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原发性和继发性骨髓增生异常综合征的细胞遗传学发现。

Cytogenetic findings in primary and secondary MDS.

作者信息

Heim S

机构信息

Department of Clinical Genetics, University Hospital, Lund, Sweden.

出版信息

Leuk Res. 1992;16(1):43-6. doi: 10.1016/0145-2126(92)90098-r.

DOI:10.1016/0145-2126(92)90098-r
PMID:1732669
Abstract

More than 1300 MDS cases with clonal cytogenetic abnormalities, 200 of them secondary MDS, have been reported. The most common aberrations in primary MDS are del(5q) (27%), trisomy 8 (19%), monosomy 7 (15%), der(11q) (7%), -5, der(12p) and -Y (5%), del(7q) (4%), and t(1;7), der(3q), del(13q), i(17q) and del(20q) in 2% or less. The 5q- is mostly, but not always, a del(5)(q13q33); it is the cytogenetic hall-mark of the "5q- syndrome" and is frequently found as the sole abnormality. The frequency of the aberrations varies among MDS subgroups: 5q- is most frequent in RA, -5, -7, and der(12p) are more common in CMML and especially in RAEB, and +8 and der(11q) are more often found in RARS. The most common aberrations in secondary MDS are -7 (41%), del(5q) (28%), -5 (11%), der(21q) (9%), 7q-, +8 and der(12p) (8%), t(1;7) and -12 (7%), der(17p) (6%), der(3p) and der(6p) (5%), and der(3q), der(11q), -17, -18 and der(19q) (4%). The average number of abnormalities per case is 5.3, compared with 2.9 in unspecified MDS. The frequency of cytogenetically unrelated clones is 5.7% in secondary and 4.3% in primary MDS. When the literature data are broken down by type of genotoxic exposure, it turns out that -5, -7, and der(17p) are over-represented in patients who have received chemotherapy, whereas 5q- is associated with no exposure or preceding radiotherapy only. The karyotypic profile is prognostically important: patients with -7 or complex karyotypes have a higher risk of progression to acute leukemia and shorter survival.

摘要

已报告了1300多例伴有克隆性细胞遗传学异常的骨髓增生异常综合征(MDS)病例,其中200例为继发性MDS。原发性MDS中最常见的畸变是del(5q)(27%)、三体8(19%)、单体7(15%)、der(11q)(7%)、-5、der(12p)和-Y(5%)、del(7q)(4%),以及t(1;7)、der(3q)、del(13q)、i(17q)和del(20q)(2%或更低)。5q-大多但不总是del(5)(q13q33);它是“5q-综合征”的细胞遗传学标志,常作为唯一异常被发现。畸变的频率在MDS亚组中有所不同:5q-在难治性贫血(RA)中最常见,-5、-7和der(12p)在慢性粒-单核细胞白血病(CMML)尤其是难治性贫血伴原始细胞过多(RAEB)中更常见,而+8和der(11q)在难治性贫血伴环形铁粒幼细胞增多(RARS)中更常出现。继发性MDS中最常见的畸变是-7(41%)、del(5q)(28%)、-5(11%)、der(21q)(9%)、7q-、+8和der(12p)(8%)、t(1;7)和-12(7%)、der(17p)(6%)、der(3p)和der(6p)(5%),以及der(3q)、der(11q)、-17、-18和der(19q)(4%)。每例异常的平均数量为5.3,而未分类的MDS为2.9。细胞遗传学不相关克隆的频率在继发性MDS中为5.7%,在原发性MDS中为4.3%。当按遗传毒性暴露类型对文献数据进行分类时,结果显示-5、-7和der(17p)在接受化疗的患者中过度出现,而5q-仅与无暴露或先前的放疗相关。核型图谱在预后方面很重要:伴有-7或复杂核型的患者进展为急性白血病的风险更高,生存期更短。

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