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大剂量化疗后自体造血干细胞移植作为原发性中枢神经系统淋巴瘤一线治疗的预后 - 一项长期随访研究。

Prognosis after high-dose chemotherapy followed by autologous stem-cell transplantation as first-line treatment in primary CNS lymphoma--a long-term follow-up study.

机构信息

Department of Hematology and Oncology, University Medical Center Freiburg, Freiburg, Germany; Basel Institute for Clinical Epidemiology and Biostatistics, University Hospital Basel, Basel, Switzerland.

Department of Hematology and Oncology, University Medical Center Freiburg, Freiburg, Germany.

出版信息

Ann Oncol. 2012 Oct;23(10):2670-2675. doi: 10.1093/annonc/mds059. Epub 2012 Apr 3.

Abstract

BACKGROUND

High-dose chemotherapy followed by autologous stem-cell transplantation (HCT-ASCT) is a promising approach in eligible patients with primary central nervous system lymphoma (PCNSL). We report long-term data of patients who were treated according to HCT-ASCT containing protocols.

PATIENTS AND METHODS

We analyzed survival and relapse rates in 43 (<67 years) immunocompetent patients with newly diagnosed PCNSL being treated according to two different high-dose methotrexate-based protocols followed by high-dose carmustine/thiotepa (BCNU/TT) plus ASCT (±whole brain irradiation). Analysis was conducted for all patients (intention-to-treat) and those patients who actually received HCT-ASCT (per-protocol).

RESULTS

Thirty-four patients achieved complete remission, of those 12 relapsed (35%), while 6 of them relapsed 5 years after diagnosis. After a median follow-up of 120 months, median overall survival (OS) was reached after 104 months. Two- and 5-year OS was 81% and 70% and 2- and 5-year event-free survival (EFS) was 81% and 67%, respectively. In per-protocol analysis (N = 34), 5-year OS and EFS was 82% and 79%, respectively. HCT-ASCT associated related mortality was not observed.

CONCLUSIONS

Sequential high-dose MTX containing chemotherapy followed by high-dose carmustine/thiotepa plus ASCT (±whole brain irradiation) is safe and leads to high survival rates in eligible patients with newly diagnosed PCNSL.

摘要

背景

对于符合条件的原发性中枢神经系统淋巴瘤(PCNSL)患者,大剂量化疗后自体造血干细胞移植(HCT-ASCT)是一种很有前途的治疗方法。我们报告了根据包含 HCT-ASCT 的方案治疗的患者的长期数据。

患者和方法

我们分析了根据两种不同的大剂量甲氨蝶呤为基础的方案治疗的 43 名(<67 岁)免疫功能正常的新诊断为 PCNSL 患者的生存和复发率,这些患者随后接受了大剂量卡莫司汀/噻替哌(BCNU/TT)加 ASCT(±全脑照射)。对所有患者(意向治疗)和实际接受 HCT-ASCT 的患者(方案治疗)进行了分析。

结果

34 例患者达到完全缓解,其中 12 例复发(35%),其中 6 例在诊断后 5 年复发。中位随访 120 个月后,中位总生存期(OS)在 104 个月时达到。2 年和 5 年 OS 分别为 81%和 70%,2 年和 5 年无事件生存率(EFS)分别为 81%和 67%。在方案治疗分析(N=34)中,5 年 OS 和 EFS 分别为 82%和 79%。未观察到与 HCT-ASCT 相关的死亡。

结论

序贯大剂量 MTX 为基础的化疗后接受大剂量卡莫司汀/噻替哌加 ASCT(±全脑照射)在适合的新诊断为 PCNSL 的患者中是安全的,并导致高生存率。

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