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首页> 外文期刊>BMJ Open >Stem cell transplantation of matched sibling donors compared with immunosuppressive therapy for acquired severe aplastic anaemia: a Cochrane systematic review
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Stem cell transplantation of matched sibling donors compared with immunosuppressive therapy for acquired severe aplastic anaemia: a Cochrane systematic review

机译:相匹配的兄弟姐妹供体的干细胞移植与免疫抑制疗法治疗后天严重再生障碍性贫血的比较:一项Cochrane系统评价

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Objectives Acquired severe aplastic anaemia is a rare and potentially fatal disease. The aim of this Cochrane review was to evaluate the effectiveness and adverse events of first-line allogeneic haematopoietic stem cell transplantation of human leucocyte antigen (HLA)-matched sibling donors compared with first-line immunosuppressive therapy. Setting Specialised stem cell transplantations units in primary care hospitals. Participants We included 302 participants with newly diagnosed acquired severe aplastic anaemia. The age ranged from early childhood to young adulthood. We excluded studies on participants with secondary aplastic anaemia. Interventions We included allogeneic haematopoietic stem cell transplantation as the test intervention harvested from any source of matched sibling donor and serving as a first-line therapy. We included immunosuppressive therapy as comparator with either antithymocyte/antilymphocyte globulin or ciclosporin or a combination of the two. Primary and secondary outcome measures planned and finally measured The primary outcome was overall mortality. Secondary outcomes were treatment-related mortality, graft failure, graft-versus-host disease, no response to immunosuppressive therapy, relapse after initial successful treatment, secondary clonal disease or malignancies, health-related quality of life and performance scores. Results We identified three prospective non-randomised controlled trials with a study design that was consistent with the principle of ‘Mendelian randomisation’ in allocating patients to treatment groups. All studies had a high risk of bias due to the study design and were conducted more than 15?years. The pooled HR for overall mortality for the donor group versus the no donor group was 0.95 (95% CI 0.43 to 2.12, p=0.90). Conclusions There are insufficient and biased data that do not allow any firm conclusions to be made about the comparative effectiveness of first-line allogeneic haematopoietic stem cell transplantation of HLA-matched sibling donors and first-line immunosuppressive therapy of patients with acquired severe aplastic anaemia.
机译:目的获得性严重再生障碍性贫血是一种罕见且可能致命的疾病。这项Cochrane综述的目的是评估与一线免疫抑制疗法相比,与人白细胞抗原(HLA)匹配的同胞供体一线同种异体造血干细胞移植的有效性和不良事件。在基层医院设置专门的干细胞移植单位。参与者我们纳入了302名新诊断为获得性严重再生障碍性贫血的参与者。年龄从幼儿到成年。我们排除了继发再生障碍性贫血参与者的研究。干预措施我们包括同种异体造血干细胞移植,作为从任何匹配的同胞供体来源获得的测试干预措施,并作为一线治疗。我们将免疫抑制疗法作为抗胸腺细胞/抗淋巴细胞球蛋白或环孢菌素或两者的组合的对照。计划和最终测量的主要和次要结局指标主要结局是总体死亡率。次要结果是与治疗有关的死亡率,移植失败,移植物抗宿主病,对免疫抑制疗法无反应,初次成功治疗后复发,继发性克隆疾病或恶性肿瘤,与健康有关的生活质量和表现评分。结果我们确定了三项前瞻性非随机对照试验,其研究设计与将患者分配至治疗组的“孟德尔随机化”原理相一致。由于研究设计的原因,所有研究都有很高的偏倚风险,并且进行了15年以上。供体组与无供体组的总死亡率的合并HR为0.95(95%CI为0.43至2.12,p = 0.90)。结论目前尚无充分且有偏见的数据,无法就HLA匹配的同胞供体一线同种异体造血干细胞移植和获得性重度再生障碍性贫血患者的一线免疫抑制治疗的相对有效性做出确切的结论。

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