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弥漫性大 B 细胞淋巴瘤的中枢神经系统预防策略。

Central Nervous System Prophylaxis Strategies in Diffuse Large B Cell Lymphoma.

机构信息

Department of Internal Medicine, Section of Medical Oncology/Hematology, CancerCare Manitoba, University of Manitoba, 409 Tache Avenue, Winnipeg, MB, R2H 2A6, Canada.

出版信息

Curr Treat Options Oncol. 2018 Sep 10;19(11):52. doi: 10.1007/s11864-018-0569-2.

Abstract

Central nervous system (CNS) relapse is an undesirable event in the course of patients with diffuse large B cell lymphoma (DLBCL) with a median survival of approximately 6 months following CNS relapse. CNS prophylaxis for the prevention of CNS recurrence, in addition to the standard R-CHOP chemotherapy, is thus preferable. For an overall relapse risk of 2-5%, administration of CNS-directed therapies for all patients with DLBCL is unnecessary and prophylaxis should be targeted for the high-risk patients. CNS-International Prognostic Index (CNS-IPI) score has enabled risk stratification with risk ranging < 1% (low-risk group) compared to > 10% (high-risk group). The latter could be considered for CNS prophylaxis. CNS-IPI, however, is not perfect and may not capture patients with high-risk extra-nodal sites such as testicular DLBCL. Cell-of-origin and MYC/BCL2 expression can further build on CNS-IPI to narrow higher risk patients. CNS prophylaxis strategies are controversial. Common strategies include intrathecal (IT) chemotherapy and systemic CNS penetrants such as methotrexate. IT chemotherapy does not adequately penetrate the brain parenchyma and hence it is insufficient in preventing parenchymal CNS recurrences. Most experts promote systemic methotrexate for high-risk groups, which penetrates both the leptomeningeal and parenchymal CNS compartments. Even though systemic CNS prophylaxis is widely promoted over IT alone, its efficacy is unclear. Ongoing efforts in search for appropriate CNS prophylaxis strategies are warranted. My personal practice is to administer systemic high-dose methotrexate in conjunction with R-CHOP chemotherapy for eligible patients deemed at a high risk of CNS recurrence, especially those with high-risk CNS-IPI and extra-nodal involvement.

摘要

中枢神经系统 (CNS) 复发是弥漫性大 B 细胞淋巴瘤 (DLBCL) 患者病程中的不良事件,CNS 复发后患者的中位生存时间约为 6 个月。因此,除了标准的 R-CHOP 化疗外,CNS 预防对于预防 CNS 复发是优选的。对于总体复发风险为 2-5%的患者,对于所有 DLBCL 患者使用 CNS 定向治疗是不必要的,预防应针对高危患者。中枢神经系统国际预后指数 (CNS-IPI) 评分可进行风险分层,风险范围为 <1%(低危组)与 >10%(高危组)。后者可考虑 CNS 预防。然而,CNS-IPI 并不完美,可能无法捕获具有高危结外部位的患者,如睾丸 DLBCL。细胞起源和 MYC/BCL2 表达可以进一步构建 CNS-IPI 以缩小高危患者范围。CNS 预防策略存在争议。常见策略包括鞘内 (IT) 化疗和全身穿透 CNS 的药物,如甲氨蝶呤。IT 化疗不能充分穿透脑实质,因此不足以预防实质 CNS 复发。大多数专家提倡高危患者使用全身甲氨蝶呤,因为它可以穿透软脑膜和实质 CNS 腔室。尽管系统的 CNS 预防比单独使用 IT 更为广泛,但它的疗效尚不清楚。有必要进行进一步的研究来寻找合适的 CNS 预防策略。我个人的做法是为有高 CNS 复发风险的合格患者(尤其是具有高危 CNS-IPI 和结外受累的患者)在接受 R-CHOP 化疗的同时给予全身大剂量甲氨蝶呤。

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