Dai Chengguqiu, Chen Mengya, Wang Chaolong, Hao Xingjie
Department of Epidemiology and Biostatistics, Key Laboratory for Environment and Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Front Cell Dev Biol. 2021 Nov 12;9:762260. doi: 10.3389/fcell.2021.762260. eCollection 2021.
Acute myeloid leukemia (AML) is one of the malignant hematologic cancers with rapid progress and poor prognosis. Most AML prognostic stratifications focused on genetic abnormalities. However, none of them was established based on the cell type compositions (CTCs) of peripheral blood or bone marrow aspirates from patients at diagnosis. Here we sought to develop a novel prognostic model for AML in adults based on the CTCs. First, we applied the CIBERSORT algorithm to estimate the CTCs for patients from two public datasets (GSE6891 and TCGA-LAML) using a custom gene expression signature reference constructed by an AML single-cell RNA sequencing dataset (GSE116256). Then, a CTC-based prognostic model was established using least absolute shrinkage and selection operator Cox regression, termed CTC score. The constructed prognostic model CTC score comprised 3 cell types, GMP-like, HSC-like, and T. Compared with the low-CTC-score group, the high-CTC-score group showed a 1.57-fold [95% confidence interval (CI), 1.23 to 2.00; = 0.0002] and a 2.32-fold (95% CI, 1.53 to 3.51; 0.0001) higher overall mortality risk in the training set (GSE6891) and validation set (TCGA-LAML), respectively. When adjusting for age at diagnosis, cytogenetic risk, and karyotype, the CTC score remained statistically significant in both the training set [hazard ratio (HR) = 2.25; 95% CI, 1.20 to 4.24; = 0.0119] and the validation set (HR = 7.97; 95% CI, 2.95 to 21.56; 0.0001]. We further compared the performance of the CTC score with two gene expression-based prognostic scores: the 17-gene leukemic stem cell score (LSC17 score) and the AML prognostic score (APS). It turned out that the CTC score achieved comparable performance at 1-, 2-, 3-, and 5-years timepoints and provided independent and additional prognostic information different from the LSC17 score and APS. In conclusion, the CTC score could serve as a powerful prognostic marker for AML and has great potential to assist clinicians to formulate individualized treatment plans.
急性髓系白血病(AML)是进展迅速且预后较差的恶性血液系统癌症之一。大多数AML预后分层聚焦于基因异常。然而,这些分层均未基于诊断时患者外周血或骨髓穿刺液的细胞类型组成(CTC)而建立。在此,我们试图基于CTC开发一种针对成人AML的新型预后模型。首先,我们应用CIBERSORT算法,使用由AML单细胞RNA测序数据集(GSE116256)构建的自定义基因表达特征参考,来估计来自两个公共数据集(GSE6891和TCGA-LAML)患者的CTC。然后,使用最小绝对收缩和选择算子Cox回归建立基于CTC的预后模型,称为CTC评分。构建的预后模型CTC评分包含3种细胞类型,即类GMP、类HSC和T细胞。与低CTC评分组相比,高CTC评分组在训练集(GSE6891)和验证集(TCGA-LAML)中的总死亡风险分别高1.57倍[95%置信区间(CI),1.23至2.00;P = 0.0002]和2.32倍(95%CI,1.53至3.51;P = 0.0001)。在调整诊断时的年龄、细胞遗传学风险和核型后,CTC评分在训练集[风险比(HR)= 2.25;95%CI,1.20至4.24;P = 0.0119]和验证集(HR = 7.97;95%CI,2.95至21.56;P = 0.0001)中仍具有统计学意义。我们进一步将CTC评分的性能与两个基于基因表达的预后评分进行比较:17基因白血病干细胞评分(LSC17评分)和AML预后评分(APS)。结果表明,CTC评分在1年、2年、3年和5年时间点具有相当的性能,并提供了与LSC17评分和APS不同的独立且额外的预后信息。总之,CTC评分可作为AML的有力预后标志物,在协助临床医生制定个体化治疗方案方面具有巨大潜力。