原发性中枢神经系统淋巴瘤:正在进行的临床试验的叙述性回顾和未来研究的目标。

Lauren R Schaff, Prakash Ambady, Nancy D Doolittle, Christian Grommes
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引用次数: 5

摘要

原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的脑、脊柱、脑脊液(CSF)和/或玻璃体视网膜间隙疾病。PCNSL对化疗和放射敏感,但在最初治疗数年后复发是常见的。除了使用高剂量甲氨蝶呤(HD-MTX)作为一线治疗的共识之外,在新诊断或复发的PCNSL的管理方面几乎没有一致性。缺乏共识是由于缺乏对这种疾病的随机试验。前瞻性研究受到低入组率、缺乏标准的诱导方案以及整合策略的不同方法的困扰。此外,PCNSL患者群体是异质性的,包括高比例的老年或体弱患者,并由中枢神经系统(CNS)不同室的疾病患者组成。因此,目前的治疗策略差异很大,往往由医生和机构的偏好或地区实践决定。本文综述了最近完成的和正在进行的针对新诊断和复发或难治性PCNSL患者的治疗研究。它讨论了诱导和巩固或维持方案的常见方法背后的现有证据以及有关复发性疾病管理的最新数据。最后,它强调了该疾病试验设计的复杂性,并为未来研究的设计提供了一个框架,这些研究需要确定可能从特定诱导、巩固或维持治疗中受益的患者群体。
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Primary central nervous system lymphoma: a narrative review of ongoing clinical trials and goals for future studies.

Primary central nervous system lymphoma (PCNSL) is a rare disease of the brain, spine, cerebrospinal fluid (CSF) and/or vitreoretinal space. PCNSL is chemo and radiosensitive but relapse is common even years after initial treatment. Outside of consensus regarding the use of high-dose methotrexate (HD-MTX) for first line treatment, there is little uniformity in the management of newly diagnosed or relapsed PCNSL. The lack of consensus is driven by a paucity of randomized trials in this disease. Prospective studies are troubled by low enrollment, the lack of a standard induction regimen, and a varied approach to consolidation strategies. Moreover, the PCNSL patient population is heterogeneous and includes a high proportion of elderly or frail patients and consists of patients manifesting disease in varied compartments of the central nervous system (CNS). As a result, current treatment strategies vary widely and are often dictated by physician and institutional preference or regional practice. This review provides an overview of recently completed and ongoing therapeutic studies for patients with newly diagnosed and recurrent or refractory PCNSL. It discusses the existing evidence behind common approaches to induction and consolidation or maintenance regimens as well as the recent data regarding management of recurrent disease. Finally, it highlights the complexity of trial design in this disease and provides a framework for the design of future studies, which are needed to identify patient populations likely to benefit from specific induction, consolidation, or maintenance therapies.

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