Comparison of a Tacrolimus/Sirolimus/Prednisone Regimen Versus Tacrolimus/Azathioprine/Prednisone Immunosuppressive Regimen in Lung Transplantation
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 181
- 试验地点
- 1
- 主要终点
- Acute Rejection Rate at 12 Months
研究概览
简要总结
The purpose of this study is to compare the safety and effectiveness of two different anti-rejection drug regimens.
详细描述
This multicenter prospective, randomized controlled clinical trial compared the open label use of sirolimus with that of azathioprine in a tacrolimus-based immunosuppression regimen. Eligible patients were identified during a 90-day screening period immediately after transplantation and randomized via a computer-generated scheme. Patient randomization was stratified according to center and rejection status in the first 90 days after transplantation. All patients received IL-2 receptor antagonist induction therapy, tacrolimus, azathioprine, and corticosteroids until 90 days after transplantation. At 90 days after transplantation, patients were randomized at a 1:1 ratio to either continue azathioprine or change from azathioprine to sirolimus.
The dosing and levels of immunosuppressive medications were standardized for all patients included in this study. Tacrolimus was dosed at 0.04 mg/kg twice daily with target trough levels between 5 and 15 ng/ml, azathioprine was administered at 2 mg/kg daily with dose adjustments for leukopenia, sirolimus was initially dosed at 2 mg/day with target trough levels between 5 and 15 ng/ml, and prednisone was tapered to not more than 10 mg/day by 3 months after transplantation. All patients received induction therapy with either daclizumab or basiliximab as per the product package insert.
In addition, prophylactic antimicrobials were standardized among the participating sites. All patients with either donor and/or recipient cytomegalovirus (CMV)-positive serostatus received either intravenous ganciclovir or oral valganciclovir for a total of 90 days. Lung transplant recipients who were negative for both donor and recipient CMV serostatus received valacyclovir for 90 days. Antifungal prophylaxis was determined by each site. Pneumocystis jiroveci prophylaxis was continued throughout the study. Lipid-lowering medications were recommended according to the National Cholesterol Education Program guidelines.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Lung transplant recipients between the age of 18 and 65 years of age.
- •Females who are capable of becoming pregnant must have a negative pregnancy test prior to consent. (Females of childbearing potential must be using a medically acceptable method of birth control for the duration of the study.)
- •All patients must be able to give written informed consent.
排除标准
- •White blood cell count (WBC) < 4.0/mm3
- •Platelet count < 100,000/mm3
- •Severe hypercholesterolemia (> 350 mg/dl) or hypertriglyceridemia (> 500 mg/dl)
- •Uncontrolled systemic infection at the time of consent.
- •Previous organ transplant
- •Treatment with a drug within the last 30 days that has not received regulatory approval at the time of study entry or for the duration of the study (3 years).
- •Use of maintenance immunosuppression other than daclizumab, tacrolimus, azathioprine, or prednisone prior to randomization.
研究组 & 干预措施
Azathioprine
(tacrolimus,azathioprine/prednisone)
干预措施: azathioprine (Drug)
Sirolimus
tacrolimus/sirolimus/prednisone
干预措施: sirolimus (Drug)
结局指标
主要结局
Acute Rejection Rate at 12 Months
时间窗: 12mos
Raw proportion of patients that experienced acute rejection at or before 12 months.
次要结局
- Severity of Acute Rejection at 12 Months(12 mos)
- Bronchiolitis Obliterans Syndrome (BOS) at 24 Months(24 mos)
- Overall Survival at 36 Months(36 mos)
- Overall Survival at 12 Months(12 mos)
- Overall Survival at 24 Months(24 mos)
- Acute Rejection-free Survival at 12 Months(12 mos)
- Bronchiolitis Obliterans Syndrome (BOS) at 36 Months(36 mos)