首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Etanercept, mycophenolate, denileukin, or pentostatin plus corticosteroids for acute graft-versus-host disease: a randomized phase 2 trial from the Blood and Marrow Transplant Clinical Trials Network.
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Etanercept, mycophenolate, denileukin, or pentostatin plus corticosteroids for acute graft-versus-host disease: a randomized phase 2 trial from the Blood and Marrow Transplant Clinical Trials Network.

机译:Etanercept,霉酚酸酯,denileukin或pentostatin加上皮质类固醇用于急性移植物抗宿主病:来自血液和骨髓移植临床试验网络的随机2期试验。

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摘要

Acute graft-versus-host disease (aGVHD) is the primary limitation of allogeneic hematopoietic cell transplantation. Corticosteroids remain the standard initial therapy, yet only 25% to 41% of patients completely respond. This randomized, 4-arm, phase 2 trial was designed to identify the most promising agent(s) for initial therapy for aGVHD. Patients were randomized to receive methylprednisolone 2 mg/kg per day plus etanercept, mycophenolate mofetil (MMF), denileukin diftitox (denileukin), or pentostatin. Patients (n = 180) were randomized; their median age was 50 years (range, 7.5-70 years). Myeloablative conditioning represented 66% of transplants. Grafts were peripheral blood (61%), bone marrow (25%), or umbilical cord blood (14%); 53% were from unrelated donors. Patients who received MMF for prophylaxis (24%) were randomized to a non-MMF arm. At randomization, aGVHD was grade I to II (68%), III to IV (32%), and (53%) had visceral organ involvement. Day 28 complete response rates were etanercept 26%, MMF 60%, denileukin 53%, and pentostatin 38%. Corresponding 9-month overall survival was 47%, 64%, 49%, and 47%, respectively. Cumulative incidences of severe infections were as follows: etanercept 48%, MMF 44%, denileukin 62%, and pentostatin 57%. Efficacy and toxicity data suggest the use of MMF plus corticosteroids is the most promising regimen to compare against corticosteroids alone in a definitive phase 3 trial. This study is registered at http://www.clinicaltrials.gov as NCT00224874.
机译:急性移植物抗宿主病(aGVHD)是同种异体造血细胞移植的主要局限性。皮质类固醇仍然是标准的初始治疗方法,但只有25%至41%的患者完全缓解。该随机4臂2期临床试验旨在确定用于aGVHD初始治疗的最有希望的药物。患者被随机接受每天接受2 mg / kg甲基泼尼松龙加依那西普,霉酚酸酯(MMF),denileukin diftitox(denileukin)或喷司他丁。患者(n = 180)被随机分组​​;他们的中位年龄为50岁(范围为7.5-70岁)。清髓条件占移植的66%。移植物为外周血(61%),骨髓(25%)或脐带血(14%); 53%来自无关的捐助者。接受MMF预防的患者(24%)被随机分配到非MMF组。随机分组时,aGVHD为I至II级(68%),III至IV级(32%)和(53%)内脏器官受累。第28天的完全缓解率是依那西普26%,MMF 60%,denileukin 53%和喷司他丁38%。相应的9个月总生存率分别为47%,64%,49%和47%。严重感染的累积发生率如下:依那西普48%,MMF 44%,denileukin 62%和pentostatin 57%。功效和毒性数据表明,在确定的3期试验中,使用MMF加皮质类固醇是与单独使用皮质类固醇进行比较的最有希望的方案。该研究在http://www.clinicaltrials.gov上注册为NCT00224874。

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