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异基因干细胞移植能够诱导血管免疫母细胞性T细胞淋巴瘤长期缓解:来自欧洲血液与骨髓移植组淋巴瘤工作组的一项回顾性研究

Allogeneic stem cell transplantation is able to induce long-term remissions in angioimmunoblastic T-cell lymphoma: a retrospective study from the lymphoma working party of the European group for blood and marrow transplantation.

作者信息

Kyriakou Charalampia, Canals Carmen, Finke Jürgen, Kobbe Guido, Harousseau Jean-Luc, Kolb Hans-Jochem, Novitzky Nicolas, Goldstone Anthony H, Sureda Anna, Schmitz Norbert

机构信息

North West London Hospitals National Health Service Trust, Middlesex, UK.

出版信息

J Clin Oncol. 2009 Aug 20;27(24):3951-8. doi: 10.1200/JCO.2008.20.4628. Epub 2009 Jul 20.

DOI:10.1200/JCO.2008.20.4628
PMID:19620487
Abstract

PURPOSE

To analyze the long-term outcome in terms of nonrelapse mortality (NRM), relapse rate (RR), progression-free survival (PFS), and overall survival (OS) in patients with angioimmunoblastic T-cell lymphoma (AITL) treated with allogeneic stem-cell transplantation (alloSCT).

PATIENTS AND METHODS

Forty-five patients with AITL who had undergone an alloSCT between January 1998 and December 2005 and were registered in the European Group for Blood and Marrow Transplantation database were analyzed. Median age was 48 years (range, 23 to 68 years), 34 patients had received > or = two lines of chemotherapy before alloSCT, and 11 patients had experienced treatment failure with a prior autologous stem-cell transplantation. Twenty-five patients underwent a myeloablative alloSCT, and 20 underwent a reduced-intensity alloSCT. Donors were HLA-identical siblings in 26 patients. Twenty-seven patients were allografted in chemotherapy-sensitive disease, and 18 were allografted in refractory disease.

RESULTS

The cumulative incidence of NRM was 18%, 22%, and 25% at 3, 6, and 12 months, respectively. Patients with poor performance status had a significantly higher NRM (P = .01). RR was estimated as 16% and 20% at 2 and 3 years, respectively, and was lower in patients developing chronic graft-versus-host disease (cGVHD). PFS and OS rates were 62% and 53% and 66% and 64% at 1 and 3 years, respectively, and were significantly better in chemotherapy-sensitive patients.

CONCLUSION

AlloSCT represents a valid therapeutic option for patients with AITL. Both the lower RR after transplantation as well as the decreased RR in patients developing cGVHD after the alloSCT suggests the existence of a clinically relevant graft-versus-lymphoma effect.

摘要

目的

分析接受异基因干细胞移植(alloSCT)治疗的血管免疫母细胞性T细胞淋巴瘤(AITL)患者的非复发死亡率(NRM)、复发率(RR)、无进展生存期(PFS)和总生存期(OS)的长期结局。

患者和方法

分析了1998年1月至2005年12月间接受alloSCT并登记在欧洲血液和骨髓移植组数据库中的45例AITL患者。中位年龄为48岁(范围23至68岁),34例患者在alloSCT前接受了≥2线化疗,11例患者先前自体干细胞移植治疗失败。25例患者接受了清髓性alloSCT,20例接受了减低强度的alloSCT。26例患者的供者为HLA相同的同胞。27例患者在化疗敏感疾病时进行了异基因移植,18例在难治性疾病时进行了异基因移植。

结果

NRM的累积发生率在3个月、6个月和12个月时分别为18%、22%和25%。体能状态差的患者NRM显著更高(P = 0.01)。RR在2年和3年时分别估计为16%和20%,在发生慢性移植物抗宿主病(cGVHD)的患者中较低。PFS率和OS率在1年和3年时分别为62%和53%以及66%和64%,化疗敏感患者明显更好。

结论

alloSCT是AITL患者的一种有效治疗选择。移植后较低的RR以及alloSCT后发生cGVHD患者RR的降低提示存在临床相关的移植物抗淋巴瘤效应。

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