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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Haploidentical transplant with posttransplant cyclophosphamide vs matched unrelated donor transplant for acute myeloid leukemia
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Haploidentical transplant with posttransplant cyclophosphamide vs matched unrelated donor transplant for acute myeloid leukemia

机译:单倍体移植与环磷酰胺移植后与配对非相关供体移植治疗急性髓细胞白血病

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We studied adults with acute myeloid leukemia (AML) after haploidentical (n = 192) and 8/8 HLA-matched unrelated donor (n = 1982) transplantation. Haploidentical recipients received calcineurin inhibitor (CNI), mycophenolate, and posttransplant cyclophosphamide for graft-versus-host disease (GVHD) prophylaxis; 104 patients received myeloablative and 88 received reduced intensity conditioning regimens. Matched unrelated donor transplant recipients received CNI with mycophenolate or methotrexate for GVHD prophylaxis; 1245 patients received myeloablative and 737 received reduced intensity conditioning regimens. In the myeloablative setting, day 30 neutrophil recovery was lower after haploidentical compared with matched unrelated donor transplants (90% vs 97%, P = .02). Corresponding rates after reduced intensity conditioning transplants were 93% and 96% (P = .25). In the myeloablative setting, 3-month acute grade 2-4 (16% vs 33%, P < .0001) and 3-year chronic GVHD (30% vs 53%, P < .0001) were lower after haploidentical compared with matched unrelated donor transplants. Similar differences were observed after reduced intensity conditioning transplants, 19% vs 28% (P = .05) and 34% vs 52% (P = .002). Among patients receiving myeloablative regimens, 3-year probabilities of overall survival were 45% (95% CI, 36-54) and 50% (95% CI, 47-53) after haploidentical and matched unrelated donor transplants (P5.38). Corresponding rates after reduced intensity conditioning transplants were 46%(95% CI, 35-56) and 44% (95% CI, 0.40-47) (P = .71). Although statistical poweris limited, these data suggests that survival for patients with AML after haploidentical transplantation with posttransplant cyclophosphamide is comparable with matched unrelated donor transplantation.
机译:我们研究了单倍体移植(n = 192)和8/8 HLA匹配无关供体(n = 1982)移植后的成人急性髓细胞白血病(AML)。单倍体接受者接受钙调神经磷酸酶抑制剂(CNI),霉酚酸酯和移植后环磷酰胺预防移植物抗宿主病(GVHD); 104例患者接受了清髓治疗,88例接受了强度降低的治疗方案。配对的非相关供体移植受者接受了CNI和霉酚酸酯或甲氨蝶呤预防GVHD; 1245例患者接受了清髓治疗,而737例接受了降低强度的调理方案。在清髓性设置中,与匹配的无关供体移植相比,单倍后第30天的中性粒细胞恢复较低(90%比97%,P = .02)。降低强度的条件移植后的相应发生率分别为93%和96%(P = .25)。在清髓性设置中,单人后3个月急性2-4级(16%vs 33%,P <.0001)和3年慢性GVHD(30%vs 53%,P <.0001)低于配对不相关的供体移植。降低强度的条件移植后,观察到相似的差异,分别为19%vs. 28%(P = .05)和34%vs 52%(P = .002)。在接受清髓疗法的患者中,单倍体和相配的无关供体移植后3年总生存率分别为45%(95%CI,36-54)和50%(95%CI,47-53)(P5.38)。降低强度的条件移植后的相应发生率分别为46%(95%CI,35-56)和44%(95%CI,0.40-47)(P = .71)。尽管统计能力有限,但这些数据表明,移植后环磷酰胺单倍体移植后AML患者的存活率与匹配的无关供体移植相当。

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