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异基因干细胞移植在复发或难治性霍奇金淋巴瘤中的作用。

Role of allogeneic stem cell transplantation in relapsed or refractory Hodgkin's disease.

作者信息

Sureda A, Schmitz N

机构信息

Clinical Hematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

出版信息

Ann Oncol. 2002;13 Suppl 1:128-32. doi: 10.1093/annonc/13.s1.128.

Abstract

Little information is available regarding allogeneic stem cell transplantation (alloSCT) and Hodgkin's disease (HD). Autologous stem cell transplantation (autoSCT) is usually preferred to alloSCT due to its widespread availability, lack of the immunological problems intrinsic to the development of graft-versus-host disease (GvHD), and the infrequent bone marrow involvement present in HD patients undergoing high-dose chemotherapy/radiotherapy. AlloSCT has been associated with a high transplant-related mortality (TRM) in patients with HD due to a high incidence of GvHD and of fatal infectious events after transplantation. The poor outcome of these patients after alloSCT may reflect in part the advanced status of the disease at transplantation and the poor performance status of the patient population allografted. Furthermore, the high TRM present in t h e conventional alloSCT setting hasnever allowed a proper evaluation of a possible graft-versus-Hodgkin's effect. In an effort to reduce the TRM associated with alloSCT, low-intensity regimens have been developed; the curative potential of these protocols would rely on the graft-versus-leukemia effect of the allogeneic infusion more than in the conditioning regimen per se. Although the number of HD patients allografted with reduced-intensity protocols is low and the follow-up still short, TRM seems lower than in the conventional allograft setting despite a similar incidence of acute GvHD (aGvHD). Overall and progression-free survival seem promising, and patients developing aGvHD after transplantation or donor lymphocyte infusions seem to be at a lower risk of relapse than those not presenting this complication.

摘要

关于异基因干细胞移植(alloSCT)与霍奇金淋巴瘤(HD)的信息较少。自体干细胞移植(autoSCT)通常比alloSCT更受青睐,这是因为其广泛可得、不存在移植物抗宿主病(GvHD)发生时固有的免疫问题,以及接受大剂量化疗/放疗的HD患者骨髓受累情况不常见。由于GvHD发生率高以及移植后致命感染事件发生率高,alloSCT与HD患者较高的移植相关死亡率(TRM)相关。这些患者在alloSCT后的不良结局可能部分反映了移植时疾病的晚期状态以及接受同种异体移植的患者群体较差的身体状况。此外,传统alloSCT环境中存在的高TRM从未允许对可能的移植物抗霍奇金效应进行适当评估。为了降低与alloSCT相关的TRM,已开发出低强度方案;这些方案的治愈潜力将更多地依赖于异基因输注的移植物抗白血病效应,而非预处理方案本身。尽管采用降低强度方案进行同种异体移植的HD患者数量较少且随访时间仍较短,但尽管急性GvHD(aGvHD)发生率相似,TRM似乎低于传统同种异体移植环境。总体生存率和无进展生存率似乎很有前景,移植后发生aGvHD或接受供体淋巴细胞输注的患者复发风险似乎低于未出现这种并发症的患者。

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