TY - JOUR
T1 - A B-cell-associated gene signature classification of diffuse large B-cell lymphoma by NanoString technology
AU - Michaelsen, Thomas Yssing
AU - Richter, Julia
AU - Brøndum, Rasmus Froberg
AU - Klapper, Wolfram
AU - Johnsen, Hans Erik
AU - Albertsen, Mads
AU - Dybkær, Karen
AU - Bøgsted, Martin
N1 - This article has been found as a 'Free Version' from the Publisher on November 12th 2018. When the access to the article closes, please notify [email protected].
PY - 2018
Y1 - 2018
N2 - Gene expression profiling (GEP) by microarrays of diffuse large B-cell lymphoma (DLBCL) has enabled the categorization of DLBCL into activated B-cell-like and germinal center B-cell-like subclasses. However, as this does not fully embrace the great diversity of B-cell subtypes, we recently developed a gene expression assay for B-cell-associated gene signature (BAGS) classification. To facilitate quick and easy-to-use BAGS profiling, we developed in this study the NanoString-based BAGS2Clinic assay. Microarray data from 4 different cohorts (n = 970) were used to select genes and train the assay. The locked assay was validated in an independent cohort of 88 sample biopsies. The assay showed good correspondence with the original BAGS classifier, with an overall accuracy of 84% (95% confidence interval, 72% to 93%) and a subtype-specific accuracy ranging between 80% and 99%. BAGS classification has the potential to provide valuable insight into tumor biology as well as differences in resistance to immuno- and chemotherapy that can lead to novel treatment strategies for DLBCL patients. BAGS2Clinic can facilitate this and the implementation of BAGS classification as a routine clinical tool to improve prognosis and treatment guidance for DLBCL patients.
AB - Gene expression profiling (GEP) by microarrays of diffuse large B-cell lymphoma (DLBCL) has enabled the categorization of DLBCL into activated B-cell-like and germinal center B-cell-like subclasses. However, as this does not fully embrace the great diversity of B-cell subtypes, we recently developed a gene expression assay for B-cell-associated gene signature (BAGS) classification. To facilitate quick and easy-to-use BAGS profiling, we developed in this study the NanoString-based BAGS2Clinic assay. Microarray data from 4 different cohorts (n = 970) were used to select genes and train the assay. The locked assay was validated in an independent cohort of 88 sample biopsies. The assay showed good correspondence with the original BAGS classifier, with an overall accuracy of 84% (95% confidence interval, 72% to 93%) and a subtype-specific accuracy ranging between 80% and 99%. BAGS classification has the potential to provide valuable insight into tumor biology as well as differences in resistance to immuno- and chemotherapy that can lead to novel treatment strategies for DLBCL patients. BAGS2Clinic can facilitate this and the implementation of BAGS classification as a routine clinical tool to improve prognosis and treatment guidance for DLBCL patients.
UR - http://www.bloodadvances.org/content/bloodoa/2/13/1542.full.pdf?sso-checked=true
U2 - 10.1182/bloodadvances.2018017988
DO - 10.1182/bloodadvances.2018017988
M3 - Journal article
C2 - 29967255
SN - 2473-9529
VL - 2
SP - 1542
EP - 1546
JO - Blood advances
JF - Blood advances
IS - 13
ER -