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

Authors :
Asociación Española Contra el Cáncer
Instituto de Salud Carlos III
Ministerio de Economía y Competitividad (España)
Junta de Castilla y León
Fundació La Marató de TV3
Abrisqueta, Pau
Medina, Daniel
Villacampa, Guillermo
Lu, Junyan
Alcoceba, Miguel
Carabia, Julia
Boix, Joan
Tazón‐Vega, Bárbara
Iacoboni, Gloria
Bobillo, Sabela
Marín-Niebla, Ana
González, Marcos
Zenz, Thorsten
Crespo, Marta
Bosch, Francesc
Asociación Española Contra el Cáncer
Instituto de Salud Carlos III
Ministerio de Economía y Competitividad (España)
Junta de Castilla y León
Fundació La Marató de TV3
Abrisqueta, Pau
Medina, Daniel
Villacampa, Guillermo
Lu, Junyan
Alcoceba, Miguel
Carabia, Julia
Boix, Joan
Tazón‐Vega, Bárbara
Iacoboni, Gloria
Bobillo, Sabela
Marín-Niebla, Ana
González, Marcos
Zenz, Thorsten
Crespo, Marta
Bosch, Francesc
Publication Year :
2022

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.

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1373159578
Document Type :
Electronic Resource