Immunohistochemical Classification and Prognostic Significance of Germinal Center-like and Memory Cell-like Subtypes of Follicular Lymphoma Using FOXP1, LMO2, CD22, and MUM1
Sep 2026· International Journal of Molecular Sciences· Vol 27, pp. 8611· 0 citations· 14 references
Medicine
TL;DR
It is suggested that LMO2 and FOXP1 expression may provide complementary prognostic information and help identify clinically distinct immunophenotypic subsets in FL.
Abstract
Follicular lymphoma (FL) is an indolent B-cell lymphoma with considerable biological and clinical heterogeneity, highlighting the need for additional prognostic biomarkers beyond conventional clinicopathological parameters. This study aimed to evaluate the prognostic significance of an immunohistochemical classification separating FL into a germinal center-like (GC-like) phenotype, characterized by retention of germinal-center-associated features, and a memory-like (Mem-like) phenotype, reflecting a more differentiated post-germinal-center/memory B-cell state. Fifty-one patients with FL were retrospectively analyzed for clinicopathological characteristics, immunohistochemical findings, relapse, and overall survival (OS). LMO2 expression was detected in 70.6% of cases and was associated with lower mortality (19.4% vs. 60.0%, p = 0.008), lower relapse rates (8.3% vs. 33.3%, p = 0.039), and improved 5-year OS (85.3% vs. 35.0%, log-rank p = 0.003). FOXP1 positivity was observed in 41.2% of cases and was associated with higher mortality (57.1% vs. 13.3%, p = 0.002) and inferior 5-year OS (44.5% vs. 89.4%, log-rank p < 0.001). Mem-like patients had significantly poorer 5-year OS than GC-like patients (39.5% vs. 90.1%, log-rank p < 0.001). These findings suggest that LMO2 and FOXP1 expression may provide complementary prognostic information and help identify clinically distinct immunophenotypic subsets in FL.
Mantle cell lymphoma (MCL) is a rare mature B-cell non-Hodgkin lymphoma that is known to exhibit heterogeneous biological behavior and variable clinical outcomes. Ki-67 proliferation index, blastoid morphology, and p53 expression are important prognostic markers.
The primary objective was to analyze the cl...
Jameera Nazer, Indu R. Nair, Wesley Jose· Cancer Research, Statistics,...· 0 citations
Background: Programmed death-ligand 1 (PD-L1) contributes to immune escape and is a therapeutically relevant target in aggressive B-cell lymphomas. However, its distribution and clinicopathologic significance across primary mediastinal aggressive large B-cell lymphomas remain incompletely defined. Methods: We retrospec...
Serhat Kaymaz, Selçuk Cin, T. Elverdi et al.· Diagnostics· 0 citations
We evaluated morphologic and immunophenotypic features of adult T-cell leukemia/lymphoma (ATLL) using morphology and flow cytometry (FCM), compared tumor cell proportions in bone marrow (BM) and peripheral blood (PB), and assessed whether these parameters could improve prognostication beyond existing indices for aggres...
Feng Zhang, Hua-Rong Zhou, Fei Gao et al.· Cytometry. Part B, Clinical...· 0 citations
Diffuse large B-cell lymphoma (DLBCL) is an aggressive lymphoma that accounts for many B-cell lymphomas. The molecular heterogeneity of DLBCL has been increasingly recognized on the different biological origins and varying clinical manifestations and treatment responses of this disease which makes the DLBCL an extremel...
Sahil Panjvani, B. Kar· IFR Journal of Medical Scien...· 0 citations
Background: Diffuse large B-cell lymphoma (DLBCL) is the most common subtype of non-Hodgkin lymphoma (NHL), characterized by clinical and molecular heterogeneity. Genetic alterations in signaling pathways, especially the MYD88 gene, have been implicated in disease progression and prognosis. Although MYD88 protein expre...
Wanlapa Rattanasawat, Wasakorn Bunyayothin, Sirisanpang Yodavudh· Journal of the Medical Assoc...· 0 citations