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采用他克莫司/西罗莫司预防移植物抗宿主病,联合强度降低的预处理方案进行异基因造血细胞移植治疗骨髓纤维化,可改善预后。

Improved outcomes using tacrolimus/sirolimus for graft-versus-host disease prophylaxis with a reduced-intensity conditioning regimen for allogeneic hematopoietic cell transplant as treatment of myelofibrosis.

机构信息

City of Hope Cancer Center, Department of Hematology/HCT, Duarte, California 91010, USA.

出版信息

Biol Blood Marrow Transplant. 2010 Feb;16(2):281-6. doi: 10.1016/j.bbmt.2009.09.020. Epub 2009 Sep 26.

Abstract

Allogeneic hematopoietic cell transplantation (HCT) using reduced-intensity conditioning (RIC) regimens is a potentially curative treatment for patients (patients) with myelofibrosis (MF), as we and others have reported. Nonrelapse mortality (NRM) from graft-versus-host disease (GVHD) and other complications has limited the success of this approach. As part of an ongoing prospective research study at City of Hope, a combination of tacrolimus/sirolimus +/- methotrexate (MTX) for GVHD prophylaxis has become the standard treatment for our allogeneic HCT patients. In this report, we present results for 23 consecutive patients, including extended follow up for 9 patients previously reported who received cyclosporine (CsA)/mycophenolate moffetil (MMF)+/-MTX, and the current series of 14 patients who received tacrolimus/sirolimus+/-MTX, and evaluate the impact of the GVHD prophylaxis regimen on the outcomes. Median follow-up for alive patients was 29.0 months (9.5-97.0). The estimated 2-year overall survival (OS) for the CsA/MMF cohort was 55.6% (confidence interval 36.0, 71.3), and for the tacrolimus/sirolimus cohort it was 92.9% (63.3, 98.8) (P=.047). The probability of grade III or IV acute GVHD (aGVHD) was 60% for the CsA/MMF patients, and 10% for the tacrolimus/sirolimus group (P=.0102). No significant differences were seen for grade II to IV aGVHD in the 2 groups. We conclude that the combination of tacrolimus/sirolimus+/-MTX for GVHD prophylaxis in the setting of RIC HCT for MF appears to reduce the incidence of severe aGVHD and NRM, and leads to improved OS compared to CSA/MMF+/-MTX.

摘要

异基因造血细胞移植(HCT)使用强度降低的调理(RIC)方案是治疗骨髓纤维化(MF)患者的潜在治愈性治疗方法,正如我们和其他人所报道的那样。移植物抗宿主病(GVHD)和其他并发症导致的非复发死亡率(NRM)限制了这种方法的成功。作为希望之城正在进行的前瞻性研究的一部分,他克莫司/西罗莫司 +/-甲氨蝶呤(MTX)联合用于 GVHD 预防已成为我们异基因 HCT 患者的标准治疗方法。在本报告中,我们报告了 23 例连续患者的结果,其中包括之前接受环孢素(CsA)/霉酚酸酯(MMF)+/-MTX 治疗的 9 例患者的扩展随访,以及当前系列的 14 例接受他克莫司/西罗莫司+/-MTX 治疗的患者,并评估了 GVHD 预防方案对结果的影响。存活患者的中位随访时间为 29.0 个月(9.5-97.0)。CsA/MMF 队列的 2 年总生存率(OS)估计为 55.6%(置信区间 36.0,71.3),而他克莫司/西罗莫司队列为 92.9%(63.3,98.8)(P=.047)。CsA/MMF 患者的 3 级或 4 级急性 GVHD(aGVHD)概率为 60%,而他克莫司/西罗莫司组为 10%(P=.0102)。两组间 2 级至 4 级 aGVHD 无显著差异。我们得出结论,RIC HCT 治疗 MF 时,他克莫司/西罗莫司+/-MTX 联合用于 GVHD 预防似乎可降低严重 aGVHD 和 NRM 的发生率,并导致 OS 改善,优于 CSA/MMF+/-MTX。

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