首页> 外文期刊>Annals of Hematology >Allogeneic stem cell transplantation in patients with non-Hodgkin lymphoma who experienced relapse or progression after autologous stem cell transplantation
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Allogeneic stem cell transplantation in patients with non-Hodgkin lymphoma who experienced relapse or progression after autologous stem cell transplantation

机译:自体干细胞移植后复发或进展的非霍奇金淋巴瘤患者的同种异体干细胞移植

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摘要

There are few treatment options for patients with non-Hodgkin lymphoma (NHL) who experienced progression after high-dose chemotherapy (HDC) with autologous stem cell transplantation (auto-SCT). The role of allogeneic stem cell transplantation (allo-SCT) in these patients has not been clarified yet. In this study, we report clinical outcomes of allo-SCT in patients with NHL who experienced progression after HDC with auto-SCT. Patients were enrolled from seven hospitals in Korea. A total of 38 patients were included: 18 patients (47.4%) underwent myeloablative conditioning and 20 patients (52.6%) reduced intensity conditioning. Overall response rate was 73.3%. Median event-free survival was 6.3 months. Median overall survival (OS) was 19.0 months. Estimated 5-year survival rate was 35.0%. Acute graft-versus-host disease developed in 13 patients (34.2%). Transplant-related mortality (TRM) was 21.1% (eight patients). Ann Arbor stage (p = 0.022), performance status (p < 0.001), and baseline serum albumin level (p = 0.010) were significant risk factors for OS. Performance status (p = 0.022) was a significant risk factor for TRM. Eight patients with persistent or progressive disease received donor lymphocyte infusion, and two of them achieved complete remission. In conclusion, despite high TRM, allo-SCT is a viable option for patients with NHL who underwent progression after HDC with auto-SCT.
机译:对于非霍奇金淋巴瘤(NHL)在大剂量化疗(HDC)和自体干细胞移植(auto-SCT)后进展的患者,几乎没有治疗选择。异基因干细胞移植(allo-SCT)在这些患者中的作用尚未阐明。在这项研究中,我们报告了在用自动SCT进行HDC后进展的NHL患者中,使用allo-SCT的临床结局。患者来自韩国的七家医院。总共包括38例患者:18例(47.4%)接受了清髓治疗,20例(52.6%)进行了强度减弱治疗。总体回应率为73.3%。无事件生存的中位数为6.3个月。中位总生存期(OS)为19.0个月。估计5年生存率为35.0%。 13例患者发生了急性移植物抗宿主病(34.2%)。移植相关死亡率(TRM)为21.1%(8例患者)。 Ann Arbor分期(p = 0.022),表现状态(p <0.001)和基线血清白蛋白水平(p = 0.010)是OS的重要危险因素。绩效状态(p = 0.022)是TRM的重要危险因素。患有持续性或进行性疾病的8例患者接受了供体淋巴细胞输注,其中2例完全缓解。总之,尽管TRM较高,但对于自体SCT进行HDC后进展的NHL患者,异体SCT是可行的选择。

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