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三十例严重再生障碍性贫血“未输血”患者的骨髓移植

Marrow transplantation in thirty "untransfused" patients with severe aplastic anemia.

作者信息

Storb R, Thomas E D, Buckner C D, Clift R A, Deeg H J, Fefer A, Goodell B W, Sale G E, Sanders J E, Singer J, Stewart P, Weiden P L

出版信息

Ann Intern Med. 1980 Jan;92(1):30-6. doi: 10.7326/0003-4819-92-1-30.

Abstract

Thirty patients with severe aplastic anemia had no transfusions of blood products until just before marrow transplantation from HLA-identical family members. They were conditioned for grafting with cyclophosphamide, 50 mg/kg body weight on each of 4 successive days. All 30 had prompt initial marrow engraftment, which was sustained in 27. Twenty-five of the 30 are alive between 9 to 84 (median, 19.5) months. The actuarial projection of survival for 2 to 6 years is 75%. Twenty of the 25 surviving patients have no problems. Five have chronic graft-versus-host disease, resolving in two and active in three. Five patients died with infection or hemorrhage, four of whom had graft-versus-host disease. These data show that early transplantation should be carried out before transfusions are given for any patient with severe aplastic anemia who has an HLA-identical family member. If sensitization to minor transplantation antigens contained in blood products is avoided, the incidence of marrow-graft rejection will decrease, and survival will improve.

摘要

30例重型再生障碍性贫血患者在接受来自 HLA 配型相合的家庭成员的骨髓移植前均未输注血液制品。他们接受了环磷酰胺预处理以进行移植,连续4天,每天每千克体重给予50毫克环磷酰胺。所有30例患者均迅速实现了初始骨髓植入,其中27例得以维持。30例中有25例在9至84个月(中位数为19.5个月)之间存活。2至6年的生存精算预测为75%。25例存活患者中有20例没有问题。5例患有慢性移植物抗宿主病,其中2例病情缓解,3例病情仍在活动。5例患者死于感染或出血,其中4例患有移植物抗宿主病。这些数据表明,对于任何有 HLA 配型相合家庭成员的重型再生障碍性贫血患者,应在输血前尽早进行移植。如果避免对血液制品中所含次要移植抗原产生致敏,骨髓移植排斥反应的发生率将会降低,生存率将会提高。

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