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Identification of a miRNA based model to detect prognostic subgroups in patients with aggressive B-cell lymphoma.
Nordmo, Carmen; Glehr, Gunther; Altenbuchinger, Michael; Spang, Rainer; Ziepert, Marita; Horn, Heike; Staiger, Annette M; Ott, German; Schmitz, Norbert; Held, Gerhard; Einsele, Hermann; Topp, Max; Rosenwald, Andreas; Rauert-Wunderlich, Hilka.
  • Nordmo C; Department of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany.
  • Glehr G; Institute of Pathology, University of Würzburg and Comprehensive Cancer Center (CCC) Mainfranken, Würzburg, Germany.
  • Altenbuchinger M; Institute of Functional Genomics, Statistical Bioinformatics, University of Regensburg, Regensburg, Germany.
  • Spang R; Institute of Functional Genomics, Statistical Bioinformatics, University of Regensburg, Regensburg, Germany.
  • Ziepert M; Institute of Functional Genomics, Statistical Bioinformatics, University of Regensburg, Regensburg, Germany.
  • Horn H; Institute of Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.
  • Staiger AM; Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology, Stuttgart, Germany and University of Tuebingen, Tuebingen, Germany.
  • Ott G; Department of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart, Germany.
  • Schmitz N; Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology, Stuttgart, Germany and University of Tuebingen, Tuebingen, Germany.
  • Held G; Department of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart, Germany.
  • Einsele H; Department of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart, Germany.
  • Topp M; Department of Medicine A, University Hospital Münster, Münster, Germany.
  • Rosenwald A; DSHNHL Studiensekretariat, Westpfalz Klinikum GmbH, Kaiserslautern, Germany.
  • Rauert-Wunderlich H; Department of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany.
Leuk Lymphoma ; 62(5): 1107-1115, 2021 05.
Article en En | MEDLINE | ID: mdl-33353431
ABSTRACT
In order to differentiate prognostic subgroups of patients with aggressive B-cell lymphoma, we analyzed the expression of 800 miRNAs with the NanoString nCounter human miRNA assay on a cohort of 228 FFPE samples of patients enrolled in the RICOVER-60 and MegaCHOEP trials. We identified significant miRNA signatures for overall survival (OS) and progression-free survival (PFS) by LASSO-penalized linear Cox-regression. High expression levels of miR-130a-3p and miR-423-5p indicate a better prognosis, whereas high levels of miR-374b-5p, miR-590-5p, miR-186-5p, and miR-106b-5p increase patients' risk levels for OS. Regarding PFS high expression of miR-365a-5p in addition to the other two miRNAs improves the prognosis and high levels of miR374a-5p, miR-106b-5p, and miR-590-5p, connects with increased risk and poor prognosis. We identified miRNA signatures to subdivide patients into two different risk groups. These prognostic models may be used in risk stratification in future clinical trials and help making personalized therapy decisions.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Linfoma de Células B / MicroARNs Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Linfoma de Células B / MicroARNs Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article