Michel G, Gluckman E, Blaise D, Esperou-Bourdeau H, Vernant J P, Kuentz M, Bordigoni P, Milpied N, Rubie H, Thuret I
Institut Paoli-Calmettes, Marseille, France.
J Clin Oncol. 1992 Dec;10(12):1865-9. doi: 10.1200/JCO.1992.10.12.1865.
We retrospectively analyzed the outcome of children with acute myeloid leukemia (AML) in first complete remission (CR) who received HLA-identical bone marrow transplantation (BMT) in 13 French transplant centers.
Seventy-four children were treated from June 1979 through December 1990. The conditioning regimen included total-body irradiation (TBI) in 54 cases and busulfan in 20. Prophylaxis of graft-versus-host disease (GVHD) consisted of cyclosporine (CycloA) plus methotrexate (MTX) for 38 patients, MTX for 17, CycloA for 18, and T depletion without other prophylaxis for one. The mean value of the interval from diagnosis to transplantation was 167 days.
Sixteen patients died of transplant-related complications, 12 relapsed, and 46 are alive in continuous remission with a median follow-up of 46 months. We examined results obtained over three successive periods: 1979 to 1982 (n = 14 children), 1983 to 1986 (n = 29), and 1987 to 1990 (n = 31). Probabilities of event-free survival (EFS) were 43%, 48%, and 82% for the three successive periods, respectively (P < .02). This improvement in EFS was linked to a decreased risk of transplant-related mortality: 36%, 36%, and 3%, respectively (P < .01). Other factors associated with a better EFS in the univariate analysis were a short time interval from diagnosis to transplant (< 120 days), the absence of significant (grade > or = 2) acute GVHD, and the absence of chronic GVHD. In the multivariate analysis, two factors had a favorable impact on long-term survival: the year of transplantation (years 1987 to 1990 v others) and the absence of acute GVHD.
The outcome for children receiving allogeneic BMT in first CR of AML has improved in France during recent years.
我们回顾性分析了13家法国移植中心中处于首次完全缓解(CR)期的急性髓系白血病(AML)患儿接受 HLA 相同的骨髓移植(BMT)后的结果。
1979年6月至1990年12月期间,74名患儿接受了治疗。预处理方案中,54例采用全身照射(TBI),20例采用白消安。38例患者采用环孢素(CycloA)加甲氨蝶呤(MTX)预防移植物抗宿主病(GVHD),17例采用 MTX,18例采用 CycloA,1例采用 T 细胞去除且无其他预防措施。从诊断到移植的间隔时间平均值为167天。
16例患者死于移植相关并发症,12例复发,46例仍存活且持续缓解,中位随访时间为46个月。我们分析了连续三个时期的结果:1979年至1982年(n = 14名患儿),1983年至1986年(n = 29),以及1987年至1990年(n = 31)。连续三个时期的无事件生存率(EFS)分别为43%、48%和82%(P < 0.02)。EFS 的这种改善与移植相关死亡率的降低有关:分别为36%、36%和3%(P < 0.01)。单因素分析中,与更好的 EFS 相关的其他因素包括从诊断到移植的时间间隔短(< 120天)、无显著(≥2级)急性 GVHD 以及无慢性 GVHD。多因素分析中,有两个因素对长期生存有有利影响:移植年份(1987年至1990年与其他年份相比)以及无急性 GVHD。
近年来,法国接受异基因 BMT 的 AML 首次 CR 期患儿的预后有所改善。