Department of Cardiology and Angiology, University Hospital Muenster, Münster, Germany.
Transplantation. 2011 May 27;91(10):1159-65. doi: 10.1097/TP.0b013e31821774bd.
Few studies have examined everolimus therapy with calcineurin inhibitor (CNI) withdrawal in maintenance heart transplant patients.
In a prospective, single-arm, single-center study, CNI-treated heart transplant patients were converted to everolimus and were followed up for 24 months. The primary endpoints were kidney function and arterial hypertension at 12 and 24 months after conversion.
Fifty-eight patients were recruited (mean time posttransplant 5.6±3.7 years), 55 of whom (91.7%) had renal impairment. Mean creatinine clearance increased from 43.6±21.1 mL/min to 49.5±21.2 mL/min at month 24 (P=0.02). Median blood pressure increased from 120/80 mm Hg at baseline to 122.5/80 mm Hg (P=0.008 and 0.006 for systolic and diastolic pressure, respectively). Lipid parameters did not change significantly over the 24-month follow-up. Early resolution of most non-renal CNI-related adverse events was sustained. CNI therapy was re-introduced at a mean of 309 days (range, 31-684 days) in eight patients after month 6 due to adverse events (n=13) or withdrawal of consent (n=2). No significant changes in cardiac function parameters were observed.
CNI-free immunosuppression with everolimus is an effective and safe option in selected heart transplant maintenance patients. Most adverse effects under everolimus occurred early after conversion and generally resolved without intervention within a few weeks. Refining selection criteria may reduce the need to re-introduce CNI therapy.
很少有研究探讨过在维持性心脏移植患者中使用雷帕霉素联合钙调磷酸酶抑制剂(CNI)停药的方案。
在一项前瞻性、单臂、单中心研究中,接受 CNI 治疗的心脏移植患者转换为雷帕霉素治疗,并随访 24 个月。主要终点为转换后 12 个月和 24 个月时的肾功能和动脉高血压。
共纳入 58 例患者(移植后平均时间 5.6±3.7 年),其中 55 例(91.7%)存在肾功能损害。血肌酐清除率从转换后 24 个月时的 43.6±21.1 mL/min 增加至 49.5±21.2 mL/min(P=0.02)。中位血压从基线时的 120/80 mmHg 升高至 122.5/80 mmHg(收缩压和舒张压分别为 P=0.008 和 0.006)。血脂参数在 24 个月的随访中没有显著变化。大多数非肾 CNI 相关不良事件在早期得到缓解。8 例患者(13 例)因不良事件或撤回同意(n=2)在第 6 个月后平均 309 天(范围 31-684 天)重新开始 CNI 治疗。未观察到心功能参数的显著变化。
在选择的心脏移植维持患者中,使用雷帕霉素进行无 CNI 免疫抑制是一种有效且安全的选择。大多数雷帕霉素相关的不良反应在转换后早期发生,通常在数周内无需干预即可自行缓解。进一步优化选择标准可能会减少重新引入 CNI 治疗的需求。