Angelov Lilyana, Doolittle Nancy D, Kraemer Dale F, Siegal Tali, Barnett Gene H, Peereboom David M, Stevens Glen, McGregor John, Jahnke Kristoph, Lacy Cynthia A, Hedrick Nancy A, Shalom Edna, Ference Sandra, Bell Susan, Sorenson Lisa, Tyson Rose Marie, Haluska Marianne, Neuwelt Edward A
3181 SW Sam Jackson Park Rd, Mailcode L603, Portland, OR 97239, USA.
J Clin Oncol. 2009 Jul 20;27(21):3503-9. doi: 10.1200/JCO.2008.19.3789. Epub 2009 May 18.
PURPOSE Primary CNS lymphoma (PCNSL) is confined to the CNS and/or the eyes at presentation and is usually initially treated with intravenous methotrexate-based chemotherapy and whole-brain radiotherapy (WBRT). However, the intact blood-brain barrier (BBB) can limit diffusion of methotrexate into brain and tumor. With BBB disruption (BBBD), enhanced drug delivery to the tumor can be achieved. PATIENTS AND METHODS This report summarizes the multi-institutional experience of 149 newly diagnosed (with no prior WBRT) patients with PCNSL treated with osmotic BBBD and intra-arterial (IA) methotrexate at four institutions from 1982 to 2005. In this series, 47.6% of patients were age > or = 60 years, and 42.3% had Karnofsky performance score (KPS) less than 70 at diagnosis. Results The overall response rate was 81.9% (57.8% complete; 24.2% partial). Median overall survival (OS) was 3.1 years (25% estimated survival at 8.5 years). Median progression-free survival (PFS) was 1.8 years, with 5-year PFS of 31% and 7-year PFS of 25%. In low-risk patients (age < 60 years and KPS > or = 70), median OS was approximately 14 years, with a plateau after approximately 8 years. Procedures were generally well tolerated; focal seizures (9.2%) were the most frequent side effect and lacked long-term sequelae. CONCLUSION This large series of patients treated over a 23-year period demonstrates that BBBD/IA methotrexate-based chemotherapy results in successful and durable tumor control and outcomes that are comparable or superior to other PCNSL treatment regimens.
目的 原发性中枢神经系统淋巴瘤(PCNSL)在初诊时局限于中枢神经系统和/或眼部,通常最初采用以静脉注射甲氨蝶呤为主的化疗和全脑放疗(WBRT)。然而,完整的血脑屏障(BBB)会限制甲氨蝶呤向脑和肿瘤的扩散。通过破坏血脑屏障(BBBD),可实现向肿瘤的药物递送增强。
患者与方法 本报告总结了1982年至2005年期间在四家机构对149例新诊断(未接受过WBRT)的PCNSL患者进行渗透性BBBD和动脉内(IA)甲氨蝶呤治疗的多机构经验。在该系列中,47.6%的患者年龄≥60岁,42.3%的患者在诊断时卡诺夫斯基表现评分(KPS)低于70。
结果 总缓解率为81.9%(完全缓解57.8%;部分缓解24.2%)。中位总生存期(OS)为3.1年(8.5年时估计生存率为25%)。中位无进展生存期(PFS)为1.8年,5年PFS为31%,7年PFS为25%。在低风险患者(年龄<60岁且KPS≥70)中,中位OS约为14年,约8年后出现平台期。手术一般耐受性良好;局灶性癫痫发作(9.2%)是最常见的副作用,且无长期后遗症。
结论 这一在23年期间治疗的大量患者系列表明,基于BBBD/IA甲氨蝶呤的化疗可成功且持久地控制肿瘤,其结果与其他PCNSL治疗方案相当或更优。