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降阶梯诱导治疗及基于噻替派/白消安的自体干细胞移植治疗原发性中枢神经系统淋巴瘤

De-escalated Induction Therapy and Thiotepa/Busulfan-based Autologous Stem Cell Transplantation for Primary Central Nervous System Lymphoma.

作者信息

Puckrin Robert, Stewart Colin, Owen Carolyn, Street Lesley E, Perry Sarah, Duggan Peter, Shafey Mona, Chua Neil, Stewart Douglas A

机构信息

Tom Baker Cancer Centre and University of Calgary, Calgary, Canada.

Tom Baker Cancer Centre and University of Calgary, Calgary, Canada.

出版信息

Clin Lymphoma Myeloma Leuk. 2025 Apr;25(4):265-270. doi: 10.1016/j.clml.2024.11.008. Epub 2024 Dec 13.

Abstract

BACKGROUND

Thiotepa-based autologous stem cell transplantation (ASCT) improves survival in primary central nervous system lymphoma (PCNSL), but > 30% of patients are unable to undergo ASCT following commonly used intensive induction regimens.

METHODS

This retrospective population-based study included consecutive patients ≥ 18 years old with PCNSL who were intended for ASCT in Alberta, Canada between 2011 and 2022. A reduced-intensity induction protocol was further abbreviated in 2018 to decrease toxicity and expediate ASCT by incorporating rituximab, procarbazine, and only 2 doses of high-dose methotrexate and 1 cycle of high-dose cytarabine before consolidation with thiotepa-busulfan conditioning. Progression-free survival (PFS) and overall survival (OS) were determined using the Kaplan-Meier method.

RESULTS

Among 71 patients with median age 58 years (range 26-72), ASCT was completed in 56 (79%), with the transplantation rate among patients > 60 years old increasing by 30% following the abbreviation of induction therapy. With median follow-up time 3.9 years, 4-year PFS and OS were 69% (95% CI 56%-79%) and 80% (95% CI 67%-88%) for all patients and 75% (95% CI 57%-86%) and 85% (95% CI 68%-93%) for ASCT recipients, respectively. There was 1 death due to treatment-related mortality during induction and none after ASCT, including among 17 transplanted patients > 60 years old.

CONCLUSION

An abbreviated induction regimen followed by thiotepa-busulfan-based ASCT achieves high transplantation rates with low risks of relapse and treatment-related mortality, thereby providing an effective treatment strategy for PCNSL.

摘要

背景

基于噻替派的自体干细胞移植(ASCT)可提高原发性中枢神经系统淋巴瘤(PCNSL)患者的生存率,但采用常用的强化诱导方案后,超过30%的患者无法进行ASCT。

方法

这项基于人群的回顾性研究纳入了2011年至2022年期间加拿大艾伯塔省连续的年龄≥18岁且计划进行ASCT的PCNSL患者。2018年,一种降低强度的诱导方案进一步简化,通过加入利妥昔单抗、丙卡巴肼,以及在使用噻替派-白消安预处理进行巩固之前仅使用2剂高剂量甲氨蝶呤和1周期高剂量阿糖胞苷,以降低毒性并加快ASCT进程。采用Kaplan-Meier方法确定无进展生存期(PFS)和总生存期(OS)。

结果

在71例中位年龄为58岁(范围26 - 72岁)的患者中,56例(79%)完成了ASCT,诱导治疗简化后,60岁以上患者的移植率提高了30%。中位随访时间为3.9年,所有患者的4年PFS和OS分别为69%(95%CI 56% - 79%)和80%(95%CI 67% - 88%),ASCT接受者分别为75%(95%CI 57% - 86%)和85%(95%CI 68% - 93%)。诱导期间有1例因治疗相关死亡率死亡,ASCT后无死亡病例,包括17例60岁以上的移植患者。

结论

采用简化诱导方案后进行基于噻替派-白消安的ASCT可实现高移植率,且复发风险和治疗相关死亡率低,从而为PCNSL提供了一种有效的治疗策略。

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