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在 ALL 型诱导治疗时代 T 细胞淋巴母细胞淋巴瘤行造血干细胞移植预处理的适应证和获益

Indication and benefit of upfront hematopoietic stem cell transplantation for T-cell lymphoblastic lymphoma in the era of ALL-type induction therapies.

机构信息

Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Department of Hematology, Kobe City Medical Center General Hospital, Hyogo, Japan.

出版信息

Sci Rep. 2020 Dec 8;10(1):21418. doi: 10.1038/s41598-020-78334-x.

Abstract

Since the introduction of leukemia-type induction therapies for T-cell lymphoblastic lymphoma (T-LBL), improvements in the long-term outcomes of T-LBL have been reported. However, indications for and the appropriate timing of hematopoietic stem cell transplantation (HSCT) have not yet been established. Therefore, we performed a multicenter retrospective cohort study of patients with T-LBL treated using leukemia-type initial therapies to compare the outcomes after HSCT at different disease stages. We enrolled 21 patients with T-LBL from a total of 11 centers, and all patients received hyper-CVAD as a leukemia-type initial regimen. HSCT was performed during the CR1/PR1 (standard disease) stage in 11 patients, while it was completed at a later or non-remission (advanced disease) stage in 10 patients. Following HSCT, the overall survival rate was significantly greater in standard disease than in advanced-disease patients (79.5% vs. 30.0% at 5 years; hazard ratio (HR) 5.97; p = 0.03), with trend to the lower incidence of relapse in the former group (27.3% vs. 60.0% at 5 years; HR 2.29; p = 0.19). A prognostic difference was not detected between cases treated with allogeneic and autologous HSCTs. Our study suggests that frontline HSCT may be a feasible treatment option for T-LBL, even in the era of leukemia-type initial therapy.

摘要

自采用白血病型诱导疗法治疗 T 细胞淋巴母细胞淋巴瘤(T-LBL)以来,T-LBL 的长期预后得到了改善。然而,造血干细胞移植(HSCT)的适应证和合适时机尚未确定。因此,我们对采用白血病型初始疗法治疗的 T-LBL 患者进行了多中心回顾性队列研究,比较了不同疾病阶段 HSCT 后的结果。我们从总共 11 个中心招募了 21 例 T-LBL 患者,所有患者均接受 Hyper-CVAD 作为白血病型初始方案。11 例患者在 CR1/PR1(标准疾病)期进行 HSCT,10 例患者在晚期或未缓解(进展期疾病)期完成 HSCT。HSCT 后,标准疾病患者的总生存率显著高于进展期疾病患者(5 年时分别为 79.5%和 30.0%;HR 5.97;p=0.03),前者的复发率也呈下降趋势(5 年时分别为 27.3%和 60.0%;HR 2.29;p=0.19)。异基因和自体 HSCT 治疗的病例之间未发现预后差异。我们的研究表明,一线 HSCT 可能是 T-LBL 的一种可行治疗选择,即使在采用白血病型初始治疗的时代也是如此。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46f8/7722931/5e5170929b71/41598_2020_78334_Fig1_HTML.jpg

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