Effectiveness and safety of orelabrutinib combined with rituximab, temozolomide, methotrexate, and cytarabine in intensive chemotherapy-unfit patients with PCNSL in China

在中国,奥拉替尼联合利妥昔单抗、替莫唑胺、甲氨蝶呤和阿糖胞苷治疗不适合接受强化化疗的原发性中枢神经系统淋巴瘤患者的疗效和安全性研究

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Abstract

BACKGROUND: Primary central nervous system lymphoma (PCNSL) is a rare and aggressive lymphoma subtype. Orelabrutinib (O), a novel and potent second-generation Bruton tyrosine kinase inhibitor, has shown impressive efficacy in PCNSL. This study aimed to evaluate the effectiveness and safety of the O-based regimen in the treatment of intensive chemotherapy-unfit patients with newly diagnosed PCNSL. METHODS: In this single-center, retrospective case series, we consecutively included 10 patients with PCNSL who were unfit for intensive chemotherapy, defined as an Eastern Cooperative Oncology Group performance status score of ≥ 3, a Karnofsky Performance Status score of ≤ 70, or a Sequential Organ Failure Assessment score of ≥ 2. All patients received the O-based regimen, including the combination of O, rituximab (R), and temozolomide (T; ORT), with or without methotrexate (M) or cytarabine (A; ORT-M/A), followed by ORT maintenance. The effectiveness outcomes were overall response rate (ORR), progression-free survival (PFS), and overall survival (OS). RESULTS: Following ORT-M/A treatment, six patients achieved a complete response (60.0% [95% CI 26.2-87.8]) and four achieved a partial response, yielding an ORR of 100.0% (95% CI 69.2-100.0). As of the data cutoff (September 7, 2025), the median follow-up of 23.7 months (range, 9.2-40.2). The corresponding 24-month PFS rate and 36-month OS rate were 80.0% (95% CI 51.6-100.0) and 90.0% (95% CI 73.2-100.0), respectively. The most common grade 3-4 treatment-related adverse events (AEs) were thrombocytopenia (100.0%) and leukopenia (90.0%). No serious AEs or treatment-related deaths were observed. CONCLUSION: The ORT-M/A chemotherapy regimen was efficacious and well-tolerated in our patients with PCNSL. This retrospective study provided a potential therapeutic strategy for PCNSL patients who are unfit for intensive chemotherapy and warrant further investigation.

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