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Characteristics and outcome of patients with acute myeloid leukemia refractory to 1 cycle of high-dose cytarabine-based induction chemotherapy.对 1 周期高剂量阿糖胞苷为基础的诱导化疗难治的急性髓细胞白血病患者的特征和结局。
Blood. 2010 Dec 23;116(26):5818-23; quiz 6153. doi: 10.1182/blood-2010-07-296392. Epub 2010 Oct 5.
2
Donor-recipient mismatches in MHC class I chain-related gene A in unrelated donor transplantation lead to increased incidence of acute graft-versus-host disease.在无关供体移植中,主要组织相容性复合体I类链相关基因A的供体-受体错配会导致急性移植物抗宿主病的发病率增加。
Blood. 2009 Oct 1;114(14):2884-7. doi: 10.1182/blood-2009-05-223172. Epub 2009 Aug 4.
3
Reduced intensity conditioning compared with myeloablative conditioning using unrelated donor transplants in patients with acute myeloid leukemia.与采用清髓性预处理的无关供者移植相比,急性髓系白血病患者采用减低强度预处理的无关供者移植。
J Clin Oncol. 2009 Sep 20;27(27):4570-7. doi: 10.1200/JCO.2008.20.9692. Epub 2009 Aug 3.
4
Reduced-toxicity conditioning therapy with allogeneic stem cell transplantation for acute leukemia.异基因干细胞移植治疗急性白血病的低毒性预处理疗法
Curr Opin Oncol. 2009 Jun;21 Suppl 1(Suppl 1):S11-5. doi: 10.1097/01.cco.0000357469.83960.12.
5
Allogeneic stem cell transplantation for acute myeloid leukemia in first complete remission: systematic review and meta-analysis of prospective clinical trials.首次完全缓解的急性髓系白血病患者的异基因干细胞移植:前瞻性临床试验的系统评价和荟萃分析
JAMA. 2009 Jun 10;301(22):2349-61. doi: 10.1001/jama.2009.813.
6
Busulfan in hematopoietic stem cell transplantation.白消安在造血干细胞移植中的应用
Biol Blood Marrow Transplant. 2009 May;15(5):523-36. doi: 10.1016/j.bbmt.2008.12.489. Epub 2009 Feb 12.
7
Low-dose azacitidine after allogeneic stem cell transplantation for acute leukemia.急性白血病异基因干细胞移植后使用低剂量阿扎胞苷
Cancer. 2009 May 1;115(9):1899-905. doi: 10.1002/cncr.24198.
8
Once daily i.v. busulfan and fludarabine (i.v. Bu-Flu) compares favorably with i.v. busulfan and cyclophosphamide (i.v. BuCy2) as pretransplant conditioning therapy in AML/MDS.作为急性髓系白血病/骨髓增生异常综合征(AML/MDS)移植前预处理疗法,每日一次静脉注射白消安和氟达拉滨(静脉注射Bu-Flu)与静脉注射白消安和环磷酰胺(静脉注射BuCy2)相比具有优势。
Biol Blood Marrow Transplant. 2008 Jun;14(6):672-84. doi: 10.1016/j.bbmt.2008.03.009.
9
High busulfan exposure is associated with worse outcomes in a daily i.v. busulfan and fludarabine allogeneic transplant regimen.在每日静脉注射白消安和氟达拉滨的异基因移植方案中,高剂量白消安暴露与更差的预后相关。
Biol Blood Marrow Transplant. 2008 Feb;14(2):220-8. doi: 10.1016/j.bbmt.2007.10.028.
10
The role of cytotoxic therapy with hematopoietic stem cell transplantation in the therapy of acute myelogenous leukemia in adults: an evidence-based review.细胞毒性疗法联合造血干细胞移植在成人急性髓性白血病治疗中的作用:一项循证综述
Biol Blood Marrow Transplant. 2008 Feb;14(2):137-80. doi: 10.1016/j.bbmt.2007.11.002.

无关供者移植治疗急性髓细胞白血病缓解后。

Unrelated donor transplantation for acute myelogenous leukemia in first remission.

机构信息

Department of Stem Cell Transplantation and Cellular Therapy, U.T. M.D. Anderson Cancer Center, Houston, Texas 77030-4009, USA.

出版信息

Biol Blood Marrow Transplant. 2011 Jul;17(7):1067-71. doi: 10.1016/j.bbmt.2010.11.012. Epub 2010 Nov 16.

DOI:10.1016/j.bbmt.2010.11.012
PMID:21087679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4080632/
Abstract

We retrospectively analyzed the outcomes of all acute myelogenous leukemia (AML) patients in first remission (n = 44; median age = 48 years; high-risk cytogenetics = 59%) who received unrelated donor hematopoietic cell transplantation (HCT) with myeloablative conditioning regimen of i.v. busulfan, fludarabine, and antithymocyte globulin (ATG) between January 2002 and November 2009 at our institution. Donor-recipient pairs were matched by high-resolution HLA-A, -B, -C, -DRB1, and -DQB1 typing (10/10 matches, n = 41; 9/10 matches, n = 3). With a median follow-up of 34 months, actuarial 3-year event-free survival (EFS) and overall survival (OS) is 70% and 78%, respectively. The 3-year EFS and OS in patients with and without poor risk cytogenetics is similar (63% versus 82%, P = 0.43 and 78% versus 82%, P = .89, respectively). The 3-year EFS and OS is also similar in patients above age 55 year versus patients age 55 year or younger (80% versus 67%, P = .47 and 80% versus 78%, P = .81, respectively). The 100-day and 3-year cumulative incidence of transplant-related mortality is 5% and 15%, respectively. Six patients have relapsed, and 3 of them are alive and in remission after salvage therapy, with a median follow-up of 23 months. These results indicate that the majority of AML patients eligible for this treatment can achieve long-term disease control.

摘要

我们回顾性分析了在我们机构接受了异基因造血细胞移植(HCT)且符合条件的所有 44 例处于首次缓解期(AML)患者的结果(中位年龄 48 岁;高危细胞遗传学 59%)。该治疗采用 IV 布美他尼、氟达拉滨和抗胸腺细胞球蛋白(ATG)的清髓性预处理方案,于 2002 年 1 月至 2009 年 11 月进行。供体-受者对通过高分辨率 HLA-A、-B、-C、-DRB1 和-DQB1 分型进行匹配(10/10 匹配,n=41;9/10 匹配,n=3)。中位随访 34 个月后,无事件生存(EFS)和总生存(OS)的 3 年累计发生率分别为 70%和 78%。细胞遗传学低危和高危患者的 3 年 EFS 和 OS 相似(63%对 82%,P=0.43 和 78%对 82%,P=0.89)。55 岁以上和 55 岁以下患者的 3 年 EFS 和 OS 也相似(80%对 67%,P=0.47 和 80%对 78%,P=0.81)。100 天和 3 年移植相关死亡率的累积发生率分别为 5%和 15%。6 例患者复发,其中 3 例在挽救治疗后仍存活且处于缓解期,中位随访时间为 23 个月。这些结果表明,大多数符合该治疗条件的 AML 患者可获得长期疾病控制。