首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Cytogenetic aberrations and their prognostic value in a series of 330 splenic marginal zone B-cell lymphomas: a multicenter study of the Splenic B-Cell Lymphoma Group.
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Cytogenetic aberrations and their prognostic value in a series of 330 splenic marginal zone B-cell lymphomas: a multicenter study of the Splenic B-Cell Lymphoma Group.

机译:在一系列330例脾脏边缘区B细胞淋巴瘤中的细胞遗传学异常及其预后价值:脾脏B细胞淋巴瘤组的多中心研究。

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摘要

We conducted a retrospective collaborative study to cytogenetically characterize splenic marginal zone lymphoma (SMZL) and ascertain the prognostic value of chromosomal aberrations. Of 330 cases, 72% displayed an aberrant karyotype, 53% were complex, and 29% had a single aberration. The predominant aberrations were gains of 3/3q and 12q, deletions of 7q and 6q and translocations involving 8q/1q/14q. CD5 expression was detected in 39 of 158 cases (25%). The cytogenetic makeup of the CD5(+) group differed significantly from that of the CD5(-) group. Cases with unmutated IGHV were significantly associated with deletions of 7q and TP53. A strong association was noted between usage of the IGVH1-2 and deletion 7q, 14q alterations, and abnormal karyotype. On univariate analysis, patients with more than or equal to 2 aberrations, 14q alterations, and TP53 deletions had the shortest survival; 7q deletion did not affect survival. On multivariate analysis, cytogenetic aberrations did not retain prognostic significance; the parameters negatively affecting survival were hemoglobin and age. In conclusion, the cytogenetic profile of SMZL is distinct from other B-cell lymphomas. Complexity of the karyotype, 14q aberrations, and TP53 deletions are poor prognostic indicators and may be considered together with other clinicobiologic parameters to ascertain the prognosis of SMZL.
机译:我们进行了一项回顾性合作研究,以细胞学方式分析脾边缘区淋巴瘤(SMZL)并确定染色体畸变的预后价值。在330例病例中,有72%表现出异常的核型,53%表现出复杂的,29%表现出单一的畸变。主要像差为3 / 3q和12q,缺失7q和6q以及易位涉及8q / 1q / 14q。 158例病例中有39例检测到CD5表达(25%)。 CD5(+)组的细胞遗传组成与CD5(-)组的显着不同。 IGHV未突变的病例与7q和TP53的缺失显着相关。注意到IGVH1-2的使用与缺失7q,14q改变和异常核型之间存在密切关联。单因素分析显示,畸变大于或等于2、14q改变和TP53缺失的患者生存期最短。 7q删除不影响生存。在多变量分析中,细胞遗传学异常并没有保留预后意义。对生存不利的参数是血红蛋白和年龄。总之,SMZL的细胞遗传学特征不同于其他B细胞淋巴瘤。核型,14q畸变和TP53缺失的复杂性是不良的预后指标,可以与其他临床生物学参数一起考虑以确定SMZL的预后。

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