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Ph 染色体阳性急性淋巴细胞白血病患者接受无关供者脐带血移植。

Umbilical cord blood transplantation from unrelated donors in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia.

出版信息

Haematologica. 2014 Feb;99(2):378-84. doi: 10.3324/haematol.2013.091009. Epub 2013 Oct 4.

DOI:10.3324/haematol.2013.091009
PMID:24097633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3912971/
Abstract

There are very few disease-specific studies focusing on outcomes of umbilical cord blood transplantation for Philadelphia chromosome-positive acute lymphoblastic leukemia. We report the outcome of 45 patients with Philadelphia chromosome-positive acute lymphoblastic leukemia who underwent myeloablative single unit cord blood transplantation from unrelated donors within the GETH/GITMO cooperative group. Conditioning regimens were based on combinations of thiotepa, busulfan, cyclophospamide or fludarabine, and antithymocyte globulin. At the time of transplantation, 35 patients (78%) were in first complete remission, four (8%) in second complete remission and six (14%) in third or subsequent response. The cumulative incidence of myeloid engraftment was 96% at a median time of 20 days and significantly better for patients receiving higher doses of CD34(+) cells. The incidence of acute grade II-IV graft-versus-host disease was 31%, while that of overall chronic graft-versus-host disease was 53%. Treatment-related mortality was 17% at day +100 and 31% at 5 years. The 5-year relapse, event-free survival and overall survival rates were 31%, 36% and 44%, respectively. Although the event-free and overall survival rates in patients without BCR/ABL transcripts detectable at time of transplant were better than those in whom BCR/ABL transcripts were detected (46% versus 24% and 60% versus 30%, respectively) these differences were not statistically significant in the univariate analysis (P=0.07). These results demonstrate that umbilical cord blood transplantation from unrelated donors can be a curative treatment for a substantial number of patients with Philadelphia chromosome-positive acute lymphoblastic leukemia.

摘要

针对费城染色体阳性急性淋巴细胞白血病患者,采用脐带血移植进行治疗的效果,目前仅有少量专门针对该疾病的研究。我们报告了 45 例费城染色体阳性急性淋巴细胞白血病患者的治疗结果,这些患者均在 GETH/GITMO 合作组中接受了无关供体的清髓性单份脐带血移植。预处理方案基于噻替哌、白消安、环磷酰胺或氟达拉滨联合抗胸腺细胞球蛋白。在移植时,35 例患者(78%)处于完全缓解 1 期,4 例(8%)处于完全缓解 2 期,6 例(14%)处于第 3 期或后续缓解期。中位时间为 20 天时,骨髓嵌合率为 96%,且接受较高剂量 CD34+细胞的患者嵌合率更好。急性 2-4 级移植物抗宿主病的发生率为 31%,而总慢性移植物抗宿主病的发生率为 53%。移植后第 100 天和第 5 年的治疗相关死亡率分别为 17%和 31%。5 年复发率、无事件生存率和总生存率分别为 31%、36%和 44%。尽管在移植时未检测到 BCR/ABL 转录本的患者无事件生存率和总生存率优于检测到 BCR/ABL 转录本的患者(分别为 46%对 24%和 60%对 30%),但在单变量分析中这些差异无统计学意义(P=0.07)。这些结果表明,来自无关供体的脐带血移植可为大量费城染色体阳性急性淋巴细胞白血病患者提供治愈性治疗。

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Administration of imatinib after allogeneic hematopoietic stem cell transplantation may improve disease-free survival for patients with Philadelphia chromosome-positive acute lymphobla stic leukemia.异基因造血干细胞移植后给予伊马替尼治疗可能改善费城染色体阳性急性淋巴细胞白血病患者的无病生存。
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Single-unit umbilical cord blood transplantation from unrelated donors in patients with hematological malignancy using busulfan, thiotepa, fludarabine and ATG as myeloablative conditioning regimen.采用白消安、噻替哌、氟达拉滨和 ATG 作为清髓性预处理方案,对血液系统恶性肿瘤患者进行非血缘单份脐带血移植。
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