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[AML-BFM-78和-83研究中嗜酸性粒细胞增多在儿童急性髓系白血病中的预后意义]

[Prognostic significance of eosinophilia in children with acute myeloid leukemia in the studies AML-BFM-78 and -83].

作者信息

Creutzig U, Ritter J, Niederbiermann-Koczy G, Harbott J, Schellong G

机构信息

Universitäts-Kinderklinik Münster.

出版信息

Klin Padiatr. 1989 Jul-Aug;201(4):220-6. doi: 10.1055/s-2007-1025307.

Abstract

Initial eosinophilia (greater than or equal to 3%) in the bone marrow was found in 73 out of 269 (27%) patients studied in AML studies BFM-78 and -83. It was predominantly seen in children with FAB types M2 (44%) and M4 (41%). Atypical eosinophils were mostly found in FAB type M4 (20/28 = 71%). Cytogenetic studies in eight children with FAB M4 and eosinophilia showed normal karyotypes in four patients, inversion 16 in one and other aberrations in three children. Study AML-BFM-78 did not demonstrate any differences in prognosis between patients with and without eosinophilia (event-free survival = EFS after 5 years 37%, SD 8%, vs. 38%, SD 6%). In study AML-BFM-83, however, a clear increase in EFS was seen in children with eosinophilia (EFS 72%, SD 8%, vs. 43%, SD 5%, p = 0.001). This improvement of prognosis mainly concerns patients with FAB M4 and eosinophilia (EFS 81%, SD 10%, vs. 23%, SD 11%, p = 0.006). None of the 12 children in study AML-BFM-83 with FAB M4 and atypical eosinophils has suffered a relapse, two patients belong to the early death group. Multivariate analysis shows only eosinophilia as a favorable prognostic factor in FAB type M4. According to these results FAB type M 4 with eosinophilia is a favorable prognostic parameter in children treated according to the therapy protocol of study AML-BFM-83.

摘要

在AML研究BFM - 78和 - 83中,对269例患者进行研究,发现73例(27%)患者骨髓中初始嗜酸性粒细胞增多(大于或等于3%)。这主要见于FAB分型为M2(44%)和M4(41%)的儿童。非典型嗜酸性粒细胞大多见于FAB分型为M4的患者(20/28 = 71%)。对8例FAB M4型且伴有嗜酸性粒细胞增多的儿童进行细胞遗传学研究,结果显示4例患者核型正常,1例为16号染色体倒位,3例儿童有其他畸变。AML - BFM - 78研究未显示有嗜酸性粒细胞增多和无嗜酸性粒细胞增多的患者在预后方面有任何差异(5年无事件生存率 = EFS,有嗜酸性粒细胞增多患者为37%[标准差8%],无嗜酸性粒细胞增多患者为38%[标准差6%])。然而,在AML - BFM - 83研究中,嗜酸性粒细胞增多的儿童EFS明显增加(EFS为72%[标准差8%],无嗜酸性粒细胞增多儿童为43%[标准差5%],p = 0.001)。这种预后改善主要涉及FAB M4型且伴有嗜酸性粒细胞增多的患者(EFS为81%[标准差10%],无嗜酸性粒细胞增多患者为23%[标准差11%],p = 0.006)。在AML - BFM - 83研究中,12例FAB M4型且伴有非典型嗜酸性粒细胞的儿童均未复发,2例患者属于早期死亡组。多因素分析显示,在FAB M4型中,只有嗜酸性粒细胞增多是一个有利的预后因素。根据这些结果,在按照AML - BFM - 83研究的治疗方案进行治疗的儿童中FAB M4型伴嗜酸性粒细胞增多是一个有利的预后参数。

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