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T 细胞耗竭的异基因造血干细胞移植后晚期非霍奇金淋巴瘤患者二线年龄调整国际预后指数。

Second-line age-adjusted International Prognostic Index in patients with advanced non-Hodgkin lymphoma after T-cell depleted allogeneic hematopoietic SCT.

机构信息

Allogeneic Bone Marrow Transplantation Service, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

出版信息

Bone Marrow Transplant. 2010 Sep;45(9):1408-16. doi: 10.1038/bmt.2009.371. Epub 2010 Jan 11.

Abstract

T-cell depleted allogeneic hematopoietic SCT (TCD-HSCT) have shown durable disease-free survival with a low risk of GVHD in patients with AML. We investigated this approach in 61 patients with primary refractory or relapsed non-Hodgkin lymphoma (NHL), who underwent TCD-HSCT from January 1992 through September 2004. Patients received myeloablative cytoreduction consisting of hyperfractionated total body irradiation, followed by either thiotepa and cyclophosphamide (45 patients) or thiotepa and fludarabine (16 patients). We determined the second-line age-adjusted International Prognostic Index score (sAAIPI) before transplant transplant. Median follow-up of surviving patients is 6 years. The 10-year OS and EFS were 50% and 43%, respectively. The relapse rate at 10 years was 21% in patients with chemosensitive disease and 52% in those with resistant disease at time of HSCT. Nine of the 18 patients who relapsed entered a subsequent CR. OS (P=0.01) correlated with the sAAIPI. The incidence of grades II-IV acute GVHD was 18%. We conclude that allogeneic TCD-HSCT can induce high rates of OS and EFS in advanced NHL with a low incidence of GVHD. Furthermore, the sAAIPI can predict outcomes and may be used to select the most appropriate patients for this type of transplant.

摘要

T 细胞耗竭的同种异体造血干细胞移植(TCD-HSCT)在 AML 患者中显示出无疾病存活的持久缓解,GVHD 风险低。我们对 1992 年 1 月至 2004 年 9 月期间接受 TCD-HSCT 的 61 例原发性难治性或复发性非霍奇金淋巴瘤(NHL)患者进行了这项研究。患者接受了包括超分割全身照射在内的大剂量细胞减灭性预处理,然后接受噻替哌和环磷酰胺(45 例)或噻替哌和氟达拉滨(16 例)治疗。我们在移植前确定了二线年龄调整的国际预后指数评分(sAAIPI)。存活患者的中位随访时间为 6 年。10 年 OS 和 EFS 分别为 50%和 43%。在 HSCT 时疾病缓解的患者中,10 年复发率为 21%,耐药患者为 52%。18 例复发患者中有 9 例进入了随后的 CR。OS(P=0.01)与 sAAIPI 相关。II-IV 级急性 GVHD 的发生率为 18%。我们得出结论,同种异体 TCD-HSCT 可在 NHL 晚期诱导高 OS 和 EFS 率,GVHD 发生率低。此外,sAAIPI 可预测结局,并可用于选择最适合此类移植的患者。

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