Falck Pål, Vethe Nils Tore, Asberg Anders, Midtvedt Karsten, Bergan Stein, Reubsaet Jan Leo Egge, Holdaas Hallvard
Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, PO Box 1068 Blindern, 0316 Oslo, Norway.
Nephrol Dial Transplant. 2008 Mar;23(3):1048-53. doi: 10.1093/ndt/gfm632. Epub 2007 Oct 23.
The calcimimetic drug cinacalcet offers a novel therapeutic option to treat post-transplant hypercalcemia and hyperparathyroidism; however, the interaction with calcineurin inhibitors and mycophenolate has not been evaluated.
In the present study the effects of cinacalcet on the pharmacokinetics of cyclosporine A (CsA), tacrolimus (Tac) and mycophenolate were investigated in 14 renal transplant recipients with stable renal function (mean creatinine 126.4 +/- 45.3 micromol/L). The patients were treated with either CsA (n = 8) or Tac (n = 6) in combination with mycophenolate/azathioprine and steroids. Twelve-hour pharmacokinetic investigations to measure CsA and its six main metabolites, Tac and mycophenolate concentrations were performed before and after 1-week treatment with 30 mg cinacalcet once daily.
Cinacalcet treatment induced a significant 14.3 +/- 12.1% decrease in Tac AUC(0-12) (P = 0.039). Tac C(max), T(max) and T(1/2) also tended to decrease. The pharmacokinetics of CsA and mycophenolate were not significantly affected by concomitant treatment with cinacalcet. However, the secondary CsA metabolite, AM19, showed a significant increase of 9.0 +/- 9.5% during cinacalcet treatment (P = 0.040). Renal function decreased significantly from 78 +/- 11 to 72 +/- 12 mL/min (P = 0.019) and correlated with the increased levels of metabolite AM19 in the CsA group. Renal function was unchanged in the Tac group.
Cinacalcet treatment showed a moderate effect on the Tac, but not CsA or mycophenolate, pharmacokinetics after 1-week concomitant treatment. This interaction appears to have minor clinical relevance. However, it is advisable to monitor renal function in CsA-treated patients due to the observed decrease in renal function.
拟钙剂西那卡塞为治疗移植后高钙血症和甲状旁腺功能亢进提供了一种新的治疗选择;然而,其与钙调神经磷酸酶抑制剂和霉酚酸酯的相互作用尚未得到评估。
在本研究中,对14例肾功能稳定(平均肌酐126.4±45.3微摩尔/升)的肾移植受者,研究了西那卡塞对环孢素A(CsA)、他克莫司(Tac)和霉酚酸酯药代动力学的影响。患者接受CsA(n = 8)或Tac(n = 6)联合霉酚酸酯/硫唑嘌呤和类固醇治疗。在每日一次给予30毫克西那卡塞治疗1周前后,进行12小时药代动力学研究,以测量CsA及其六种主要代谢物、Tac和霉酚酸酯的浓度。
西那卡塞治疗使Tac的AUC(0 - 12)显著降低14.3±12.1%(P = 0.039)。Tac的C(max)、T(max)和T(1/2)也有下降趋势。西那卡塞联合治疗对CsA和霉酚酸酯的药代动力学无显著影响。然而,CsA的次要代谢物AM19在西那卡塞治疗期间显著增加了9.0±9.5%(P = 0.040)。CsA组肾功能从78±11显著降至72±12毫升/分钟(P = 0.019),且与代谢物AM19水平升高相关。Tac组肾功能无变化。
西那卡塞治疗1周联合用药后,对Tac的药代动力学有中度影响,但对CsA或霉酚酸酯无影响。这种相互作用似乎临床相关性较小。然而,鉴于观察到的肾功能下降,建议对接受CsA治疗的患者监测肾功能。