TY - JOUR
T1 - Discordant cell-of-origin in refractory/relapsed LBCL at diagnosis and relapse
AU - Riber Hansen, Elisabeth Victoria
AU - Dennis, Shannon
AU - Brændstrup, Peter
AU - Eriksen, Jens Ole
AU - Everhøj, Anja Elaine
AU - Litman, Thomas
AU - Pedersen, Lars Møller
AU - Pedersen, Mette Ølgod
AU - Gjerdrum, Lise Mette Rahbek
PY - 2026/1
Y1 - 2026/1
N2 - Gene expression profiling (GEP)-based cell-of-origin (COO) classification is the gold standard for molecular subtyping of diffuse large B-cell lymphoma (DLBCL). However, the consistency of COO classification over time, particularly in relapsed or refractory (R/R) settings, remains insufficiently validated. In this longitudinal study, we assessed the stability and reproducibility of COO classification using the NanoString Lymph2Cx assay in paired primary and relapse samples from 84 patients with R/R LBCL. Of these, 90.2% were classified as either activated B-cell-like (ABC) or germinal center B-cell-like (GCB). COO inconsistencies were observed in 18 patients, with four patients showing a shift between ABC and GCB subtypes. While the Lymph2Cx assay demonstrates utility in COO determination, our findings raise important questions regarding the biological and clinical implications of COO shifts. Further investigation is needed to understand the mechanisms behind this instability and to refine the role of COO assessment in guiding therapeutic strategies for R/R LBCL.
AB - Gene expression profiling (GEP)-based cell-of-origin (COO) classification is the gold standard for molecular subtyping of diffuse large B-cell lymphoma (DLBCL). However, the consistency of COO classification over time, particularly in relapsed or refractory (R/R) settings, remains insufficiently validated. In this longitudinal study, we assessed the stability and reproducibility of COO classification using the NanoString Lymph2Cx assay in paired primary and relapse samples from 84 patients with R/R LBCL. Of these, 90.2% were classified as either activated B-cell-like (ABC) or germinal center B-cell-like (GCB). COO inconsistencies were observed in 18 patients, with four patients showing a shift between ABC and GCB subtypes. While the Lymph2Cx assay demonstrates utility in COO determination, our findings raise important questions regarding the biological and clinical implications of COO shifts. Further investigation is needed to understand the mechanisms behind this instability and to refine the role of COO assessment in guiding therapeutic strategies for R/R LBCL.
KW - gene expression profiling
KW - large B-cell lymphoma
KW - Lymphoid neoplasia
U2 - 10.1080/10428194.2025.2594052
DO - 10.1080/10428194.2025.2594052
M3 - Journal article
C2 - 41334687
AN - SCOPUS:105023846961
SN - 1042-8194
VL - 67
SP - 377
EP - 384
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 2
ER -