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他克莫司联合 MTX 或西罗莫司预防移植物抗宿主病的异基因造血干细胞移植受者发生血栓性微血管病的危险因素。

Risk factors for thrombotic microangiopathy in allogeneic hematopoietic stem cell recipients receiving GVHD prophylaxis with tacrolimus plus MTX or sirolimus.

机构信息

1] Department of Hematology, Hospital Universitario de Salamanca, Instituto de Investigación Biomédica de Salamanca (IBSAL), Salamanca, Spain [2] Centro de Investigación del Cáncer, IBMC/CSIC-USAL, Salamanca, Spain.

Department of Hematology, Hospital Universitario de Salamanca, Instituto de Investigación Biomédica de Salamanca (IBSAL), Salamanca, Spain.

出版信息

Bone Marrow Transplant. 2014 May;49(5):684-90. doi: 10.1038/bmt.2014.17. Epub 2014 Feb 24.

DOI:10.1038/bmt.2014.17
PMID:24566710
Abstract

Transplantation-associated thrombotic microangiopathy (TA-TMA) is a feared complication of allogeneic hematopoietic SCT (HSCT) owing to its high mortality rate. The use of calcineurin inhibitors or sirolimus (SIR) for GVHD prophylaxis has been suggested as a potential risk factor. However, the impact of tacrolimus (TAC) and SIR combinations on the increased risk of TA-TMA is currently not well defined. We retrospectively analyzed the incidence of TA-TMA in 102 allogeneic HSCT recipients who consecutively received TAC plus SIR (TAC/SIR) (n=68) or plus MTX (TAC/MTX)±ATG (n=34) for GVHD prophylaxis. No significant differences were observed in the incidence of TA-TMA between patients receiving TAC/SIR vs TAC/MTX±ATG (7.4% vs 8.8%, P=0.8). Only grade III-IV acute GVHD, previous HSCT and serum levels of TAC >25 ng/mL were associated with a greater risk of TA-TMA. Patients developing TA-TMA have significantly poorer survival (P<0.001); however, TA-TMA ceased to be an independent prognostic factor when it was included in a multivariate model. In conclusion, the combination of TAC/SIR does not appear to pose a higher risk of TA-TMA. By contrast, we identified three different risk groups for developing TA-TMA.

摘要

移植相关血栓性微血管病 (TA-TMA) 是异基因造血干细胞移植 (HSCT) 的一种严重并发症,因其死亡率高而备受关注。钙调神经磷酸酶抑制剂或西罗莫司 (SIR) 用于移植物抗宿主病 (GVHD) 预防已被认为是潜在的危险因素。然而,环孢素 (TAC) 和 SIR 联合应用是否会增加 TA-TMA 的风险目前尚不清楚。我们回顾性分析了 102 例连续接受 TAC+SIR (TAC/SIR) (n=68) 或 TAC+MTX±ATG (n=34) 预防 GVHD 的异基因 HSCT 受者中 TA-TMA 的发生率。接受 TAC/SIR 与 TAC/MTX±ATG 的患者 TA-TMA 发生率无显著差异 (7.4% vs 8.8%,P=0.8)。仅 3 级或 4 级急性 GVHD、既往 HSCT 和 TAC 血清水平>25ng/mL 与 TA-TMA 风险增加相关。发生 TA-TMA 的患者生存显著较差 (P<0.001);然而,当将 TA-TMA 纳入多变量模型时,它不再是一个独立的预后因素。总之,TAC/SIR 联合应用似乎不会增加 TA-TMA 的风险。相比之下,我们确定了发生 TA-TMA 的三个不同风险组。

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