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原发中枢弥漫性大 B 细胞淋巴瘤患者行自体造血干细胞移植时,噻替哌剂量强度对其与卡莫司汀联合预处理方案的影响。

Impact of thiotepa dose-intensity in primary diffuse large B-cell lymphoma of the central nervous system undergoing autologous hematopoietic cell transplant with thiotepa/carmustine conditioning.

机构信息

School of Medicine, University of Kentucky, Lexington, KY, USA.

Division of Biostatistics, Institute for Health and Equity, Medical College of Wisconsin, Milwaukee, WI, USA.

出版信息

Bone Marrow Transplant. 2023 Nov;58(11):1203-1208. doi: 10.1038/s41409-023-02071-8. Epub 2023 Aug 10.

DOI:10.1038/s41409-023-02071-8
PMID:37563283
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11078515/
Abstract

Thiotepa/carmustine (TT-BCNU) is a commonly used autologous transplant (ASCT) conditioning regimen for primary DLBCL of the CNS (PCNSL). The total thiotepa dose varies among TT-BCNU recipients, with some centers administering a total dose of 20 mg/kg, while others using 10 mg/kg. We retrospectively assessed the impact of thiotepa dose intensity on ASCT outcomes in 218 adult PCNSL patients who underwent a first ASCT with TT-BCNU conditioning and received either a total thiotepa dose of 10 mg/kg (TT-10 group; N = 90), or 20 mg/kg (TT-20 group; N = 128). The median follow-up of survivors was 22 months. The cumulative incidence of 1-year non-relapse mortality (NRM) for TT-10 and TT-20 cohorts were 6% (95%CI = 2-12%) vs. 4% (95%CI = 1-8%), respectively (p = 0.66). The 3-year cumulative incidence of relapse (15% vs. 13%; p = 0.67), progression-free survival (PFS) (71% vs. 80%; p = 0.25) and overall survival (OS) (79% vs. 83%; p = 0.56) were similar in the TT-10 and TT-20 groups, respectively. On multivariate analysis compared to TT-10, the TT-20 cohort was not associated with significantly different risk of NRM (Hazard ration [HR] = 0.77; p = 0.64), relapse/progression (HR = 0.87; p = 0.74), PFS (HR = 0.80; p = 0.48) or OS (HR = 1.10; p = 0.80). In conclusion thiotepa dose-intensity in TT-BCNU conditioning does not impact ASCT outcomes of PCNSL patients.

摘要

噻替派/卡莫司汀(TT-BCNU)是原发性中枢神经系统弥漫性大 B 细胞淋巴瘤(PCNSL)患者常用的自体移植(ASCT)预处理方案。TT-BCNU 接受者的噻替派总剂量不同,一些中心给予 20mg/kg 的总剂量,而其他中心则使用 10mg/kg。我们回顾性评估了 218 例接受 TT-BCNU 预处理的首次 ASCT 的成年 PCNSL 患者的噻替派剂量强度对 ASCT 结果的影响,这些患者接受了 10mg/kg(TT-10 组;N=90)或 20mg/kg(TT-20 组;N=128)的总噻替派剂量。幸存者的中位随访时间为 22 个月。TT-10 和 TT-20 队列的 1 年非复发死亡率(NRM)累积发生率分别为 6%(95%CI=2-12%)和 4%(95%CI=1-8%)(p=0.66)。TT-10 和 TT-20 组的 3 年累积复发率(15%比 13%;p=0.67)、无进展生存率(PFS)(71%比 80%;p=0.25)和总生存率(OS)(79%比 83%;p=0.56)相似。与 TT-10 相比,多变量分析显示 TT-20 队列与 NRM(风险比 [HR]=0.77;p=0.64)、复发/进展(HR=0.87;p=0.74)、PFS(HR=0.80;p=0.48)或 OS(HR=1.10;p=0.80)的风险无显著差异。总之,TT-BCNU 预处理中噻替派的剂量强度不影响 PCNSL 患者的 ASCT 结果。

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