Department of Neuro-Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Department of Hematology, Middlemore Hospital, Auckland, New Zealand.
Neuro Oncol. 2024 Apr 5;26(4):724-734. doi: 10.1093/neuonc/noad224.
BACKGROUND: Studies on the efficacy of rituximab in primary CNS lymphoma (PCNSL) reported conflicting results. Our international randomized phase 3 study showed that the addition of rituximab to high-dose methotrexate, BCNU, teniposide, and prednisolone (MBVP) in PCNSL was not efficacious in the short term. Here we present long-term results after a median follow-up of 82.3 months. METHODS: One hundred and ninety-nine eligible newly diagnosed, nonimmunocompromised patients with PCNSL aged 18-70 years with WHO performance status 0-3 was randomized between treatment with MBVP chemotherapy with or without rituximab, followed by high-dose cytarabine consolidation in responding patients, and reduced-dose WBRT in patients aged ≤ 60 years. Event-free survival was the primary endpoint. Overall survival rate, neurocognitive functioning (NCF), and health-related quality of life (HRQoL) were additionally assessed, with the IPCG test battery, EORTC QLQ-C30 and QLQ-BN20 questionnaires, respectively. RESULTS: For event-free survival, the hazard ratio was 0.85, 95% CI 0.61-1.18, P = .33. Overall survival rate at 5 years for MBVP and R-MBVP was 49% (39-59) and 53% (43-63) respectively. In total, 64 patients died in the MBVP arm and 55 in the R-MBVP arm, of which 69% were due to PCNSL. At the group level, all domains of NCF and HRQoL improved to a clinically relevant extent after treatment initiation, and remained stable thereafter up to 60 months of follow-up, except for motor speed which deteriorated between 24 and 60 months. Although fatigue improved initially, high levels persisted in the long term. CONCLUSIONS: Long-term follow-up confirms the lack of added value of rituximab in addition to MBVP and HD-cytarabine for PCNSL.
背景:关于利妥昔单抗治疗原发性中枢神经系统淋巴瘤(PCNSL)的疗效,已有研究结果相互矛盾。我们的国际多中心 3 期随机临床试验显示,在 PCNSL 患者中,利妥昔单抗联合大剂量甲氨蝶呤、BCNU、依托泊苷和泼尼松(MBVP)方案治疗在短期内并无疗效。在此,我们报道中位随访 82.3 个月后的长期结果。
方法:199 例年龄在 18-70 岁、未经免疫抑制治疗、世界卫生组织体力状态评分为 0-3 分的新诊断非免疫功能低下的 PCNSL 患者,按 1:1 随机分组,分别接受 MBVP 化疗联合或不联合利妥昔单抗治疗,随后对缓解患者行大剂量阿糖胞苷巩固治疗,年龄≤60 岁患者行低剂量全脑放疗。无进展生存期为主要终点。此外,还评估了总生存率、神经认知功能(NCF)和健康相关生活质量(HRQoL),采用国际 PCNSL 协作组测试组合、EORTC QLQ-C30 和 QLQ-BN20 问卷分别进行评估。
结果:无进展生存的风险比为 0.85,95%置信区间为 0.61-1.18,P=0.33。MBVP 和 R-MBVP 组的 5 年总生存率分别为 49%(39-59)和 53%(43-63)。MBVP 组和 R-MBVP 组共有 64 例和 55 例患者死亡,其中 69%的死亡原因为 PCNSL。在组水平上,所有 NCF 和 HRQoL 领域在治疗开始后均得到了显著改善,且在 60 个月随访期内保持稳定,除了运动速度在 24-60 个月之间恶化外。尽管疲劳症状最初得到改善,但在长期随访中仍持续存在。
结论:长期随访结果证实,在 MBVP 和 HD-阿糖胞苷治疗的基础上,添加利妥昔单抗对 PCNSL 并无额外获益。
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