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成人T细胞白血病/淋巴瘤的异基因干细胞移植

Allogeneic stem cell transplantation for adult T-cell leukemia/lymphoma.

作者信息

Okamura Jun, Uike Naokuni, Utsunomiya Atae, Tanosaki Ryuji

机构信息

Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka, Japan.

出版信息

Int J Hematol. 2007 Aug;86(2):118-25. doi: 10.1532/IJH97.07070.

Abstract

Adult T-cell leukemia/lymphoma (ATLL) develops in elderly individuals who have been infected with human T-cell leukemia virus type 1 (HTLV-1), and the prognosis for patients with ATLL has been extremely poor. Retrospective studies of allogeneic stem cell transplantation (alloSCT) for selected populations of patients have achieved several encouraging results; however, the reported incidence of transplantation-related mortality (TRM) have been high, even though more than 80% of patients received stem cells from related donors and the patients were relatively young for ATLL. This report documents a prospective feasibility study of alloSCT with reduced-intensity conditioning (RIST) for elderly ATLL patients (>50 years). Regimen-related toxicities and nonhematologic toxicities were acceptable. Fourteen of 15 evaluable patients achieved complete donor chimerism within 90 days, and 1 patient had early TRM after RIST. The HTLV-1 proviral load became undetectable in 8 of 15 patients, suggesting that RIST has potential as an antiviral treatment. The results of alloSCT are promising, and 30% to 40% of patients who achieve remission and have suitable donors can now become long-term survivors with either conventional alloSCT or RIST. It is clear that a graft-versus-ATLL effect is present after alloSCT, regardless of the conditioning regimen or the stem cell source.

摘要

成人T细胞白血病/淋巴瘤(ATLL)发生于感染了1型人类T细胞白血病病毒(HTLV-1)的老年个体中,且ATLL患者的预后一直极差。针对特定患者群体进行异基因干细胞移植(alloSCT)的回顾性研究已取得了一些令人鼓舞的结果;然而,尽管超过80%的患者接受了来自相关供者的干细胞且这些患者相对于ATLL患者而言较为年轻,但报告的移植相关死亡率(TRM)一直很高。本报告记录了一项针对老年ATLL患者(>50岁)采用减低强度预处理(RIST)进行alloSCT的前瞻性可行性研究。方案相关毒性和非血液学毒性均可接受。15例可评估患者中有14例在90天内实现了完全供者嵌合,1例患者在RIST后出现早期TRM。15例患者中有8例的HTLV-1前病毒载量变得无法检测,这表明RIST具有作为抗病毒治疗的潜力。alloSCT的结果很有前景,现在,30%至40%实现缓解且有合适供者的患者通过传统alloSCT或RIST都可成为长期存活者。很明显,无论预处理方案或干细胞来源如何,alloSCT后均存在移植物抗ATLL效应。

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