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造血干细胞移植治疗复发或难治性间变大细胞淋巴瘤:日本儿童和青少年的研究。

Haematopoietic stem cell transplantation for relapsed or refractory anaplastic large cell lymphoma: a study of children and adolescents in Japan.

机构信息

Department of Paediatrics, National Kyushu Cancer Centre, Fukuoka, Japan.

出版信息

Br J Haematol. 2015 Feb;168(4):557-63. doi: 10.1111/bjh.13167. Epub 2014 Oct 14.

DOI:10.1111/bjh.13167
PMID:25312752
Abstract

To evaluate haematopoietic stem cell transplantation (HSCT) in children and adolescents, we reviewed the records of 47 patients who were ≤18 years, had relapsed or refractory anaplastic large cell lymphoma, and received HSCT between 1990 and 2010. At HSCT, complete remission (CR) was less common in allogeneic HSCT recipients (n = 24) than in autologous HSCT recipients (n = 23) (P = 0·01). The autologous and allogeneic HSCT groups differed in terms of 5-year event-free survival (EFS) (38% vs. 50%, P = 0·63), cumulative incidence of progress or relapse (49% vs. 28%, P = 0·25), and treatment-related mortality (12% vs. 25%, P = 0·40). However, these differences were not significant. Patients with non-CR at autologous HSCT had a significantly lower EFS rate (14% vs. 48%, P = 0·03). Conversely, although those with non-CR at allogeneic HSCT had a lower EFS rate, this was not significant (44% vs. 63%, P = 0·26). Reduced-intensity conditioning regimens were used for three of the 16 allogeneic HSCTs received by patients with non-CR. These three patients achieved CR, surviving 32-65 months after HSCT. These results demonstrated that allogeneic HSCT might be a treatment option for patients who do not achieve CR through conventional chemotherapy.

摘要

为了评估儿童和青少年造血干细胞移植(HSCT)的效果,我们回顾了 1990 年至 2010 年间接受 HSCT 的 47 例≤18 岁、复发或难治性间变大细胞淋巴瘤患者的记录。在 HSCT 时,异体 HSCT 受者(n=24)完全缓解(CR)的比例明显低于自体 HSCT 受者(n=23)(P=0·01)。自体和异体 HSCT 两组在 5 年无事件生存率(EFS)(38%比 50%,P=0·63)、进展或复发累积发生率(49%比 28%,P=0·25)和治疗相关死亡率(12%比 25%,P=0·40)方面存在差异,但无统计学意义。自体 HSCT 时未达 CR 的患者 EFS 率显著降低(14%比 48%,P=0·03)。相反,虽然异体 HSCT 时未达 CR 的患者 EFS 率较低,但无统计学意义(44%比 63%,P=0·26)。3 例未达 CR 的异体 HSCT 患者接受了强度降低的预处理方案,这 3 例患者均达到 CR,HSCT 后生存 32-65 个月。这些结果表明,对于未通过常规化疗达到 CR 的患者,异体 HSCT 可能是一种治疗选择。

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