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双重膜滤过式血浆置换联合脱敏治疗单倍体相合造血干细胞移植供者特异性抗体的临床研究
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作者 王增胜 聂玉玲 +4 位作者 郎涛 张晓燕 蔺思颖 王晓敏 毛敏 《中国血液净化》 CSCD 2024年第1期22-25,共4页
目的探讨分析双重膜滤过式血浆置换(double filtration plasmapheresis,DFPP)联合脱敏治疗单倍体相合造血干细胞移植供者特异性抗体(donor specific antibody,DSA)的疗效。方法采用DFPP联合丙种免疫球蛋白(intravenous immunoglobulin,I... 目的探讨分析双重膜滤过式血浆置换(double filtration plasmapheresis,DFPP)联合脱敏治疗单倍体相合造血干细胞移植供者特异性抗体(donor specific antibody,DSA)的疗效。方法采用DFPP联合丙种免疫球蛋白(intravenous immunoglobulin,IVIG)、利妥昔单抗脱敏治疗DSA阳性患者,检测移植前后DSA水平,主要评估分析其植入情况。结果8例DSA性患者7例获得供者细胞稳定植入,嵌合率均为100%,1例血小板植入不良。经过DFPP、IVIG、利妥昔单抗脱敏处理后为平均荧光强度(mean fluorescence intensity,MFI)(3911±2499),均明显降低,差异均有统计学意义(t=2.101,P<0.001),8例患者中有3例转为弱阳性。干细胞回输第3天复测MFI(907士997),较干细胞回输前再次减低,差异均有统计学意义(t=2.145,P=0.002)。8例患者仅1例发生重度急性移植物抗宿主病。结论双重膜滤过式血浆置换脱敏联合大剂量IVIG和利妥昔单抗,尽量输注高剂量的干细胞,可以降低DSA水平促进供者干细胞植入。 展开更多
关键词 双重膜滤过式血浆置换 供者特异性抗体 单倍体相合造血干细胞移植
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Advances in haplo-identical stem cell transplantation in adults with high-risk hematological malignancies
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作者 Michael J Ricci Jeffrey A Medin Ronan S Foley 《World Journal of Stem Cells》 SCIE CAS 2014年第4期380-390,共11页
Allogeneic bone marrow transplant is a life-saving procedure for adults and children that have high-risk or relapsed hematological malignancies. Incremental advances in the procedure, as well as expanded sources of do... Allogeneic bone marrow transplant is a life-saving procedure for adults and children that have high-risk or relapsed hematological malignancies. Incremental advances in the procedure, as well as expanded sources of donor hematopoietic cell grafts have significantly improved overall rates of success. Yet, the outcomes for patients for whom suitable donors cannot be found remain a significant limitation. These patients may benefit from a hematopoietic cell transplant wherein a relative donor is fully haplotype mismatched. Previously this procedure was limited by graft rejection, lethal graft-versus-host disease, and increased treatmentrelated toxicity. Recent approaches in haplo-identical transplantation have demonstrated significantly improved outcomes. Based on years of incremental preclinical research into this unique form of bone marrow transplant, a range of approaches have now been studied in patients in relatively large phase Ⅱ trials that will be summarized in this review. 展开更多
关键词 Peripheral blood progenitors Stem cell transplantation GRAFT-VERSUS-HOST disease Haplo-identical DONOR HEMATOLOGICAL MALIGNANCIES
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一线单倍体造血干细胞移植或强化免疫抑制治疗中性粒细胞为0暴发型再生障碍性贫血研究 被引量:1
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作者 武利强 黄丽芳 +10 位作者 杨慧 叶宝东 沈建平 俞庆宏 庄海峰 杨岩 贾晋松 张东华 林圣云 何广胜 李建勇 《中国实用内科杂志》 CAS CSCD 北大核心 2021年第10期873-876,共4页
目的比较一线使用单倍体造血干细胞移植(HID-HSCT)或强化免疫抑制治疗(IST)治疗中性粒细胞为0的暴发型再生障碍性贫血(FAA)的疗效差异。方法收集2016年1月至2021年1月于中国贫血东部协作组各医院60例一线接受HID-HSCT或IST的中性粒细胞... 目的比较一线使用单倍体造血干细胞移植(HID-HSCT)或强化免疫抑制治疗(IST)治疗中性粒细胞为0的暴发型再生障碍性贫血(FAA)的疗效差异。方法收集2016年1月至2021年1月于中国贫血东部协作组各医院60例一线接受HID-HSCT或IST的中性粒细胞绝对值(ANC)为0的FAA的临床资料,回顾性分析比较2种治疗方法的疗效及预后。结果分别有25例、35例FAA患者接受HID-HSCT或IST治疗。HID-HSCT组和IST组相较:中位起效时间、6个月总反应率(ORR)、完全缓解(CR)均占显著优势:12.0(11.0,15.0)d比87.0(65.0,95.0)d,P<0.001;84.0%比40.0%,P=0.001;80.0%比17.1%,P=0.001。中位随访18.5(4.3,30.8)个月,HID-HSCT组无事件生存率(EFS)和总生存率(OS)均优于IST组(78.3%比20.0%,P=0.000;80.0%比57.1%,P=0.049)。结论HID-HSCT治疗FAA造血重建快,长期生存好,值得探索做为FAA一线治疗方案。 展开更多
