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Individual patient risk stratification of high-risk neuroblastomas using a two-gene score suited for clinical use.
von Stedingk, Kristoffer; De Preter, Katleen; Vandesompele, Jo; Noguera, Rosa; Øra, Ingrid; Koster, Jan; Versteeg, Rogier; Påhlman, Sven; Lindgren, David; Axelson, Håkan.
Afiliación
  • von Stedingk K; Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
  • De Preter K; Department of Pediatric Oncology and Hematology, Skåne University Hospital, Lund University, Lund, Sweden.
  • Vandesompele J; Center for Medical Genetics, Department of Pediatrics and Genetics, Ghent University, Ghent, Belgium.
  • Noguera R; Center for Medical Genetics, Department of Pediatrics and Genetics, Ghent University, Ghent, Belgium.
  • Øra I; Department of Pathology, Medical School, University of Valencia, Valencia, Spain.
  • Koster J; Department of Pediatric Oncology and Hematology, Skåne University Hospital, Lund University, Lund, Sweden.
  • Versteeg R; Department of Oncogenomics, Academic Medical Center, Amsterdam, The Netherlands.
  • Påhlman S; Department of Oncogenomics, Academic Medical Center, Amsterdam, The Netherlands.
  • Lindgren D; Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
  • Axelson H; Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Int J Cancer ; 137(4): 868-77, 2015 Aug 15.
Article en En | MEDLINE | ID: mdl-25652004
ABSTRACT
Several gene expression-based prognostic signatures have been described in neuroblastoma, but none have successfully been applied in the clinic. Here we have developed a clinically applicable prognostic gene signature, both with regards to number of genes and analysis platform. Importantly, it does not require comparison between patients and is applicable amongst high-risk patients. The signature is based on a two-gene score (R-score) with prognostic power in high-stage tumours (stage 4 and/or MYCN-amplified diagnosed after 18 months of age). QPCR-based and array-based analyses of matched cDNAs confirmed cross platform (array-qPCR) transferability. We also defined a fixed cut-off value identifying prognostically differing subsets of high-risk patients on an individual patient basis. This gene expression signature independently contributes to the current neuroblastoma classification system, and if prospectively validated could provide further stratification of high-risk patients, and potential upfront identification of a group of patients that are in need of new/additional treatment regimens.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Detección Precoz del Cáncer / Transcriptoma / Proteínas de Neoplasias / Neuroblastoma Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Child, preschool / Humans / Infant Idioma: En Revista: Int J Cancer Año: 2015 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Detección Precoz del Cáncer / Transcriptoma / Proteínas de Neoplasias / Neuroblastoma Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Child, preschool / Humans / Infant Idioma: En Revista: Int J Cancer Año: 2015 Tipo del documento: Article País de afiliación: Suecia