mismatched unrelated donors

  • 文章类型: Journal Article
    NMDP认识到,尽管造血干细胞移植(HSCT)和其他细胞疗法取得了进展,并不是所有的病人都能得到公平的治疗,结果差距依然存在。本文探讨了NMDP的最新工作,通过变革性临床研究加速进展并扩大对更多患者的访问,特别是在使用不匹配的无关供体进行HSCT时。
    NMDP recognizes that despite advances in hematopoietic stem cell transplantation (HSCT) and other cell therapies, not all patients have equitable access to treatment, and disparities in outcomes remain. This paper explores the recent work of NMDP to accelerate progress and expand access to more patients through transformative clinical research, particularly in the use of mismatched unrelated donors for HSCT.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    对于缺乏匹配供体的高风险急性淋巴细胞白血病(ALL)患者,不匹配的无关供体(MMUD)和单倍体(haplo)移植都是有效的选择。
    该研究比较了2010-2020年接受9/10MMUD与单倍体移植联合移植后环磷酰胺(PTCy)作为移植物抗宿主病(GVHD)预防的成年ALL完全缓解(CR)患者的结局。
    该研究包括781名患者(MMUD,103;haplo,678).中位年龄为40岁(19-73岁)和38岁(18-75岁),分别(p=.51)。向PTCy中添加的最常见的免疫抑制剂是霉酚酸酯(MMF)/环孢菌素A和MMF/他克莫司。体内T细胞耗竭(抗胸腺细胞球蛋白)被给予21%和8%的移植,分别(p<0.0001)。中性粒细胞(绝对中性粒细胞计数>0.5×109/L)恢复分别为97.1%和96.7%(p=1)和MMUD和haplo,分别。MMUD和haplo之间的非复发死亡率和复发发生率没有显着差异,风险比(HR)=1.45(95%置信区间[CI],0.81-2.62;p=.21)和HR=0.81(95%CI,0.52-1.28,p=.38),分别。用于无白血病生存的HR,总生存率,无GVHD,无复发生存率分别为,HR=1.05(95%CI,0.73-1.50,p=.8),HR=1.17(95%CI,0.77-1.76,p=0.46),与MMUD相比,haplo的HR=1.07(95%CI,0.78-1.46,p=.7)。急性(a)GVHD2-4级明显较高,HR=1.73(95%CI,1.08-2.76,p=0.023),而aGVHD3-4级和慢性GVHD在两个移植组之间没有显着差异。
    对于所有CR患者,采用基于PTCy的GVHD预防的MMUD和单倍移植的结果相似,除了haplo移植的aGVHD发病率较高。
    Both mismatched unrelated donor (MMUD) and haploidentical (haplo) transplantation are valid options in patients with high-risk acute lymphoblastic leukemia (ALL) lacking a matched donor.
    The study compared the outcomes of adult patients with ALL in complete remission (CR) who underwent 9/10 MMUD versus haplo transplantation with posttransplant cyclophosphamide (PTCy) as graft-vs-host disease (GVHD) prophylaxis in 2010-2020.
    The study included 781 patients (MMUD, 103; haplo, 678). The median age was 40 (19-73) and 38 (18-75) years, respectively (p = .51). The most frequent immunosuppression agents added to PTCy were mycophenolate mofetil (MMF)/cyclosporine A and MMF/tacrolimus. In vivo T-cell depletion (anti-thymocyte globulin) was administered to 21% and 8% of the transplants, respectively (p < .0001). Neutrophil (absolute neutrophil count >0.5 × 109 /L) recovery was achieved in 97.1% versus 96.7% versus (p = 1) in MMUD and haplo, respectively. Nonrelapse mortality and relapse incidence were not significantly different between MMUD and haplo, hazard ratio (HR) = 1.45 (95% confidence interval [CI], 0.81-2.62; p = .21) and HR = 0.81 (95% CI, 0.52-1.28, p = .38), respectively. HRs for leukemia-free survival, overall survival, and GVHD-free, relapse-free survival were respectively, HR = 1.05 (95% CI, 0.73-1.50, p = .8), HR = 1.17 (95% CI, 0.77-1.76, p = .46), and HR = 1.07 (95% CI, 0.78-1.46, p = .7) for haplo compared to MMUD. Acute (a)GVHD grade 2-4 was significantly higher with haplo, HR = 1.73 (95% CI, 1.08-2.76, p = .023), whereas aGVHD grade 3-4 and chronic GVHD did not differ significantly between the two transplant groups.
    Outcomes of MMUD and haplo transplants with PTCy-based GVHD prophylaxis for ALL patients in CR are similar, apart from a higher incidence of aGVHD with haplo transplants.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

公众号