SDyshlevaia Z M, Skorobogatova E V, Maschan M A, Shipitsyna I P, Skvortsova Iu V, Trakhtman P E, Balashov D N, Pashko Iu V, Kurnikova E E, Suntsova E V, Goronkova O V, Solopova G G, Baĭdil'dina D D, Kalinina I I, Khachatrian L A, Shneĭder M M, Maschan A A
Ter Arkh. 2010;82(7):34-40.
To analyze the results of allogeneic and autologous hemopoietic cell transplantations (allo- and auto-HCT) in children with acute myeloid leukemia (AML) from an intermediate risk group, most of which were performed using lower-intensity conditioning modes. SUBJECTS AND METHODS. The study enrolled 36 children from an intermediate risk group, who had undergone auto-HCT (n = 22) or allo-HCT (n = 14) in December 1994 to December 2008. The patients' age was 0.7 to 16.6 years (median 12.8 years). Chemotherapeutic conditioning regimens were applied to all the patients. Melphalan was a basic myeloablative agent in 83.3% of cases.
With a median follow-up of 4.6 years (1.1-13.8 years), three-year relapse-free survival (RFS) was 80.4%; overall survival (OS) was 65.6%. Recurrences were documented only in 6 (16.6%) patients from the auto-HCT. Transplantation-associated mortality (TAM) was 13.8% (five patients died). After allo-HCT versus auto-HCT, RFS, OS, and TAM were 100 and 68.7% (p = 0.03), 93.2 and 55.5% (p = 0.02), and 7.1 and 18.2%, respectively. Acute and chronic graft-versus-host reactions developed in 57.1 and 23.1%, respectively.
Transplantation of allogeneic hemopoietic cells from a compatible related donor in the intermediate risk group children with AML, by using melphalan-based conditioning regimen, demonstrates a high survival rate with the minimum toxicity.
分析中危组急性髓系白血病(AML)患儿接受异基因和自体造血细胞移植(allo-HCT和auto-HCT)的结果,其中大多数移植采用了低强度预处理模式。对象与方法。本研究纳入了36例中危组患儿,他们在1994年12月至2008年12月期间接受了auto-HCT(n = 22)或allo-HCT(n = 14)。患者年龄为0.7至16.6岁(中位年龄12.8岁)。所有患者均采用了化疗预处理方案。83.3%的病例中马法兰是基本的清髓药物。
中位随访4.6年(1.1 - 13.8年),三年无复发生存率(RFS)为80.4%;总生存率(OS)为65.6%。仅6例(16.6%)接受auto-HCT的患者出现复发。移植相关死亡率(TAM)为13.8%(5例患者死亡)。allo-HCT与auto-HCT相比,RFS、OS和TAM分别为100%和68.7%(p = 0.03)、93.2%和55.5%(p = 0.02)以及7.1%和18.2%。急性和慢性移植物抗宿主反应的发生率分别为57.1%和23.1%。
对于中危组AML患儿,采用以马法兰为基础的预处理方案,从匹配的相关供体进行异基因造血细胞移植,显示出高生存率且毒性最小。