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A single institutional retrospective evaluation for younger patients withprimary central nervous lymphomas on a modified R-MPV regimen followed by radiotherapy andhigh dose cytarabine

机译:对年轻患者进行单一机构回顾性评估采用改良的R-MPV方案的原发性中枢神经淋巴瘤然后进行放射治疗和大剂量阿糖胞苷

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摘要

We conducted a retrospective analysis of patients younger than 60 years (N = 10, median age 54.5) with newly diagnosed primary central nervous system lymphoma (PCNSL) at the University of Tsukuba Hospital from January 2008 to November 2016. All the patients were scheduled to receive a single regimen without registration to any clinical trials. This was based on a phase 2 study by Memorial Sloan-Kettering Cancer Center (MSKCC); induction chemotherapy with rituximab, methotrexate, procarbazine, and vincristine (R-MPV) (five to seven cycles), followed by whole-brain radiotherapy (rd-WBRT) (23.4 Gy) and two high-dose cytarabine (HD-AC) cycles as a consolidation. The median age was 54.5 years, and median follow up duration was 33.1 months. The 3-year overall survival (OS) and progression-free survival (PFS) were 69% (95% CI 31–89%) and 56% (95% CI 20–81%). The median OS and PFS were not reached, respectively. Acute and delayed toxicities were manageable. In particular, OS and PFS of seven patients who achieved CR by the R-MPV induction chemotherapy were significantly superb (3-year OS, 100%; 3-year PFS, 80%), implying that a large proportion of patients in CR after the completion of this treatment may achieve durable disease control.On the other hand, all of the three patients who had progressive disease during this treatment died of disease progression within 1 year after diagnosis without achieving CR. Identifying the patients having a risk of failure in the R-MPV induction chemotherapy isimportant, and may allow us to consider a potentially more effective regimen.
机译:我们于2008年1月至2016年11月在筑波大学医院对60岁以下(N = 10,中位年龄54.5)新诊断的原发性中枢神经系统淋巴瘤(PCNSL)的患者进行了回顾性分析。无需接受任何临床试验即可接受单一方案。这是基于纪念斯隆-凯特琳癌症中心(MSKCC)的第二阶段研究得出的;利妥昔单抗,甲氨蝶呤,丙卡巴肼和长春新碱(R-MPV)诱导化疗(5至7个周期),然后进行全脑放射治疗(rd-WBRT)(23.4 Gy)和两个大剂量阿糖胞苷(HD-AC)周期作为合并。中位年龄为54.5岁,中位随访时间为33.1个月。 3年总生存期(OS)和无进展生存期(PFS)分别为69%(95%CI 31-89%)和56%(95%CI 20-81%)。分别未达到OS和PFS的中位数。急性和延迟毒性是可以控制的。尤其是,通过R-MPV诱导化疗获得CR的7例患者的OS和PFS显着优异(3年OS,100%; 3年PFS,80%),这意味着在CR后的CR患者中有很大一部分另一方面,在此治疗过程中进行性疾病的三名患者在诊断后一年之内都死于疾病进展,而未达到CR。确定在R-MPV诱导化疗中失败的患者是重要,并且可以使我们考虑可能更有效的治疗方案。

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