关键词 再生障碍性贫血 暴发 中性粒细胞 单倍体造血干细胞移植 抗人胸腺细胞免疫球蛋白
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亲缘半相合与无关供者造血干细胞移植治疗重型再生障碍性贫血的疗效比较 被引量:8
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作者 卢岳 吴彤 +8 位作者 曹星玉 赵艳丽 刘德琰 孙瑞娟 熊敏 魏志杰 张建平 周葭蕤 陆道培 《中华血液学杂志》 CAS CSCD 北大核心 2016年第1期35-38,共4页
目的评价亲缘半相合造血干细胞移植(Haplo-HSCT)治疗重型再生障碍性贫血(SAA)的疗效,并且与同期进行的无关供者造血干细胞移植(UD-HSCT)进行比较。方法回顾性分析2012年9月至2014年7月接受替代供者造血干细胞移植的50例SAA患者... 目的评价亲缘半相合造血干细胞移植(Haplo-HSCT)治疗重型再生障碍性贫血(SAA)的疗效,并且与同期进行的无关供者造血干细胞移植(UD-HSCT)进行比较。方法回顾性分析2012年9月至2014年7月接受替代供者造血干细胞移植的50例SAA患者临床资料;其中24例接受HaploHSCT,26例接受UD-HSCT。结果中位随访时间9(2-26)个月,总生存(0s)率为91.3%。UD-HSCT组和Haplo—HSCT组0s率分别为96.1%和86.0%(P=0.30)。3例(6%)患者原发植入失败。Haplo—HSCT组患者Ⅱ-Ⅳ度急性移植物抗宿主病、慢性移植物抗宿主病、CMV血症、EBV血症发生率分别为37.5%、37.5%、78.2%及43.1%,均明显高于UD.HSCT组(3.83%、15.3%、46.1%及16.0%)(P值分别为0.003、0.030、0.005、0.040);出血性膀胱炎发生率差异无统计学意义(39.1%对23.0%,P=-0.120)。结论Haplo—HSCT治疗sAA0s率较高,疗效与UD—HSCT相近。 展开更多
关键词 造血干细胞移植 贫血 再生障碍性 重型 治疗结果 半相合供者 无关供者
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Comparison analysis between haplo identical stem cell transplantation and matched sibling donor stem cell transplantation for high-risk acute myeloid leukemia in first complete remission 被引量:9
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作者 Yang Liu Xiaojun Huang +6 位作者 Qian Fei Lanping Xu Xiaohui Zhang Kaiyan Liu Yuhong Chen Huan Chen Yu Wang 《Science China(Life Sciences)》 SCIE CAS CSCD 2019年第5期691-697,共7页
In order to compare the effect between haploidentical(HID) stem cell transplantation(HSCT) and matched sibling donor(MSD)stem cell transplantation for high-risk acute myeloid leukemia(AML) in first complete remission ... In order to compare the effect between haploidentical(HID) stem cell transplantation(HSCT) and matched sibling donor(MSD)stem cell transplantation for high-risk acute myeloid leukemia(AML) in first complete remission status(CR1), we retrospectively studied 170 cases who received stem cell transplantation from Jan 2008 to Jul 2015 in Peking University People's Hospital. We divided all cases into MSD group(43 cases) and HID(127 cases) group. Patients in HID and MSD group displayed similar baseline characteristics except for age distribution. There were no statistic differences for overall survival(OS), cumulative incidence of relapse, leukemia free survival(LFS), transplantation related mortality(TRM) between HID and MSD group. The 3-year OS, LFS for all patients was 63.9% and 59.7% respectively. Multivariate analysis showed that grade III-IV acute graft versus host disease(aGVHD) was an independent risk factor for treatment related mortality(HR=8.134, 95% CI:3.210–20.611, P<0.001), monosomy/complex chromosomal karyotype and white blood cell count more than 50×109 L-1 were two independent factors for relapse(HR=1.533, 95% CI: 1.040–2.260, P=0.031)(HR=1.004, 95% CI: 1.001–1.008, P=0.015).Grade III-IV aGVHD was an independent factor for mortality(HR=3.184, 95% CI: 1.718–5.902, P<0.001). These results demonstrated some risk factors for high-risk AML leukemia transplantation and indicated for AML patients in CR1 status, haplo stem cell transplantation could have the same therapeutic effect as MSD transplantation. 展开更多
关键词 high risk AML haplo stem cell TRANSPLANTATION matched SIBLING DONOR TRANSPLANTATION complex/monosomy CHROMOSOMAL KARYOTYPE
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