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慢性淋巴细胞白血病的结构改变。细胞遗传学和 FISH 分析。

Structural alterations in chronic lymphocytic leukaemia. Cytogenetic and FISH analysis.

机构信息

Laboratorio de Genética, Instituto de Medicina Experimental (IMEX) CONICET- Academia Nacional de Medicina, Buenos Aires, Argentina.

出版信息

Hematol Oncol. 2013 Jun;31(2):79-87. doi: 10.1002/hon.2025. Epub 2012 Sep 7.

Abstract

In this study, we described cytogenetics and fluorescence in situ hybridization (FISH) analysis performed in chronic lymphocytic leukaemia (CLL) patients with structural alterations. Results were correlated with clinical characteristics. A total of 38 CLL patients: 16 cases with complex and 22 with simple karyotypes were studied. For comparison of clinical parameters, a control group of 78 CLL patients with normal karyotype and without FISH genomic alterations were also evaluated. We found 38 structural abnormalities not previously described in the literature, 28 (74%) of them were translocations. In cases with complex karyotypes, chromosomes 6, 8 and 13 were the most frequently involved in new alterations (nine each), followed by chromosomes 12, 14 and 15 (six each). Chromosome 8p was particularly involved in losses, being 8p21-pter the commonest region of overlap. Cases with simple karyotypes, showed del(6q) as the most frequent alteration (39%). Del(9)(q11) was recurrent in our series. Analysis of clinical parameters showed significant differences in white blood count (p = 0.005) and platelet count (p = 0.015) between patients with structural alterations and the control group. In addition, patients with structural alterations had a significantly shorter time to first treatment (TFT) (29 months) than the control group (69 months) (p = 0.037). Cases with complex karyotypes had a lower proportion of patients in Rai 0 clinical stage (15.4% vs 75%) (p = 0.005) and higher β2 microglobulin levels (3.3 vs 2.5 µg/mL) (p = 0.037) than those with simple karyotypes. Furthermore, a shorter TFT (13 months) and overall survival (56 months) in the complex karyotypes group compared with controls (69 and 144 months, respectively) (p = 0.015 and p = 0.005, respectively) were also found. Our results support the importance of cytogenetic analysis for clinical outcome in CLL and suggest that the diversity of genomic alterations is much greater than previously appreciated.

摘要

在这项研究中,我们描述了慢性淋巴细胞白血病(CLL)患者中结构性改变的细胞遗传学和荧光原位杂交(FISH)分析。结果与临床特征相关。共研究了 38 例 CLL 患者:16 例为复杂核型,22 例为简单核型。为了比较临床参数,我们还评估了一组 78 例核型正常且无 FISH 基因组改变的 CLL 患者作为对照组。我们发现了 38 种以前文献中未描述的结构性异常,其中 28 种(74%)为易位。在复杂核型病例中,染色体 6、8 和 13 是新改变中最常涉及的(各 9 个),其次是染色体 12、14 和 15(各 6 个)。染色体 8p 特别涉及缺失,8p21-pter 是最常见的重叠区域。简单核型病例中,del(6q)是最常见的改变(39%)。del(9)(q11)在我们的系列中反复出现。对临床参数的分析表明,结构性改变患者的白细胞计数(p=0.005)和血小板计数(p=0.015)与对照组有显著差异。此外,结构性改变患者的首次治疗时间(TFT)(29 个月)明显短于对照组(69 个月)(p=0.037)。复杂核型病例中 Rai 0 临床分期的患者比例较低(15.4%对 75%)(p=0.005),β2 微球蛋白水平较高(3.3 对 2.5μg/mL)(p=0.037),而简单核型病例则较低。此外,与对照组(分别为 69 个月和 144 个月)相比,复杂核型组的 TFT(13 个月)和总生存时间(56 个月)较短(p=0.015 和 p=0.005)。我们的结果支持细胞遗传学分析对 CLL 临床结果的重要性,并表明基因组改变的多样性比以前认识的要大得多。

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