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骨髓增生异常综合征中 11 号三体定义了一组具有侵袭性临床病理特征的独特疾病。

Trisomy 11 in myelodysplastic syndromes defines a unique group of disease with aggressive clinicopathologic features.

机构信息

Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030-4009, USA.

出版信息

Leukemia. 2010 Apr;24(4):740-7. doi: 10.1038/leu.2009.289. Epub 2010 Jan 14.

Abstract

Trisomy 11 in myelodysplastic syndromes (MDS) is rare, with undefined clinical significance and is currently assigned to the International Prognostic Scoring System (IPSS) intermediate-risk group. Over a 15-year period, we identified 17 MDS patients with trisomy 11 either as a sole abnormality (n=10) or associated with one or two additional alterations (n=7), comprising 0.3% of all MDS cases reviewed. Of 16 patients with Bone Marrow material available for review, 14 (88%) patients presented with excess blasts, 69% patients evolved to acute myeloid leukemia (AML) in a 5-month median interval and the median survival was 14 months. For comparison, we studied 19 AML patients with trisomy 11 in a noncomplex karyotype, of which, a substantial subset of patients had morphologic dysplasia, and/or preexisting cytopenia(s)/MDS. Genomic DNA PCR showed MLL partial tandem duplication in 5 of 10 MDS and 7 of 11 AML patients. A review of literature identified 17 additional cases of MDS with trisomy 11, showing similar clinicopathologic features to our patients. Compared with our historical data comprising 1165 MDS patients, MDS patients with trisomy 11 had a significantly inferior survival to patients in the IPSS intermediate-risk cytogenetic group (P=0.0002), but comparable to the poor-risk group (P=0.97). We conclude that trisomy 11 in MDS correlates with clinical aggressiveness, may suggest an early/evolving AML with myelodysplasia-related changes and is best considered a high-risk cytogenetic abnormality in MDS prognostication.

摘要

三体 11 型在骨髓增生异常综合征(MDS)中较为罕见,其临床意义尚未明确,目前被归入国际预后评分系统(IPSS)的中危组。在过去的 15 年中,我们共发现了 17 例 MDS 患者存在三体 11,其或为单纯异常(n=10),或与一个或两个额外异常同时存在(n=7),占回顾性分析的所有 MDS 病例的 0.3%。在可用于回顾性分析的 16 例 MDS 患者中,14 例(88%)患者存在过量原始细胞,69%的患者在 5 个月的中位间隔内进展为急性髓系白血病(AML),中位生存期为 14 个月。相比之下,我们研究了 19 例非复杂核型的 AML 患者伴三体 11,其中许多患者存在形态学发育异常,和/或存在先前的血细胞减少症/ MDS。基因组 DNA PCR 显示,在 10 例 MDS 患者和 11 例 AML 患者中的 5 例和 7 例中存在 MLL 部分串联重复。文献回顾共发现了 17 例额外的 MDS 伴三体 11 病例,这些病例与我们的患者具有相似的临床病理特征。与我们包含 1165 例 MDS 患者的历史数据相比,MDS 伴三体 11 患者的生存明显劣于 IPSS 中危核型组的患者(P=0.0002),但与高危组相当(P=0.97)。我们得出结论,MDS 中的三体 11 与临床侵袭性相关,可能提示具有 MDS 相关改变的早期/进展性 AML,在 MDS 预后评估中最好被视为高危细胞遗传学异常。

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