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二次异基因造血干细胞移植:治疗移植物失败。

Second allogeneic hematopoietic stem cell transplantation: a treatment for graft failure.

机构信息

Centre for Allogeneic Stem Cell Transplantation, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.

出版信息

Clin Transplant. 2011 Jan-Feb;25(1):E68-76. doi: 10.1111/j.1399-0012.2010.01324.x. Epub 2010 Oct 14.

Abstract

We evaluated the results in 20 recent patients treated with a second hematopoietic stem cell transplantation (HSCT) after graft failure (GF). There were 10 children <18 yr of age. Ten patients had a non-malignant disease, and the other 10 had a malignant disease. In most of the transplantations, fludarabine-based reduced intensity conditioning (RIC) was given. Bone marrow was given to 11 patients, peripheral blood system cell (PBSC) in seven and cord blood to two patients. For the second transplantation (n = 20), a new donor was used in nine cases, while the initial donor was used in 11 transplants. Eight patients (40%) suffered from a second GF. Five of these patients were treated with a third HSCT. The probability of survival was 65% one yr and 60% three yr after the second HSCT. No difference in survival was found between patients transplanted with a new donor (56%) compared to those using the original donor (64%). The three-yr survival was 70% for children compared to 50% for adults (p = ns). Patients with a non-malignant disorder showed a three-yr survival of 90% compared to 20% in patients with a malignant disease (p = 0.005). We concluded that re-transplantation using RIC is a valid option for GF, especially in patients with non-malignant disorders.

摘要

我们评估了 20 例因移植物失败(GF)而接受第二次造血干细胞移植(HSCT)的近期患者的结果。其中有 10 例年龄<18 岁。10 例患者患有非恶性疾病,其余 10 例患有恶性疾病。在大多数移植中,给予基于氟达拉滨的减低强度预处理(RIC)。11 例患者给予骨髓,7 例患者给予外周血系统细胞(PBSC),2 例患者给予脐带血。对于第二次移植(n=20),在 9 例中使用了新供体,而在 11 例移植中使用了初始供体。8 例(40%)患者发生第二次 GF。其中 5 例患者接受了第三次 HSCT 治疗。第二次 HSCT 后 1 年和 3 年的生存率分别为 65%和 60%。使用新供体(56%)与使用原始供体(64%)的患者在生存率方面没有差异。儿童的 3 年生存率为 70%,而成年人的生存率为 50%(p=ns)。与患有恶性疾病的患者(20%)相比,患有非恶性疾病的患者 3 年生存率为 90%(p=0.005)。我们得出结论,使用 RIC 的再移植是 GF 的有效选择,尤其是在患有非恶性疾病的患者中。

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