首页> 外文期刊>Hematological oncology >Del(13q14.3) length matters: An integrated analysis of genomic, fluorescence in situ hybridization and clinical data in 169 chronic lymphocytic leukaemia patients with 13q deletion alone or a normal karyotype
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Del(13q14.3) length matters: An integrated analysis of genomic, fluorescence in situ hybridization and clinical data in 169 chronic lymphocytic leukaemia patients with 13q deletion alone or a normal karyotype

机译:Del(13q14.3)长度很重要:对169例仅具有13q缺失或正常核型的慢性淋巴细胞性白血病患者的基因组,荧光原位杂交和临床数据的综合分析

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Chronic lymphocytic leukaemia (CLL), characterizedby a monoclonal expansion and accumulation of smallmature B lymphocytes, is the most common adult‐onsetleukaemia in the Western world [1,2]. The disease has avery heterogenous natural clinical course, and survivalafter diagnosis can range from months to decades [1–3].The most frequent chromosomal aberration is del(13q14.3), which occurs in about 50% of cases and targetsthe DLEU2/MIR15A/MIR16B locus [4–6]. Deletions at13q14.3 vary in size, and the involvement of transcriptsother than MIR15A/MIR16B has been proposed [7–10].The clinical relevance of the larger 13q14.3 deletions isnot well established. Amongst 179 CLL patients [74 withdel(13q14.3)], Ouillette et al. [7] reported an associationbetween poorer clinical features and larger deletions, butno data were presented on overall survival (OS) or time totreatment (TT).
机译:慢性淋巴细胞性白血病(CLL)以小B淋巴细胞的单克隆扩增和积累为特征,是西方世界最常见的成人发作性白血病[1,2]。该疾病具有不同的自然自然临床病程,诊断后的生存期从数月到数十年不等[1-3]。最常见的染色体畸变是del(13q14.3),约50%的病例发生,以DLEU2 / MIR15A为靶点/ MIR16B基因座[4-6]。 13q14.3缺失的大小不一,已经提出了涉及MIR15A / MIR16B以外的转录物的参与[7-10]。较大的13q14.3缺失的临床相关性尚不明确。在179名CLL患者中[74 withdel(13q14.3)],Ouillette等人。 [7]报道了较差的临床特征和较大的缺失之间的关联,但是没有关于总生存期(OS)或治疗时间(TT)的数据。

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