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A phase II/III randomized multicenter trial of prednisone/sirolimus versus prednisone/ sirolimus/calcineurin inhibitor for the treatment of chronic graft-versus-host disease: BMT CTN 0801

机译:泼尼松/西罗莫司与泼尼松/西罗莫司/钙调神经磷酸酶抑制剂治疗慢性移植物抗宿主病的II / III期随机多中心试验:BMT CTN 0801

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摘要

Initial therapy of chronic graft-versus-host disease is prednisone ± a calcineurin-inhibitor, but most patients respond inadequately. In a randomized, adaptive, phase II/III, multicenter trial we studied whether prednisone/sirolimus or prednisone/sirolimus/photopheresis was more effective than prednisone/sirolimus/calcineurin-inhibitor for treating chronic graft-versus-host disease in treatment-naïve or early inadequate responders. Primary endpoints of this study were proportions of subjects alive without relapse or secondary therapy with 6-month complete or partial response in phase II, or with 2-year complete response in phase III. The prednisone/sirolimus/photopheresis arm closed prematurely because of slow accrual and the remaining two-drug versus three-drug study ended in phase II due to statistical futility with 138 evaluable subjects. The two-drug and three-drug arms did not differ in rates of 6-month complete or partial response (48.6% versus 50.0%, P=0.87), or 2-year complete response (14.7% versus 15.5%, P=0.90). Serum creatinine values >1.5 times baseline were less frequent in the calcineurin-inhibitor-free arm at 2 months (1.5% versus 11.7%, P=0.025) and 6 months (7.8% versus 24.0%, P=0.016). Higher adjusted Short Form-36 Physical Component Summary and Physical Functioning scores were seen in the two-drug arm at both 2 months (P=0.02 and P=0.04, respectively) and 6 months (P=0.007 and P=0.001, respectively). Failure-free survival and overall survival rates at 2 years were similar for patients in the the two-drug and three-drug arms (48.6% versus 46.2%, P=0.78; 81.5% versus 74%, P=0.28). Based on similar long-term outcomes, prednisone/sirolimus is a therapeutic alternative to prednisone/sirolimus/calcineurin-inhibitor for chronic graft-versus-host disease, being easier to administer and better tolerated. identifier: .
机译:慢性移植物抗宿主病的初始治疗方法是泼尼松(一种钙调神经磷酸酶抑制剂),但大多数患者反应不足。在一项随机,适应性II / III期多中心试验中,我们研究了泼尼松/西罗莫司或泼尼松/西罗莫司/光血疗法比单纯泼尼松/西罗莫司/钙调神经磷酸酶抑制剂治疗初治或初治的慢性移植物抗宿主病更有效早期响应者不足。这项研究的主要终点是II期为6个月的完全或部分缓解或III期为2年的完全缓解而未复发或未接受二次治疗的受试者比例。泼尼松/西罗莫司/光胆疗法手臂过早地关闭,因为其累积缓慢,其余的两药和三药研究由于对138名可评估受试者的统计无效而在第二阶段结束。两药和三药组在6个月的完全或部分缓解率(48.6%对50.0%,P = 0.87)或2年完全缓解率(14.7%对15.5%,P = 0.90)方面没有差异。 )。在无钙调神经磷酸酶抑制剂组中,血清肌酐值>基线值的1.5倍在2个月(1.5%vs. 11.7%,P = 0.025)和6个月(7.8%vs 24.0%,P = 0.016)时较少。在2个月(分别为P = 0.02和P = 0.04)和6个月(分别为P = 0.007和P = 0.001)的两个药物治疗组中,均获得了较高的调整后的简短36型身体成分总结和身体机能评分。 。两药和三药组患者的两年无故障生存率和总生存率相似(48.6%对46.2%, P = 0.78; 81.5% 74%, P = 0.28)。基于相似的长期结果,泼尼松/西罗莫司是治疗慢性移植物抗宿主病的泼尼松/西罗莫司/钙调神经磷酸酶抑制剂,具有更强的治疗和耐受性。 标识符:。

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