Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Mod Pathol. 2013 Feb;26(2):195-203. doi: 10.1038/modpathol.2012.142. Epub 2012 Aug 31.
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.
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。