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基于微环境中慢性淋巴细胞白血病激活的基因表达谱分析预测疾病进展。

A gene expression assay based on chronic lymphocytic leukemia activation in the microenvironment to predict progression.

机构信息

Servei d'Hematologia, Vall d'Hebron Hospital Universitari, Experimental Hematology, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.

Departament de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain.

出版信息

Blood Adv. 2022 Nov 8;6(21):5763-5773. doi: 10.1182/bloodadvances.2022007508.

DOI:10.1182/bloodadvances.2022007508
PMID:35973197
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9647836/
Abstract

Several gene expression profiles with a strong correlation with patient outcomes have been previously described in chronic lymphocytic leukemia (CLL), although their applicability as biomarkers in clinical practice has been particularly limited. Here we describe the training and validation of a gene expression signature for predicting early progression in patients with CLL based on the analysis of 200 genes related to microenvironment signaling on the NanoString platform. In the training cohort (n = 154), the CLL15 assay containing a 15-gene signature was associated with the time to first treatment (TtFT) (hazard ratio [HR], 2.83; 95% CI, 2.17-3.68; P < .001). The prognostic value of the CLL15 score (HR, 1.71; 95% CI, 1.15-2.52; P = .007) was further confirmed in an external independent validation cohort (n = 112). Notably, the CLL15 score improved the prognostic capacity over IGHV mutational status and the International Prognostic Score for asymptomatic early-stage (IPS-E) CLL. In multivariate analysis, the CLL15 score (HR, 1.83; 95% CI, 1.32-2.56; P < .001) and the IPS-E CLL (HR, 2.23; 95% CI, 1.59-3.12; P < .001) were independently associated with TtFT. The newly developed and validated CLL15 assay successfully translated previous gene signatures such as the microenvironment signaling into a new gene expression-based assay with prognostic implications in CLL.

摘要

先前已经描述了几种与慢性淋巴细胞白血病(CLL)患者结局密切相关的基因表达谱,但它们作为临床实践中的生物标志物的适用性尤其有限。在这里,我们描述了一种基于 NanoString 平台分析与微环境信号相关的 200 个基因的基因表达谱,用于预测 CLL 患者早期进展的训练和验证。在训练队列(n=154)中,包含 15 个基因特征的 CLL15 检测与首次治疗时间(TtFT)相关(风险比[HR],2.83;95%置信区间[CI],2.17-3.68;P<0.001)。CLL15 评分(HR,1.71;95%CI,1.15-2.52;P=0.007)的预后价值在外部独立验证队列(n=112)中得到进一步证实。值得注意的是,CLL15 评分提高了 IGHV 突变状态和无症状早期(IPS-E)CLL 的国际预后评分(IPS-E)的预后能力。在多变量分析中,CLL15 评分(HR,1.83;95%CI,1.32-2.56;P<0.001)和 IPS-E CLL(HR,2.23;95%CI,1.59-3.12;P<0.001)与 TtFT 独立相关。新开发和验证的 CLL15 检测成功地将先前的基因特征(如微环境信号)转化为一种新的基于基因表达的检测方法,该方法对 CLL 具有预后意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/9647836/3b0a80711719/BLOODA_ADV-2022-007508-gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/9647836/8a74491213b2/BLOODA_ADV-2022-007508-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/9647836/a9883487051f/BLOODA_ADV-2022-007508-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/9647836/d895fa123bbf/BLOODA_ADV-2022-007508-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/9647836/cfaa41bc2fc8/BLOODA_ADV-2022-007508-gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/9647836/3b0a80711719/BLOODA_ADV-2022-007508-gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/9647836/8a74491213b2/BLOODA_ADV-2022-007508-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/9647836/a9883487051f/BLOODA_ADV-2022-007508-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/9647836/d895fa123bbf/BLOODA_ADV-2022-007508-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/9647836/cfaa41bc2fc8/BLOODA_ADV-2022-007508-gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e755/9647836/3b0a80711719/BLOODA_ADV-2022-007508-gr5.jpg

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