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CLLU1 表达在一线治疗后年轻患者和 IGHV 基因突变的慢性淋巴细胞白血病患者中有预后价值。

CLLU1 expression has prognostic value in chronic lymphocytic leukemia after first-line therapy in younger patients and in those with mutated IGHV genes.

机构信息

Haemato-Oncology Research Unit, Division of Molecular Pathology, The Institute of Cancer Research, London, UK.

出版信息

Haematologica. 2013 Feb;98(2):274-8. doi: 10.3324/haematol.2012.070201. Epub 2012 Aug 16.

DOI:10.3324/haematol.2012.070201
PMID:22899580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3561436/
Abstract

CLLU1, located at chromosome 12q22, encodes a transcript specific to chronic lymphocytic leukemia and has potential prognostic value. We assessed the value of CLLU1 expression in the LRF CLL4 randomized trial. Samples from 515 patients with chronic lymphocytic leukemia were collected immediately before the start of treatment. After RNA extraction and cDNA synthesis, CLLU1 expression was assessed by quantitative polymerase chain reaction. In total, 247 and 268 samples were identified as having low and high CLLU1 expression, respectively. The median follow-up was 88 months. High CLLU1 expression was significantly correlated with unmutated IGHV genes, ZAP-70 and CD38 positivity, and absence of 13q deletion (all r>0.2, P<0.0001). At 6 years, patients with high CLLU1 expression had significantly worse progression-free survival (9% versus 17%; P=0.03) and overall survival (42% versus 57%; P=0.0003) than patients with low CLLU1 expression. Among patients with mutated IGHV genes, overall survival at 6 years was 50% in those with high CLLU1 expression and 76% in those with low CLLU1 expression (P=0.005). However, CLLU1 expression was not an independent predictor of overall survival in a multivariate model including TP53 aberrations, beta-2 microglobulin level, age and IGHV mutation status. Nor did it predict response to treatment. CLLU1 expression analysis helps to refine the prognosis of patients with chronic lymphocytic leukemia who have mutated IGHV genes.

摘要

CLLU1 位于染色体 12q22,编码一种特异性表达于慢性淋巴细胞白血病的转录本,具有潜在的预后价值。我们评估了 CLLU1 表达在 LRF CLL4 随机试验中的价值。在开始治疗前,采集了 515 例慢性淋巴细胞白血病患者的样本。提取 RNA 并合成 cDNA 后,通过定量聚合酶链反应评估 CLLU1 的表达。共有 247 例和 268 例样本分别被鉴定为低表达和高表达 CLLU1。中位随访时间为 88 个月。高 CLLU1 表达与未突变的 IGHV 基因、ZAP-70 和 CD38 阳性以及 13q 缺失缺失显著相关(均 r>0.2,P<0.0001)。6 年后,高 CLLU1 表达的患者无进展生存期(9%比 17%;P=0.03)和总生存期(42%比 57%;P=0.0003)显著低于低 CLLU1 表达的患者。在 IGHV 基因突变的患者中,高 CLLU1 表达患者的 6 年总生存率为 50%,而低 CLLU1 表达患者的 6 年总生存率为 76%(P=0.005)。然而,在包括 TP53 异常、β-2 微球蛋白水平、年龄和 IGHV 突变状态在内的多变量模型中,CLLU1 表达并不是总生存期的独立预测因素。它也不能预测治疗反应。CLLU1 表达分析有助于改善 IGHV 基因突变的慢性淋巴细胞白血病患者的预后。

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