全淋巴细胞照射和抗胸腺细胞球蛋白非清髓性治疗后同种异体移植患者移植物抗宿主病的发病率和模式

Bone Marrow Research Pub Date : 2013-01-01 Epub Date: 2013-04-17 DOI:10.1155/2013/414959
Lauren Veltri, Michael Regier, Aaron Cumpston, Sonia Leadmon, William Tse, Michael Craig, Mehdi Hamadani
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引用次数: 11

摘要

非清髓性(NMA)调节与全淋巴照射和抗胸腺细胞球蛋白(TLI/ATG)已被证明可预防急性移植物抗宿主病(GVHD)。在此,我们报告了我们在TLI/ATG治疗NMA后同种异体移植的机构经验(n = 21)。GVHD预防包括钙调磷酸酶抑制剂和霉酚酸酯的组合。患者中位年龄为59岁。存活患者的中位随访时间为545天。1例患者出现原发性移植排斥反应。中性粒细胞移植的中位时间为18天,血小板移植的中位时间为9.5天。第100天II-IV级急性GVHD的累积发病率(CI)为28.6%,第180天为38.1%。III-IV级急性GVHD的CI为28.6%。慢性GVHD患者1年时CI为45.2%。1年时疾病复发的CI为9.5%。第100天非复发死亡率(NRM)为0%,第1年仅为9.5%。1年总生存率和无进展生存率分别为81%和80.4%。我们有限的回顾性数据显示,基于TLI/ atg的NMA调节的复发率和NRM率令人鼓舞,但急性和慢性GVHD的发生率高于之前报道的,这强调了设计有效预防GVHD的新策略的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Incidence and Pattern of Graft-versus-Host Disease in Patients Undergoing Allogeneic Transplantation after Nonmyeloablative Conditioning with Total Lymphoid Irradiation and Antithymocyte Globulin.

Incidence and Pattern of Graft-versus-Host Disease in Patients Undergoing Allogeneic Transplantation after Nonmyeloablative Conditioning with Total Lymphoid Irradiation and Antithymocyte Globulin.

Incidence and Pattern of Graft-versus-Host Disease in Patients Undergoing Allogeneic Transplantation after Nonmyeloablative Conditioning with Total Lymphoid Irradiation and Antithymocyte Globulin.

Incidence and Pattern of Graft-versus-Host Disease in Patients Undergoing Allogeneic Transplantation after Nonmyeloablative Conditioning with Total Lymphoid Irradiation and Antithymocyte Globulin.

Nonmyeloablative (NMA) conditioning with total lymphoid irradiation and antithymocyte globulin (TLI/ATG) has been shown to protect against acute graft-versus-host disease (GVHD). We report here our institutional experience with allogeneic transplantation following NMA conditioning with TLI/ATG (n = 21). GVHD prophylaxis consisted of a combination of a calcineurin inhibitor and mycophenolate mofetil. Median patient age was 59 years. The median followup of surviving patients is 545 days. One patient experienced primary graft rejection. The median time to neutrophil engraftment was 18 days and platelet engraftment was 9.5 days. The cumulative incidence (CI) of grade II-IV acute GVHD at day +100 was 28.6% and 38.1% at day +180. The CI for grade III-IV acute GVHD was 28.6% at day +180. CI of chronic GVHD was 45.2% at 1 year. The CI of disease relapse was 9.5% at 1 year. The rate of nonrelapse mortality (NRM) was 0% at day +100 and only 9.5% at 1 year. The overall and progression free survival at 1 year was 81% and 80.4%, respectively. Our limited, retrospective data show encouraging relapse and NRM rates with TLI/ATG-based NMA conditioning, but with higher than previously reported rates of acute and chronic GVHD, underscoring the need for novel strategies designed to effectively prevent GVHD.

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