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Ruxolitinib in refractory acute and chronic graft-versus-host disease: a multicenter survey study

机译:Ruxolitinib在难治性急性和慢性移植物与宿主疾病中:多中心调查研究

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Graft-versus-host disease is the main cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation. First-line treatment is based on the use of high doses of corticosteroids. Unfortunately, second-line treatment for both acute and chronic graft-versus-host disease, remains a challenge. Ruxolitinib has been shown as an effective and safe treatment option for these patients. Seventy-nine patients received ruxolitinib and were evaluated in this retrospective and multicenter study. Twenty-three patients received ruxolitinib for refractory acute graft-versus-host disease after a median of 3 (range 1-5) previous lines of therapy. Overall response rate was 69.5% (16/23) which was obtained after a median of 2 weeks of treatment, and 21.7% (5/23) reached complete remission. Fifty-six patients were evaluated for refractory chronic graft-versus-host disease. The median number of previous lines of therapy was 3 (range 1-10). Overall response rate was 57.1% (32/56) with 3.5% (2/56) obtaining complete remission after a median of 4 weeks. Tapering of corticosteroids was possible in both acute (17/23, 73%) and chronic graft-versus-host disease (32/56, 57.1%) groups. Overall survival was 47% (CI: 23-67%) at 6 months for patients with aGVHD (62 vs 28% in responders vs non-responders) and 81% (CI: 63-89%) at 1 year for patients with cGVHD (83 vs 76% in responders vs non-responders). Ruxolitinib in the real life setting is an effective and safe treatment option for GVHD, with an ORR of 69.5% and 57.1% for refractory acute and chronic graft-versus-host disease, respectively, in heavily pretreated patients.
机译:移植物与宿主病是同种异体造血干细胞移植后发病率和死亡率的主要原因。一线治疗基于使用高剂量的皮质类固醇。不幸的是,对急性和慢性接枝的二线治疗仍然是一个挑战。 Raxolitinib已被显示为这些患者的有效和安全的治疗选择。七十九个患者接受了罗西替尼,并在这个回顾性和多中心研究中进行了评估。二十三名患者在中位数的中位治疗后,23名患者接受Raxolitinib用于难治性急性移植物 - 与宿主疾病。总体反应率为69.5%(16/23),在治疗2周后获得,21.7%(5/23)达到完全缓解。评估五十六名患者,用于难治性慢性接枝 - 与宿主疾病。先前治疗系数的中值为3(范围1-10)。整体反应率为57.1%(32/56),3.5%(2/56)在4周中中位后获得完全缓解。在急性(17/23,73%)和慢性接枝 - 与宿主疾病(32/56,57.1%)组中,逐渐变细。对于CGVHD患者的1年,总生存率为6个月,在6个月内为6个月(62 vs 28%)和CGVHD患者的81%(CI:63-89%),总存活率为47%(CI:23-67%),患者为81%(CI:63-89%) (响应者83 vs 76%vs非响应者)。 Ruxolitinib在现实生活中是一种有效和安全的GVHD治疗选择,ORR分别为难治性急性和慢性移植术患者的难治性急性和慢性接枝腹膜疾病。

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