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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Donor, recipient, and transplant characteristics as risk factors after unrelated donor PBSC transplantation: beneficial effects of higher CD34+ cell dose.
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Donor, recipient, and transplant characteristics as risk factors after unrelated donor PBSC transplantation: beneficial effects of higher CD34+ cell dose.

机译:供体,受体和移植特性是无关供体PBSC移植后的危险因素:较高CD34 +细胞剂量的有益作用。

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We report outcomes of 932 recipients of unrelated donor peripheral blood stem cell hematopoietic cell transplantation (URD-PBSC HCT) for acute myeloid leukemia, acute lymphoblastic leukemia, chronic myelogenous leukemia, and myelodysplastic syndrome enrolled on a prospective National Marrow Donor Program trial from 1999 through 2003. Preparative regimens included myeloablative (MA; N = 611), reduced-intensity (RI; N = 160), and nonmyeloablative (NMA; N = 161). For MA recipients, CD34(+) counts greater than 3.8 x 10(6)/kg improved neutrophil and platelet engraftment, whereas improved overall survival (OS) and reduced transplant-related mortality (TRM) were seen for all preparative regimens when CD34(+) cell doses exceeded 4.5 x 10(6)/kg. Higher infused doses of CD34(+) cell dose did not result in increased rates of either acute or chronic graft-versus-host disease (GVHD). Three-year OS and disease-free survival (DFS) of recipients of MA, RI, and NMA approaches were similar (33%, 35%, and 32% OS; 33%, 30%, and 29% DFS, respectively). In summary, recipients of URD-PBSC HCT receiving preparative regimens differing in intensity experienced similar survival. Higher CD34(+) cell doses resulted in more rapid engraftment, less TRM, and better 3-year OS (39% versus 25%, MA, P = .004; 38% versus 21% RI/NMA, P = .004) but did not increase the risk of GVHD. This trial was registered at www.clinicaltrials.gov as #NCT00785525.
机译:我们报道了从1999年至2004年参加的一项前瞻性国家骨髓捐赠者计划试验所涉及的932名无相关供者外周血干细胞造血细胞移植(URD-PBSC HCT)的急性髓细胞性白血病,急性淋巴细胞性白血病,慢性粒细胞性白血病和骨髓增生异常综合征的患者2003。制备方案包括清髓性(MA; N = 611),强度降低(RI; N = 160)和非清髓性(NMA; N = 161)。对于MA接受者,CD34(+)计数大于3.8 x 10(6)/ kg时,嗜中性粒细胞和血小板移植改善了,而所有制备方案在CD34( +)细胞剂量超过4.5 x 10(6)/ kg。较高剂量的CD34(+)细胞注入剂量不会导致急性或慢性移植物抗宿主病(GVHD)的发生率增加。 MA,RI和NMA方法接受者的三年OS和无病生存期(DFS)相似(OS分别为33%,35%和32%; DFS分别为33%,30%和29%)。总之,接受强度不同的制备方案的URD-PBSC HCT受体的生存率相似。较高的CD34(+)细胞剂量可导致更快的植入,更少的TRM和更好的3年OS(39%vs 25%,MA,P = .004; 38%vs 21%RI / NMA,P = .004)但并未增加发生GVHD的风险。该试验已在www.clinicaltrials.gov上注册为#NCT00785525。

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