Hardinger Karen L, Bohl Daniel L, Schnitzler Mark A, Lockwood Mark, Storch Gregory A, Brennan Daniel C
The Department of Pharmacy Practice, University of Missouri-Kansas City, Kansas City, Missouri, USA.
Transplantation. 2005 Jul 15;80(1):41-6. doi: 10.1097/01.tp.0000162980.68628.5a.
To date, the clinical trials of tacrolimus (TAC) versus cyclosporine modified (CsA), have not defined which agent is more cost-effective for immunosuppression in renal transplant recipients especially in a quadruple immunosuppressive regimen.
The objective of this randomized, prospective study was to compare the clinical and economic outcomes of TAC versus CsA, in a regimen that consisted of Thymoglobulin induction, an antimetabolite, and prednisone. Between December 2000 and October 2002, 200 patients were enrolled and randomized in a 2:1 fashion (TAC n=134, CsA n=66).
At 1 year, acute rejection (4% TAC vs. 6% CsA), patient survival (TAC 99% vs. CsA 100%), and graft survival (95% TAC versus 100% CsA, P=0.059) were similar. Serum creatinine levels were lower in the TAC group compared with the CsA group (1.3+/-0.3 vs. 1.6+/-0.7 mg/dL, P=0.03). The incidence of CMV infection was similar between the groups and two patients, both in the TAC arm, developed malignancy. Anti-hypertensive requirement (32% TAC vs. 32% CsA) and the incidence of posttransplant diabetes mellitus (4% TAC vs. 2% CsA) were similar. Pretransplant, fewer TAC patients received dyslipidemia treatment (40% TAC vs. 67% CsA, P=0.0005), while more CsA patients were able to discontinue these medications posttransplant (absolute change 25% TAC vs. 47% CsA). Total 12-month medication costs were similar (17,723 +/- 11,647 dollars TAC vs. 16,515 +/- 10,189 dollars CsA).
When combined with Thymoglobulin induction, an antimetabolite, and corticosteroids, TAC and CsA are comparable in safety, efficacy, and cost in renal transplantation.
迄今为止,他克莫司(TAC)与环孢素(CsA)用于肾移植受者免疫抑制治疗的临床试验,尚未明确哪种药物在四联免疫抑制方案中更具成本效益。
本随机前瞻性研究的目的是比较TAC与CsA在由抗胸腺细胞球蛋白诱导、一种抗代谢药物和泼尼松组成的方案中的临床和经济结局。2000年12月至2002年10月期间,招募了200例患者,并以2:1的比例随机分组(TAC组n = 134,CsA组n = 66)。
1年时,急性排斥反应(TAC组4% vs. CsA组6%)、患者生存率(TAC组99% vs. CsA组100%)和移植物生存率(TAC组95% vs. CsA组100%,P = 0.059)相似。TAC组血清肌酐水平低于CsA组(1.3±0.3 vs. 1.6±0.7 mg/dL,P = 0.03)。两组间巨细胞病毒感染发生率相似,TAC组有两名患者发生恶性肿瘤。抗高血压药物需求率(TAC组32% vs. CsA组32%)和移植后糖尿病发生率(TAC组4% vs. CsA组2%)相似。移植前,接受血脂异常治疗的TAC组患者较少(TAC组40% vs. CsA组67%,P = 0.0005),而更多CsA组患者移植后能够停用这些药物(TAC组绝对变化25% vs. CsA组47%)。12个月的总药物成本相似(TAC组17,723±11,647美元 vs. CsA组16,515±10,189美元)。
当与抗胸腺细胞球蛋白诱导、一种抗代谢药物和皮质类固醇联合使用时,TAC和CsA在肾移植中的安全性、疗效和成本相当。