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系统性肥大细胞增多症在 KIT D816V 突变阳性的伴有重现性遗传学异常的急性髓系白血病中不常见。

Systemic mastocytosis is uncommon in KIT D816V mutation positive core-binding factor acute myeloid leukemia.

机构信息

Department of Pathology, Odense University Hospital, Odense, Denmark.

出版信息

Leuk Lymphoma. 2012 Jul;53(7):1338-44. doi: 10.3109/10428194.2011.647314. Epub 2012 Jan 31.

Abstract

The KIT D816V mutation is detected in the vast majority of adult cases of systemic mastocytosis (SM). The mutation is also frequently detected in core-binding factor acute myeloid leukemia (CBF AML) defined by the presence of t(8;21)(q22;q22); RUNX1-RUNX1T1 or inv(16)(p13.1;q22)/t(16;16)(p13.1;q22); CBFB-MYH11 chromosomal rearrangements, but whether the mutation is indicative of associated SM is unclear. In the present study, patients with CBF AML were therefore analyzed for the KIT D816V mutation and mutation positive cases subsequently analyzed for the presence of SM. The KIT D816V mutation was detected in eight of 20 cases of CBF AML, with the frequency in t(8;21)(q22;q22) and inv(16)(p13.1;q22) positive cases being 31% and 57%, respectively. The fraction of KIT D816V mutation positive cells was highly variable among the eight mutation positive patients, with levels ranging from 0.04 to 98% in a pretreatment blood sample. Five of the eight cases carried the mutation in a cell fraction below one-tenth of the blast cell fraction, thus suggesting that KIT mutation is often a late event in leukemogenesis. None of the eight KIT D816V mutation positive cases fulfilled the World Health Organization diagnostic criteria of SM. The presence of the KIT D816V mutation in the CBF AML subgroup can therefore not be considered indicative of associated SM.

摘要

KIT D816V 突变在绝大多数系统性肥大细胞增多症(SM)的成年病例中被检测到。该突变也经常在核心结合因子急性髓系白血病(CBF AML)中被检测到,其定义为存在 t(8;21)(q22;q22); RUNX1-RUNX1T1 或 inv(16)(p13.1;q22)/t(16;16)(p13.1;q22); CBFB-MYH11 染色体重排,但该突变是否提示相关的 SM 尚不清楚。因此,在本研究中,对 CBF AML 患者进行了 KIT D816V 突变分析,并对突变阳性病例进行了 SM 存在的分析。在 20 例 CBF AML 中,检测到 8 例存在 KIT D816V 突变,在 t(8;21)(q22;q22)和 inv(16)(p13.1;q22)阳性病例中的频率分别为 31%和 57%。在 8 例突变阳性患者中,KIT D816V 突变阳性细胞的比例高度可变,在预处理血液样本中的水平范围为 0.04%至 98%。在 8 例病例中,有 5 例的突变细胞比例低于原始细胞的十分之一,这表明 KIT 突变通常是白血病发生的晚期事件。在这 8 例 KIT D816V 突变阳性病例中,均不符合 SM 的世界卫生组织诊断标准。因此,CBF AML 亚组中 KIT D816V 突变的存在不能被认为与相关的 SM 相关。

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