treatment and carries an inferior prognosis. Bruton's tyrosine kinase inhibitor (BTKi) showed promising effectiveness. Orelabrutinib is a second-generation BTKi with a high concentration in cerebrospinal fluid.
In this retrospective analysis, the outcomes of 37 relapsed or refractory central nervous system diffuse large B-cell lymphoma patients who received orelabrutinib, high-dose methotrexate, ifosfamide, etoposide, and dexamethasone (Ore-MIED) or orelabrutinib, high-dose methotrexate, temozolomide and dexamethasone (Ore-MTD) were evaluated.
Of the 37 patients included, 11 received Ore-MTD, and 26 received the Ore-MIED regimen. The overall response rate in our cohort was 89.2%, with complete remission achieved in 51.4% of patients and partial remission in 37.8% of patients. The median progression-free survival was observed to be 7.0 months. No statistically significant difference was found in the median progression-free survival between patients receiving different treatment regimens (5.0 months for Ore-MTD versus 13.0 months for Ore-MIED; = 0.29). Moreover, the median overall survival has not been reached in this cohort, indicating a promising outcome despite the aggressive nature of the disease.
Our study confirms the effectiveness and safety of Ore-MIED/Ore-MTD in rrCNSL patients, even in those with previous exposure to multiple lines of treatment.
复发或难治性中枢神经系统淋巴瘤(rrCNSL)缺乏既定的首选治疗方法,预后较差。布鲁顿酪氨酸激酶抑制剂(BTKi)显示出有前景的疗效。奥雷巴替尼是一种第二代BTKi,在脑脊液中浓度较高。
在这项回顾性分析中,评估了37例接受奥雷巴替尼、大剂量甲氨蝶呤、异环磷酰胺、依托泊苷和地塞米松(Ore-MIED)或奥雷巴替尼、大剂量甲氨蝶呤、替莫唑胺和地塞米松(Ore-MTD)治疗的复发或难治性中枢神经系统弥漫性大B细胞淋巴瘤患者的结局。
纳入的37例患者中,11例接受了Ore-MTD治疗,26例接受了Ore-MIED方案治疗。我们队列中的总缓解率为89.2%,51.4%的患者实现完全缓解,37.8%的患者实现部分缓解。观察到的无进展生存期中位数为7.0个月。接受不同治疗方案的患者之间的无进展生存期中位数无统计学显著差异(Ore-MTD为5.0个月,Ore-MIED为13.0个月;P = 0.29)。此外,该队列的总生存期中位数尚未达到,这表明尽管疾病具有侵袭性,但预后良好。
我们的研究证实了Ore-MIED/Ore-MTD在rrCNSL患者中的有效性和安全性,即使是那些先前接受过多种治疗方案的患者。