Phillips G L, Barnett M J, Brain M C, Chan K W, Huebsch L B, Klingemann H G, Meharchand J, Reece D E, Rybka W B, Shepherd J D
Leukemia/Bone Marrow Transplantation Program of British Columbia, Vancouver, General Hospital, Canada.
Bone Marrow Transplant. 1991 Dec;8(6):477-87.
Between February 1988 and January 1990, 35 patients underwent allogeneic bone marrow transplantation (BMT) from unrelated donors using measures routinely employed for matched related donors. Median patient age was 34 years (range 2-49). Thirty-two patients had hematologic malignancies, including chronic myelogenous leukemia (CML) in 16; three patients had severe aplastic anemia. Donor-patient pairs were matched at the HLA loci tested serologically (HLA-A, -B, -DR) in 29 cases; mixed leukocyte culture results were variable but often reactive. Five patients died prior to day +28 without evidence of myeloid engraftment, and one patient developed fatal graft failure several months after initial engraftment. Acute graft-versus-host disease (GVHD) occurred in 77% (95% confidence interval [CI] 60-90%) of all patients, and GVHD contributed to the death of 10 patients. Fatal regimen-related toxicity occurred in four patients and another died due to neurologic complications of a process that resembled the hemolytic-uremic syndrome. Two acute leukemia patients relapsed, and a CML patient was found to have a localized non-Hodgkin's lymphoma at necropsy. As of 1 June 1991, 14 patients are alive and in remission at a median follow-up of 1.9 years (range 1.5-3.3); all except one have normal performance scores. The 2-year actuarial event-free survival for all patients is 40% (95% CI 24-56%). Proportional hazards analysis revealed favorable significance for female patient sex, less advanced disease status and shorter interval from diagnosis to BMT. While unrelated-donor transplants need not necessarily duplicate the results of related-donor transplants to be of benefit, the event-free survival in this series was roughly similar to that expected in the related-donor situation, with the high transplant-related mortality somewhat offset by a low recurrence rate. Further studies using unrelated donors, employing new methods of preventing transplant-related complications, are indicated.
1988年2月至1990年1月期间,35例患者接受了来自无关供者的异基因骨髓移植(BMT),采用的是常用于匹配相关供者的措施。患者中位年龄为34岁(范围2 - 49岁)。32例患者患有血液系统恶性肿瘤,其中16例为慢性粒细胞白血病(CML);3例患者患有严重再生障碍性贫血。在29例中,供者与患者在血清学检测的HLA位点(HLA - A、- B、- DR)相匹配;混合淋巴细胞培养结果各异,但通常呈反应性。5例患者在+28天前死亡,无髓系植入证据,1例患者在初次植入数月后发生致命的移植失败。77%(95%置信区间[CI] 60 - 90%)的患者发生了急性移植物抗宿主病(GVHD),GVHD导致10例患者死亡。4例患者发生了致命的与预处理方案相关的毒性反应,另1例患者因类似溶血尿毒综合征的过程出现神经并发症而死亡。2例急性白血病患者复发,1例CML患者尸检时发现有局限性非霍奇金淋巴瘤。截至1991年6月1日,14例患者存活且处于缓解状态,中位随访时间为1.9年(范围1.5 - 3.3年);除1例患者外,所有患者的体能评分均正常。所有患者的2年无事件生存率为40%(95% CI 24 - 56%)。比例风险分析显示,女性患者性别、疾病状态较早期以及从诊断到BMT的间隔时间较短具有有利意义。虽然无关供者移植不一定需要重复相关供者移植的结果才能有益,但本系列中的无事件生存率与相关供者情况下预期的大致相似,较高的移植相关死亡率在一定程度上被较低的复发率所抵消。有必要采用预防移植相关并发症的新方法,对无关供者进行进一步研究。