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T 细胞急性淋巴细胞白血病中 PTEN 异常的与年龄相关的临床和生物学特征。

Age-related clinical and biological features of PTEN abnormalities in T-cell acute lymphoblastic leukaemia.

机构信息

Institut Necker-Enfants Malades (INEM), Institut national de recherche médicale (INSERM) U1151, Hôpital Necker-Enfants Malades, Paris, France.

Université Paris Descartes Sorbonne Cité and Laboratory of Onco-Hematology, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Necker-Enfants Malades, Paris, France.

出版信息

Leukemia. 2017 Dec;31(12):2594-2600. doi: 10.1038/leu.2017.157. Epub 2017 May 25.

DOI:10.1038/leu.2017.157
PMID:28539671
Abstract

The tumour suppressor gene PTEN is commonly altered in T-cell acute lymphoblastic leukaemia but its prognostic impact is still debated. We screened a cohort of 573 fully characterised adult and paediatric T-cell acute lymphoblastic leukaemia (T-ALL) patients for genomic PTEN abnormalities. PTEN-inactivating mutations and/or deletions were identified in 91 cases (16%), including 18% of paediatric (49/277) and 14% of adult cases (42/296). Thirty-four patients harboured only mutations, 12 cases demonstrated only large deletions and 9 only microdeletions. About 36 patients had combined alterations. Different mechanisms of PTEN inactivation predicted differences in the clinical outcome for both adult and paediatric patients treated according to the GRAALL03/05 and FRALLE2000 protocols. Whereas large deletions predicted lower 5-year overall survival (P=0.0053 in adults, P=0.001 in children) and disease-free survival (P=0.0009 in adults, P=0.0002 in children), mutations were not associated with a worse prognosis. The prognostic impact of PTEN loss is therefore linked to the underlying type of genomic abnormality, both in adult and paediatric T-ALLs, demonstrating that detailed analysis of the type of abnormality type would be useful to refine risk stratification.

摘要

抑癌基因 PTEN 通常在 T 细胞急性淋巴细胞白血病中发生改变,但它的预后影响仍存在争议。我们对 573 例经过充分特征描述的成人和儿童 T 细胞急性淋巴细胞白血病(T-ALL)患者进行了基因组 PTEN 异常筛选。在 91 例(16%)患者中发现了 PTEN 失活突变和/或缺失,包括 18%的儿科病例(49/277)和 14%的成人病例(42/296)。34 例患者仅存在突变,12 例仅存在大片段缺失,9 例仅存在微小缺失。约 36 例患者存在联合改变。PTEN 失活的不同机制预测了根据 GRAALL03/05 和 FRALLE2000 方案治疗的成人和儿科患者的临床结局存在差异。而大片段缺失预测了较低的 5 年总生存率(成人 P=0.0053,儿童 P=0.001)和无病生存率(成人 P=0.0009,儿童 P=0.0002),而突变与预后不良无关。因此,PTEN 缺失的预后影响与成人和儿童 T-ALL 中潜在的基因组异常类型有关,这表明详细分析异常类型将有助于细化风险分层。

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