Division of Hematology/Oncology, Helen Diller Comprehensive Cancer Center University of California, San Francisco, CA, USA.
Br J Haematol. 2014 Aug;166(3):311-25. doi: 10.1111/bjh.12938. Epub 2014 May 16.
Until recently, primary central nervous system lymphoma (PCNSL) was associated with a uniformly dismal prognosis. It is now reasonable to anticipate long-term survival and possibly cure for a significant proportion of patients diagnosed with PCNSL. Accumulated data generated over the past 10 years has provided evidence that long-term progression-free survival (PFS) can reproducibly be attained in a significant fraction of PCNSL patients that receive dose-intensive chemotherapy consolidation, without whole brain radiotherapy. One consolidative regimen that has reproducibly demonstrated promise is the combination of infusional etoposide plus high-dose cytarabine (EA), administered in first complete remission after methotrexate, temozolomide and rituximab-based induction. Given evolving principles of management and the mounting evidence for reproducible improvements in survival rates in prospective clinical series, our goal in this review is to highlight and update principles in diagnosis, staging and management as well as to review data regarding the pathogenesis of central nervous system lymphomas, information that is likely to constitute a basis for the implementation of novel therapies that are requisite for further progress in this unique phenotype of non-Hodgkin lymphoma.
直到最近,原发性中枢神经系统淋巴瘤(PCNSL)的预后一直很差。现在,相当一部分被诊断为 PCNSL 的患者有望长期生存甚至治愈。过去 10 年来积累的数据提供了证据,表明在不进行全脑放疗的情况下,接受剂量密集型化疗巩固治疗的 PCNSL 患者中,可重复性地实现长期无进展生存(PFS)。一种已经证明有希望的巩固方案是在甲氨蝶呤、替莫唑胺和利妥昔单抗诱导后完全缓解时,输注依托泊苷加高剂量阿糖胞苷(EA)的联合方案。鉴于管理原则的不断发展以及前瞻性临床系列中生存率可重复性提高的证据,我们在这篇综述中的目标是强调和更新诊断、分期和管理原则,并回顾有关中枢神经系统淋巴瘤发病机制的数据,这些信息可能构成实施新疗法的基础,而这些新疗法是在这种独特的非霍奇金淋巴瘤表型中取得进一步进展所必需的。