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双脐血干细胞移植联合减低强度预处理方案和西罗莫司为基础的移植物抗宿主病预防方案。

Double umbilical cord blood transplantation with reduced intensity conditioning and sirolimus-based GVHD prophylaxis.

机构信息

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

出版信息

Bone Marrow Transplant. 2011 May;46(5):659-67. doi: 10.1038/bmt.2010.192. Epub 2010 Aug 9.

Abstract

The main limitations to umbilical cord blood (UCB) transplantation (UCBT) in adults are delayed engraftment, poor immunological reconstitution and high rates of non-relapse mortality (NRM). Double UCBT (DUCBT) has been used to circumvent the issue of low cell dose, but acute GVHD remains a significant problem. We describe our experience in 32 subjects, who underwent DUCBT after reduced-intensity conditioning with fludarabine/melphalan/antithymocyte globulin and who received sirolimus and tacrolimus to prevent acute GVHD. Engraftment of neutrophils occurred in all patients at a median of 21 days, and platelet engraftment occurred at a median of 42 days. Three subjects had grade II-IV acute GVHD (9.4%) and chronic GVHD occurred in four subjects (cumulative incidence 12.5%). No deaths were caused by GVHD and NRM at 100 days was 12.5%. At 2 years, NRM, PFS and OS were 34.4, 31.2 and 53.1%, respectively. As expected, immunologic reconstitution was slow, but PFS and OS were associated with reconstitution of CD4(+) and CD8(+) lymphocyte subsets, suggesting that recovery of adaptive immunity is required for the prevention of infection and relapse after transplantation. In summary, sirolimus and tacrolimus provide excellent GVHD prophylaxis in DUCBT, and this regimen is associated with low NRM after DUCBT.

摘要

脐带血(UCB)移植(UCBT)在成人中的主要限制是植入延迟、免疫重建不良和非复发死亡率(NRM)高。双份脐带血(DUCBT)已被用于规避细胞剂量低的问题,但急性移植物抗宿主病(GVHD)仍然是一个重大问题。我们描述了 32 名接受氟达拉滨/马法兰/抗胸腺细胞球蛋白低强度预处理后进行 DUCBT 的患者的经验,他们接受西罗莫司和他克莫司预防急性 GVHD。所有患者的中性粒细胞植入中位数为 21 天,血小板植入中位数为 42 天。3 名患者发生 II-IV 级急性 GVHD(9.4%),4 名患者发生慢性 GVHD(累积发生率 12.5%)。无 GVHD 相关死亡,100 天 NRM 为 12.5%。2 年时,NRM、无进展生存期(PFS)和总生存期(OS)分别为 34.4%、31.2%和 53.1%。正如预期的那样,免疫重建缓慢,但 PFS 和 OS 与 CD4(+)和 CD8(+)淋巴细胞亚群的重建相关,这表明移植后预防感染和复发需要适应性免疫的恢复。总之,西罗莫司和他克莫司在 DUCBT 中提供了极好的 GVHD 预防作用,并且这种方案与 DUCBT 后 NRM 低相关。

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