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急性髓系白血病首次缓解期接受异基因骨髓移植儿童的预后改善:骨髓移植研究组报告

Improvement in outcome for children receiving allogeneic bone marrow transplantation in first remission of acute myeloid leukemia: a report from the Groupe d'Etude des Greffes de Moelle Osseuse.

作者信息

Michel G, Gluckman E, Blaise D, Esperou-Bourdeau H, Vernant J P, Kuentz M, Bordigoni P, Milpied N, Rubie H, Thuret I

机构信息

Institut Paoli-Calmettes, Marseille, France.

出版信息

J Clin Oncol. 1992 Dec;10(12):1865-9. doi: 10.1200/JCO.1992.10.12.1865.

Abstract

PURPOSE

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.

PATIENTS AND METHODS

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.

RESULTS

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.

CONCLUSION

The outcome for children receiving allogeneic BMT in first CR of AML has improved in France during recent years.

摘要

目的

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。

患者与方法

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。

结果

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。

结论

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。

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