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信号转导和转录激活因子3(STAT3)突变在伴有纯红细胞再生障碍性贫血的T细胞大颗粒淋巴细胞白血病中很常见。

STAT3 mutations are frequent in T-cell large granular lymphocytic leukemia with pure red cell aplasia.

作者信息

Qiu Zhi-Yuan, Fan Lei, Wang Li, Qiao Chun, Wu Yu-Jie, Zhou Jian-Feng, Xu Wei, Li Jian-Yong

出版信息

J Hematol Oncol. 2013 Oct 31;6:82. doi: 10.1186/1756-8722-6-82.

Abstract

T-cell large granular lymphocytic leukemia (T-LGLL) is a rare lymphoproliferative disorder and can cooccur in the context of pure red cell aplasia (PRCA). The aim of the current study was to analyze the signal transducer and activator of transcription 3 (STAT3) mutation status and its clinical significance in T-LGLL. We found STAT3 mutations in 21.4% of patients with T-LGLL. High ß2-MG (ß2-microglobulin) levels (P = 0.005), neutropenia (P = 0.018) and PRCA (P = 0.001) all displayed a significant association with STAT3 mutations. In univariate analysis, treatment-free survival (TFS) was affected by STAT3 mutation status (P=0.008) and ß2-MG (P = 0.006). Our results demonstrate the remarkable correlation of STAT3 mutation with PRCA, neutropenia and ß2-MG.

摘要

T细胞大颗粒淋巴细胞白血病(T-LGLL)是一种罕见的淋巴细胞增殖性疾病,可与纯红细胞再生障碍性贫血(PRCA)同时出现。本研究的目的是分析信号转导和转录激活因子3(STAT3)突变状态及其在T-LGLL中的临床意义。我们发现21.4%的T-LGLL患者存在STAT3突变。高β2-微球蛋白(β2-MG)水平(P = 0.005)、中性粒细胞减少(P = 0.018)和PRCA(P = 0.001)均与STAT3突变显著相关。在单因素分析中,无治疗生存期(TFS)受STAT3突变状态(P = 0.008)和β2-MG(P = 0.006)影响。我们的结果表明STAT3突变与PRCA、中性粒细胞减少和β2-MG显著相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f49/4222121/65a89903a921/1756-8722-6-82-1.jpg

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