Park Sehoon, Kim Yon Su, Lee Jungpyo, Huh Wooseong, Yang Chul Woo, Kim Young-Lim, Kim Yeong Hoon, Kim Joong Kyung, Oh Chang-Kwon, Park Su-Kil
Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
Department of Internal Medicine, Seoul National University Hospital, Seoul, South Korea.
Ann Transplant. 2018 Jun 12;23:401-411. doi: 10.12659/AOT.909036.
BACKGROUND Minimizing the tacrolimus dosage in patients with stable allograft function needs further investigation. MATERIAL AND METHODS We performed an open-label, randomized, controlled study from 2010 to 2016 in 7 tertiary teaching hospitals in Korea and enrolled 345 kidney transplant recipients with a stable graft status. The study group received reduced-dose tacrolimus, 1080-1440 mg/day of enteric-coated mycophenolate sodium (EC-MPS), and corticosteroids. The control group received the standard tacrolimus dosage and 540-720 mg/day of EC-MPS with steroids. The primary endpoint was the mean estimated glomerular filtration rate (eGFR) and change in the eGFR at 12 months after randomization. RESULTS The mean tacrolimus trough level of the study group was 4.51±1.62 ng/mL, which was lower than that of the control group, at 6.75±2.82 ng/mL (P<0.001). The primary endpoint was better in the study group in terms of change in eGFR (P<0.001). The month 12 eGFRs were 73.6±28.4 and 68.3±18.1 mL/min/1.73 m² in the study and the control groups, respectively, but the difference did not reach statistical significance (P=0.07). The incidence of adverse events was similar between the study and the control groups. CONCLUSIONS Minimizing tacrolimus to a trough level below 5 ng/mL combined with conventional EC-MPS can be considered in patients with a steady follow-up, as it was associated with small benefits in the changes of the eGFR (Clinicaltrials.gov number: NCT01159080).
在移植肾功能稳定的患者中尽量减少他克莫司剂量仍需进一步研究。
2010年至2016年,我们在韩国7家三级教学医院开展了一项开放标签、随机对照研究,纳入345例移植肾功能稳定的肾移植受者。研究组接受低剂量他克莫司、1080 - 1440毫克/天的肠溶型霉酚酸钠(EC - MPS)和皮质类固醇。对照组接受标准剂量他克莫司以及540 - 720毫克/天的EC - MPS加类固醇。主要终点是随机分组后12个月时的平均估计肾小球滤过率(eGFR)及其变化。
研究组他克莫司谷浓度均值为4.51±1.62纳克/毫升,低于对照组的6.75±2.82纳克/毫升(P<0.001)。就eGFR变化而言,研究组的主要终点表现更佳(P<0.001)。研究组和对照组在第12个月时的eGFR分别为73.6±28.4和68.3±18.1毫升/分钟/1.73平方米,但差异未达到统计学显著性(P = 0.07)。研究组和对照组不良事件发生率相似。
对于随访稳定的患者,可考虑将他克莫司谷浓度降至5纳克/毫升以下并联合常规EC - MPS,因为这在eGFR变化方面有微小益处(Clinicaltrials.gov编号:NCT01159080)。