Department of Nephrology, Charité University, Berlin, Germany.
Am J Transplant. 2010 Mar;10(3):571-81. doi: 10.1111/j.1600-6143.2009.02980.x. Epub 2010 Jan 29.
Sotrastaurin, a novel protein-kinase-C inhibitor, blocks early T-cell activation. In this 12-month, Phase II study, de novo renal-transplant patients were randomized to sotrastaurin (200 mg b.i.d.) + standard-exposure tacrolimus (SET) or reduced-exposure tacrolimus (RET) (SET: n = 76; RET: n = 66), or control (SET + mycophenolic acid [MPA, 720 mg b.i.d.]; n = 74). In both sotrastaurin groups, patients were converted from tacrolimus to MPA after Month 3, achieving calcineurin inhibitor-free immunosuppression. The primary endpoint was composite efficacy failure (treated biopsy-proven acute rejection, graft loss, death or loss to follow-up). The key secondary endpoint was glomerular filtration rate (GFR). Composite efficacy failure rates were: 4.1%, 5.4% and 1.5% at Month 3 (preconversion) and 7.8%, 44.8% and 34.1% at study end in the control, sotrastaurin + SET and sotrastaurin + RET groups, respectively; these results led to premature study discontinuation. Median GFR at Month 6 was: 57.0, 53.0 and 60.0 mL/min/1.73 m(2), respectively. Study-drug discontinuations due to adverse events occurred in 16.2%, 18.4% and 12.1%, respectively. Leukopenia and neutropenia occurred more frequently preconversion in control versus sotrastaurin groups: 13.7%, 5.6%, and 4.6%; and 11.1%, 4.3% and 3.1%, respectively. The initial sotrastaurin + tacrolimus regimen was efficacious and well tolerated but the postconversion sotrastaurin + MPA regimen showed inadequate efficacy. Longer-term evaluation of sotrastaurin + tacrolimus is warranted.
索他司他汀是一种新型蛋白激酶 C 抑制剂,可阻断 T 细胞早期激活。在这项为期 12 个月的 II 期研究中,初治肾移植患者被随机分为索他司他汀(200mg,每日两次)+标准剂量他克莫司(SET)或低剂量他克莫司(RET)(SET:n=76;RET:n=66),或对照组(SET+麦考酚酸[MPA,720mg,每日两次];n=74)。在索他司他汀两组中,患者在第 3 个月时从他克莫司转换为 MPA,实现了钙调磷酸酶抑制剂的免疫抑制。主要终点是复合疗效失败(治疗性活检证实的急性排斥反应、移植物丢失、死亡或失访)。关键次要终点是肾小球滤过率(GFR)。对照组、索他司他汀+SET 和索他司他汀+RET 组在第 3 个月(转换前)和研究结束时的复合疗效失败率分别为:4.1%、5.4%和 1.5%,7.8%、44.8%和 34.1%;这些结果导致研究提前终止。第 6 个月时的中位 GFR 分别为:57.0、53.0 和 60.0mL/min/1.73m(2)。由于不良事件而导致研究药物停药的分别为:16.2%、18.4%和 12.1%。对照组与索他司他汀组相比,在转换前更频繁地出现白细胞减少和中性粒细胞减少:13.7%、5.6%和 4.6%;11.1%、4.3%和 3.1%。初始索他司他汀+他克莫司方案有效且耐受性良好,但转换后索他司他汀+MPA 方案疗效不足。需要对索他司他汀+他克莫司进行更长期的评估。