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Phase 2 study of cladribine followed by rituximab in patients with hairy cell leukemia.克拉屈滨序贯利妥昔单抗治疗慢性淋巴细胞白血病的Ⅱ期临床研究
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AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: prognostic implication and interaction with other gene alterations.AML1/RUNX1 突变在 470 例初发急性髓系白血病成人患者中的意义:预后影响及其与其他基因改变的相互作用。
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Genome wide molecular analysis of minimally differentiated acute myeloid leukemia.全基因组分子分析在极轻微分化型急性髓细胞白血病中的应用。
Haematologica. 2009 Nov;94(11):1546-54. doi: 10.3324/haematol.2009.009324. Epub 2009 Sep 22.
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Gene expression profiling of minimally differentiated acute myeloid leukemia: M0 is a distinct entity subdivided by RUNX1 mutation status.微分化急性髓系白血病的基因表达谱分析:M0是一个由RUNX1突变状态细分的独特实体。
Blood. 2009 Oct 1;114(14):3001-7. doi: 10.1182/blood-2009-03-211334. Epub 2009 Aug 7.
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Application of COLD-PCR for improved detection of KRAS mutations in clinical samples.应用COLD-PCR改进临床样本中KRAS突变的检测
Mod Pathol. 2009 Aug;22(8):1023-31. doi: 10.1038/modpathol.2009.59. Epub 2009 May 8.
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Molecular pathways mediating MDS/AML with focus on AML1/RUNX1 point mutations.介导骨髓增生异常综合征/急性髓系白血病的分子途径,重点关注AML1/RUNX1点突变
J Cell Physiol. 2009 Jul;220(1):16-20. doi: 10.1002/jcp.21769.
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Cell cycle and developmental control of hematopoiesis by Runx1.Runx1对造血作用的细胞周期及发育调控
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8
Trisomy 13 correlates with RUNX1 mutation and increased FLT3 expression in AML-M0 patients.13三体与急性髓系白血病微分化型(AML-M0)患者的RUNX1突变及FLT3表达增加相关。
Haematologica. 2007 Aug;92(8):1123-6. doi: 10.3324/haematol.11296.
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Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia.13三体与急性髓系白血病中的AML1/RUNX1突变及FLT3表达增加密切相关。
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10
Activating FLT3 mutations are detectable in chronic and blast phase of chronic myeloproliferative disorders other than chronic myeloid leukemia.除慢性髓性白血病外,在慢性髓性增殖性疾病的慢性期和急变期可检测到激活型FLT3突变。
Am J Clin Pathol. 2006 Oct;126(4):530-3. doi: 10.1309/JT5BE2L1FGG8P8Y6.

TdT 表达在极轻微分化的急性髓细胞白血病中与独特的临床病理特征相关,并在干细胞移植后具有更好的总生存。

TdT expression in acute myeloid leukemia with minimal differentiation is associated with distinctive clinicopathological features and better overall survival following stem cell transplantation.

机构信息

Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Mod Pathol. 2013 Feb;26(2):195-203. doi: 10.1038/modpathol.2012.142. Epub 2012 Aug 31.

DOI:10.1038/modpathol.2012.142
PMID:22936064
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5485410/
Abstract

The diagnostic criteria for acute myeloid leukemia (AML), not otherwise specified, with minimal differentiation (AML-M0, French-American-British classification), have been refined in the 2008 World Health Organization (WHO) classification. Terminal deoxynucleotidyl transferase (TdT) expression in AML-M0 has been proposed by others as a surrogate for RUNX1 (runt-related transcription factor 1) mutations, a mutation associated with distinct gene expression profiles in AML-M0. In this study, we investigated the significance of TdT expression in AML-M0 cases defined using the 2008 WHO classification criteria. Demographic, laboratory and clinical information were obtained from the hospital medical records. Statistical analysis was performed using Student's t-test, log-rank test and Fisher's exact test. The study group included 30 AML-M0 patients (male:female=19:11; median age: 60 years). In all, 10 cases of AML-M0 were positive for TdT(+) and 20 cases were negative for TdT(-). Patients with TdT+ AML-M0 had higher peripheral blood and bone marrow blast counts compared to patients with TdT- AML-M0 (P=0.01). TdT expression in AML-M0 was not associated with a distinct immunophenotype. Monoclonal IgH and TCR gene rearrangements were frequent, but independent of TdT expression in AML-M0. TdT expression in AML-M0 correlated with trisomy 13 and inversely correlated with aberrations of chromosomes 5 and 17. Among six patients with AML-M0 who received a stem cell transplant, overall survival was significantly longer for the three TdT+ patients compared with the three TdT- patients (P=0.03). In the TdT+AML-M0 subgroup, the three patients with stem cell transplant had better overall survival compared with five patients who did not receive stem cell transplant (P=0.01). We conclude that AML-M0, as currently defined in the 2008 WHO classification, can be divided into two groups based on TdT expression. Although there is a need to assess a greater number of patients, our results suggest that TdT positivity in AML-M0 identifies a subset of patients with a better prognosis after stem cell transplant.

摘要

未分化型急性髓细胞白血病(AML,不另作分类)的诊断标准,在 2008 年世界卫生组织(WHO)分类中已经得到了细化。端粒酶(TdT)在 AML-M0 中的表达已被其他学者提出作为 RUNX1(runt 相关转录因子 1)突变的替代物,而 RUNX1 突变与 AML-M0 中独特的基因表达谱相关。在这项研究中,我们研究了 2008 年 WHO 分类标准定义的 AML-M0 病例中 TdT 表达的意义。从医院病历中获得人口统计学、实验室和临床信息。使用学生 t 检验、对数秩检验和 Fisher 精确检验进行统计分析。研究组包括 30 例 AML-M0 患者(男:女=19:11;中位年龄:60 岁)。其中 10 例 AML-M0 为 TdT(+),20 例为 TdT(-)。TdT+AML-M0 患者的外周血和骨髓原始细胞计数高于 TdT-AML-M0 患者(P=0.01)。TdT 在 AML-M0 中的表达与独特的免疫表型无关。单克隆 IgH 和 TCR 基因重排很常见,但与 AML-M0 中的 TdT 表达无关。TdT 在 AML-M0 中的表达与三体 13 相关,与染色体 5 和 17 的异常呈负相关。在接受干细胞移植的 6 例 AML-M0 患者中,3 例 TdT+患者的总生存率明显长于 3 例 TdT-患者(P=0.03)。在 TdT+AML-M0 亚组中,与未接受干细胞移植的 5 例患者相比,3 例接受干细胞移植的患者的总生存率更好(P=0.01)。我们得出结论,根据 TdT 表达,目前在 2008 年 WHO 分类中定义的 AML-M0 可以分为两组。尽管需要评估更多的患者,但我们的结果表明,AML-M0 中的 TdT 阳性可识别出一组在干细胞移植后预后更好的患者。