Anasetti C, Doney K C, Storb R, Meyers J D, Farewell V T, Buckner C D, Appelbaum F R, Sullivan K M, Clift R A, Deeg H J
Ann Intern Med. 1986 Apr;104(4):461-6. doi: 10.7326/0003-4819-104-4-461.
Fifty patients with severe aplastic anemia had no transfusions of blood products until just before marrow transplantation from HLA-identical family members. Of the 50, 42 are still alive 1 to 12 years after transplantation (median, 7 years). By actuarial standards, the 10-year probability of survival is 82%. Of the 42 surviving patients, 37 have Karnofsky performance status scores of 100% and 5 with chronic graft-versus-host disease have scores ranging from 50% to 90% (median, 80%). The 8 deaths were caused by early infection in 1, graft rejection in 1, acute graft-versus-host disease in 3, and chronic graft-versus-host disease in 3. All deaths occurred within two years after transplantation. The incidence of graft failure was 10%. Acute graft-versus-host disease developed in 14 of 44 patients at risk and chronic graft-versus-host disease, in 15 of 41. Risk factors for development of chronic graft-versus-host disease included increased age (p = 0.008) and presence of acute graft-versus-host disease (p = 0.001). The only factor associated with increased risk of death was development of acute graft-versus-host disease (p = 0.05). Results of this study extend our previous finding that patients with severe aplastic anemia who have transplants before the onset of transfusion-induced sensitization have an excellent probability of long-term survival and a normal life.
50例严重再生障碍性贫血患者在接受来自 HLA 配型相同家庭成员的骨髓移植前均未输注血液制品。这50例患者中,42例在移植后1至12年仍存活(中位数为7年)。按照精算标准,10年生存率为82%。在42例存活患者中,37例卡氏评分100%,5例患有慢性移植物抗宿主病,评分在50%至90%之间(中位数为80%)。8例死亡原因分别为:1例早期感染,1例移植排斥,3例急性移植物抗宿主病,3例慢性移植物抗宿主病。所有死亡均发生在移植后两年内。移植失败发生率为10%。44例有风险的患者中有14例发生了急性移植物抗宿主病,41例中有15例发生了慢性移植物抗宿主病。慢性移植物抗宿主病发生的风险因素包括年龄增加(p = 0.008)和存在急性移植物抗宿主病(p = 0.001)。与死亡风险增加相关的唯一因素是发生急性移植物抗宿主病(p = 0.05)。本研究结果扩展了我们之前的发现,即严重再生障碍性贫血患者在输血诱导的致敏反应发生之前进行移植,有极好的长期生存概率和正常生活的可能性。