Hachem Ramsey R, Yusen Roger D, Chakinala Murali M, Meyers Bryan F, Lynch John P, Aloush Aviva A, Patterson G Alexander, Trulock Elbert P
Division of Pulmonary & Critical Care, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Heart Lung Transplant. 2007 Oct;26(10):1012-8. doi: 10.1016/j.healun.2007.07.027.
The optimal maintenance immunosuppressive regimen after lung transplantation is uncertain.
We conducted a randomized controlled trial of tacrolimus versus cyclosporine in combination with azathioprine and prednisone after lung transplantation. Ninety adults were randomized to tacrolimus (n = 44) or cyclosporine (n = 46). The primary end point was a composite of a cumulative acute rejection A score of 3 or higher, a cumulative lymphocytic bronchitis B score of 4 or higher, or the onset of bronchiolitis obliterans syndrome (BOS) stage 0-p.
Recipients randomized to cyclosporine were significantly more likely to develop the primary end point than those randomized to tacrolimus. During the study period, the primary end point developed in 39 of 46 cyclosporine subjects compared with 24 of 44 tacrolimus subjects (p = 0.002); acute rejection or lymphocytic bronchitis end points developed in 29 of 46 cyclosporine subjects compared with 18 of 44 tacrolimus subjects (p = 0.036). Furthermore, BOS stage 0-p was more likely to develop in the cyclosporine group than in the tacrolimus group, but this was not statistically significant (log-rank p = 0.1). In addition, there was a trend to a higher incidence of diabetes among those in the tacrolimus group, but there was no significant difference in graft survival or the total number of infections, or in the incidence of hypertension, chronic kidney disease, or cancer between the 2 groups.
Tacrolimus is associated with a lower burden of acute rejection and lymphocytic bronchitis and a trend to a greater freedom from BOS stage 0-p than cyclosporine after lung transplantation.
肺移植术后最佳的维持免疫抑制方案尚不确定。
我们进行了一项随机对照试验,比较肺移植术后他克莫司与环孢素联合硫唑嘌呤和泼尼松的效果。90名成年人被随机分为他克莫司组(n = 44)或环孢素组(n = 46)。主要终点是累积急性排斥反应A评分为3或更高、累积淋巴细胞性支气管炎B评分为4或更高,或闭塞性细支气管炎综合征(BOS)0 - p期的发生。
随机分配到环孢素组的受者比随机分配到他克莫司组的受者更有可能出现主要终点。在研究期间,46名环孢素组受试者中有39人出现主要终点,而44名他克莫司组受试者中有24人出现主要终点(p = 0.002);46名环孢素组受试者中有29人出现急性排斥或淋巴细胞性支气管炎终点,而44名他克莫司组受试者中有18人出现(p = 0.036)。此外,环孢素组比他克莫司组更有可能出现BOS 0 - p期,但差异无统计学意义(对数秩检验p = 0.1)。此外,他克莫司组糖尿病发病率有升高趋势,但两组在移植物存活率、感染总数、高血压、慢性肾脏病或癌症发病率方面无显著差异。
与环孢素相比,肺移植术后他克莫司与较低的急性排斥和淋巴细胞性支气管炎负担相关,且有更大可能免于出现BOS 0 - p期。