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首页> 外文期刊>Journal of Clinical Oncology >Multi-institutional study of post-transplantation cyclophosphamide as single-agent graft-versus-host disease prophylaxis after allogeneic bone marrow transplantation using myeloablative busulfan and fludarabine conditioning
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Multi-institutional study of post-transplantation cyclophosphamide as single-agent graft-versus-host disease prophylaxis after allogeneic bone marrow transplantation using myeloablative busulfan and fludarabine conditioning

机译:异基因白消安和氟达拉滨调理异基因骨髓移植后环磷酰胺作为单药移植抗宿主病预防的多机构研究

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Purpose: The clinical safety and efficacy of intravenous busulfan and fludarabine (IV Bu/Flu) myeloablative conditioning as well as graft-versus-host disease (GVHD) prophylaxis with high-dose, posttransplantation cyclophosphamide (PTCy) have been demonstrated independently in several singleinstitutional studies. We hypothesized that combining these two promising approaches in a multiinstitutional study of human leukocyte antigen (HLA)-matched bone marrow transplantation would provide low rates of severe acute and chronic GVHD, low toxicity, and effective disease control.Patients and Methods: Ninety-two adult patients (median age, 49 years; range, 21 to 65 years) with high-risk hematologic malignancies were enrolled at three centers (clinical trial No. NCT00809276). Forty-five patients received related allografts, and 47 received unrelated allografts. GVHD prophylaxis was solely with PTCy at 50 mg/kg/day on post-transplantation days +3 and +4.Results: The cumulative incidences of grades 2 to 4 acute, grades 3 to 4 acute, and chronic GVHD were 51%, 15%, and 14%, respectively. Nonrelapse mortality (NRM) at 100 days and 1 year were 9% and 16%, respectively. With a median follow-up period of 2.2 years, the 2-year disease-free survival (DFS) and overall survival (OS) rates were 62% and 67%, respectively. Donor relatedness did not affect NRM, DFS, or OS. Patients in complete remission (CR) without evidence of minimal residual disease (MRD) had markedly better DFS (80%) and OS (80%) than patients in CR with MRD or with active disease at the time of transplantation (DFS, P =.0005; OS, P =.019).Conclusion: This multi-institutional study demonstrates that PTCy can be safely and effectively combined with IV Bu/Flu myeloablative conditioning and confirms PTCy's efficacy as single-agent, short-course GVHD prophylaxis for both acute and chronic GVHD after bone marrow transplantation from HLA-matched donors.
机译:目的:已在几家单一机构中独立证明了静脉使用白消安和氟达拉滨(IV Bu / Flu)清髓性调理以及高剂量,移植后环磷酰胺(PTCy)预防移植物抗宿主病(GVHD)的临床安全性和有效性学习。我们假设在人类白细胞抗原(HLA)匹配的骨髓移植的多机构研究中结合这两种有前途的方法将提供低的严重急性和慢性GVHD率,低毒性和有效的疾病控制。患者和方法:92在三个中心对患有高危血液恶性肿瘤的成年患者(中位年龄为49岁;范围为21至65岁)进行了研究(临床试验号NCT00809276)。四十五名患者接受了相关的同种异体移植,四十七名患者接受了不相关的同种异体移植。在移植后第3天和+4天,单独使用PTCy预防GVHD的剂量为50 mg / kg /天。结果:2至4级急性,3至4级急性和慢性GVHD的累积发生率分别为51%,15 %和14%。 100天和1年的非复发死亡率(NRM)分别为9%和16%。中位随访期为2.2年,其2年无病生存率(DFS)和总生存率(OS)分别为62%和67%。捐助者相关性不影响NRM,DFS或OS。完全缓解(CR)但无最小残留病(MRD)证据的患者,其DFS(80%)和OS(80%)明显优于移植时有MRD或活动性疾病的CR患者(DFS,P =结论:这项多机构研究表明,PTCy可以安全有效地与IV Bu / Flu清髓性调理相结合,并证实PTCy作为单药,短程GVHD预防两者的功效。 HLA匹配供体骨髓移植后的急性和慢性GVHD。

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