Literature DB >> 31697802

Localized- and advanced-stage follicular lymphomas differ in their gene expression profiles.

Annette M Staiger1,2,3, Eva Hoster4, Vindi Jurinovic4, Stefan Winter2,3, Ellen Leich5,6, Claudia Kalla2,3, Peter Möller7, Heinz-Wolfram Bernd8, Alfred C Feller8, Karoline Koch9, Wolfram Klapper9, Harald Stein10, Martin-Leo Hansmann11, Sylvia Hartmann11, Martin Dreyling4, Oliver Weigert4, Wolfgang Hiddemann4, Klaus Herfarth12, Andreas Rosenwald5,6, Marianne Engelhard13, German Ott1, Heike Horn1,2,3.   

Abstract

The genetic background of follicular lymphomas (FLs) diagnosed in advanced clinical stages III/IV, and which are frequently characterized by t(14;18), has been substantially unraveled. Molecular features, as exemplified in the clinicogenetic risk model m7FLIPI, are important tools in risk stratification. In contrast, little information is available concerning localized-stage FL (clinical stages I/II), which accounts for ∼20% of newly diagnosed FL in which the detection rate of t(14;18) is only ∼50%. To investigate the genetic background of localized-stage FL, patient cohorts with advanced-stage FL or localized-stage FL, uniformly treated within phase 3 trials of the German Low-Grade Lymphoma Study Group, were comparatively analyzed. Targeted gene expression (GE) profiling of 184 genes using nCounter technology was performed in 110 localized-stage and 556 advanced-stage FL patients. By penalized Cox regression, a prognostic GE signature could not be identified in patients with advanced-stage FL, consistent with results from global tests and univariate regression. In contrast, it was possible to define robust GE signatures discriminating localized-stage and advanced-stage FL (area under the curve, 0.98) by penalized logistic regression. Of note, 3% of samples harboring an "advanced-stage signature" in the localized-stage cohort exhibited inferior failure-free survival (hazard ratio [HR], 7.1; P = .0003). Likewise, in the advanced-stage cohort, 7% of samples with a "localized-stage signature" had prolonged failure-free survival (HR, 2.3; P = .017) and overall survival (HR, 3.4; P = .072). These data support the concept of a biological difference between localized-stage and advanced-stage FL that might contribute to the superior outcome of localized FL.
© 2020 by The American Society of Hematology.

Entities:  

Mesh:

Substances:

Year:  2020        PMID: 31697802     DOI: 10.1182/blood.2019000560

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  4 in total

1.  Treatment dependence of prognostic gene expression signatures in de novo follicular lymphoma.

Authors:  Christopher R Bolen; Federico Mattiello; Michael Herold; Wolfgang Hiddemann; Sarah Huet; Wolfram Klapper; Robert Marcus; Farheen Mir; Gilles Salles; Oliver Weigert; Tina Nielsen; Mikkel Z Oestergaard; Jeffrey M Venstrom
Journal:  Blood       Date:  2021-05-13       Impact factor: 22.113

Review 2.  How we treat mature B-cell neoplasms (indolent B-cell lymphomas).

Authors:  Melissa Lumish; Lorenzo Falchi; Brandon S Imber; Michael Scordo; Gottfried von Keudell; Erel Joffe
Journal:  J Hematol Oncol       Date:  2021-01-06       Impact factor: 17.388

3.  Identification of Hub Genes and Key Pathways Associated with Follicular Lymphoma.

Authors:  Qing Zhang; Meng Wang
Journal:  Contrast Media Mol Imaging       Date:  2022-07-31       Impact factor: 3.009

4.  Molecular Cytogenetic Profiling Reveals Similarities and Differences Between Localized Nodal and Systemic Follicular Lymphomas.

Authors:  Heike Horn; Vindi Jurinovic; Ellen Leich; Sabrina Kalmbach; Julia Bausinger; Annette M Staiger; Katrin S Kurz; Peter Möller; Heinz-Wolfram Bernd; Alfred C Feller; Karoline Koch; Wolfram Klapper; Harald Stein; Martin-Leo Hansmann; Sylvia Hartmann; Gabriel Scheubeck; Martin Dreyling; Wolfgang Hiddemann; Klaus Herfarth; Marianne Engelhard; Andreas Rosenwald; Eva Hoster; German Ott
Journal:  Hemasphere       Date:  2022-08-10
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.