Puckrin Robert, Stewart Colin, Owen Carolyn, Street Lesley E, Perry Sarah, Duggan Peter, Shafey Mona, Chua Neil, Stewart Douglas A
Tom Baker Cancer Centre and University of Calgary, Calgary, Canada.
Tom Baker Cancer Centre and University of Calgary, Calgary, Canada.
Clin Lymphoma Myeloma Leuk. 2025 Apr;25(4):265-270. doi: 10.1016/j.clml.2024.11.008. Epub 2024 Dec 13.
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.
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.
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.
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.
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。
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)。
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。
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。