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在淋巴瘤的减低强度异基因造血干细胞移植中,将西罗莫司添加到移植物抗宿主病预防方案中:一项多中心随机试验。

The addition of sirolimus to the graft-versus-host disease prophylaxis regimen in reduced intensity allogeneic stem cell transplantation for lymphoma: a multicentre randomized trial.

作者信息

Armand Philippe, Kim Haesook T, Sainvil Marie-Michele, Lange Paulina B, Giardino Angela A, Bachanova Veronika, Devine Steven M, Waller Edmund K, Jagirdar Neera, Herrera Alex F, Cutler Corey, Ho Vincent T, Koreth John, Alyea Edwin P, McAfee Steven L, Soiffer Robert J, Chen Yi-Bin, Antin Joseph H

机构信息

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.

出版信息

Br J Haematol. 2016 Apr;173(1):96-104. doi: 10.1111/bjh.13931. Epub 2016 Jan 5.

Abstract

Inhibition of the mechanistic target of rapamycin (mTOR) pathway has clinical activity in lymphoma. The mTOR inhibitor sirolimus has been used in the prevention and treatment of graft-versus-host disease (GVHD) after allogeneic haematopoietic stem cell transplantation (HSCT). A retrospective study suggested that patients with lymphoma undergoing reduced intensity conditioning (RIC) HSCT who received sirolimus as part of their GVHD prophylaxis regimen had a lower rate of relapse. We therefore performed a multicentre randomized trial comparing tacrolimus, sirolimus and methotrexate to standard regimens in adult patients undergoing RIC HSCT for lymphoma in order to assess the possible benefit of sirolimus on HSCT outcome. 139 patients were randomized. There was no difference overall in 2-year overall survival, progression-free survival, relapse, non-relapse mortality or chronic GVHD. However, the sirolimus-containing arm had a significantly lower incidence of grade II-IV acute GVHD (9% vs. 25%, P = 0·015), which was more marked for unrelated donor grafts. In conclusion, the addition of sirolimus for GVHD prophylaxis in RIC HSCT is associated with no increased overall toxicity and a lower risk of acute GVHD, although it does not improve survival; this regimen is an acceptable option for GVHD prevention in RIC HSCT. This trial is registered at clinicaltrials.gov (NCT00928018).

摘要

抑制雷帕霉素作用机制靶点(mTOR)通路在淋巴瘤治疗中具有临床活性。mTOR抑制剂西罗莫司已用于异基因造血干细胞移植(HSCT)后移植物抗宿主病(GVHD)的预防和治疗。一项回顾性研究表明,接受降低强度预处理(RIC)HSCT的淋巴瘤患者,在其GVHD预防方案中使用西罗莫司,复发率较低。因此,我们进行了一项多中心随机试验,比较他克莫司、西罗莫司和甲氨蝶呤与标准方案对接受RIC HSCT治疗淋巴瘤的成年患者的疗效,以评估西罗莫司对HSCT结果可能带来的益处。139名患者被随机分组。在2年总生存率、无进展生存率、复发率、非复发死亡率或慢性GVHD方面,总体上没有差异。然而,含西罗莫司组的II-IV级急性GVHD发生率显著较低(9%对25%,P = 0·015),在无关供体移植中更为明显。总之,在RIC HSCT中添加西罗莫司进行GVHD预防,虽不能提高生存率,但不会增加总体毒性,且急性GVHD风险较低;该方案是RIC HSCT中预防GVHD的一个可接受选择。本试验已在clinicaltrials.gov注册(NCT00928018)。

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