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