Deeg H J, Storb R, Thomas E D, Appelbaum F, Buckner C D, Clift R A, Doney K, Johnson L, Sanders J E, Stewart P, Sullivan K M, Witherspoon R P
Blood. 1983 May;61(5):954-9.
Eight patients with Fanconi's anemia were given cyclophosphamide alone (seven patients) or combined with procarbazine and antithymocyte globulin (one patient) followed by marrow grafts from HLA-identical siblings. All patients had engraftment. Seven developed acute and three chronic graft-versus-host disease (GVHD). Three patients died with GVHD and infectious complications (days 19, 56, and 82) and one with an intracerebral hemorrhage (day 540). Four patients are surviving 647-3435 days after grafting, two are well, and two have chronic GVHD that is improving. These results show that Fanconi's anemia can be treated successfully by allogeneic marrow transplantation.
8例范可尼贫血患者单独接受环磷酰胺治疗(7例),或联合丙卡巴肼和抗胸腺细胞球蛋白治疗(1例),随后接受来自 HLA 相同同胞的骨髓移植。所有患者均实现植入。7例发生急性移植物抗宿主病(GVHD),3例发生慢性GVHD。3例患者死于GVHD和感染并发症(分别在第19、56和82天),1例死于脑出血(第540天)。4例患者在移植后647 - 3435天存活,2例情况良好,2例慢性GVHD正在改善。这些结果表明,异基因骨髓移植可成功治疗范可尼贫血。