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Frequency and clinical correlates of elevated plasma Epstein-Barr virus DNA at diagnosis in peripheral T-cell lymphomas.
Haverkos, Bradley M; Huang, Ying; Gru, Alejandro; Pancholi, Preeti; Freud, Aharon G; Mishra, Anjali; Ruppert, Amy S; Baiocchi, Robert A; Porcu, Pierluigi.
Afiliação
  • Haverkos BM; Division of Hematology, University of Colorado, Aurora, CO.
  • Huang Y; Division of Hematology, The Ohio State University, Columbus, OH.
  • Gru A; Department of Pathology, University of Virginia, Charlottesville, VA.
  • Pancholi P; Department of Pathology, The Ohio State University, Columbus, OH.
  • Freud AG; Department of Pathology, The Ohio State University, Columbus, OH.
  • Mishra A; Comprehensive Cancer Center and The James Cancer Hospital and Solove Research Institute, The Ohio State University, Columbus, OH.
  • Ruppert AS; Comprehensive Cancer Center and The James Cancer Hospital and Solove Research Institute, The Ohio State University, Columbus, OH.
  • Baiocchi RA; Division of Hematology, The Ohio State University, Columbus, OH.
  • Porcu P; Division of Hematology, The Ohio State University, Columbus, OH.
Int J Cancer ; 140(8): 1899-1906, 2017 04 15.
Article em En | MEDLINE | ID: mdl-27943278
Epstein-Barr virus (EBV)-encoded RNAs (EBER) in tumor tissue and cell-free plasma EBV-DNA (pEBVd) are detected in EBV-associated lymphomas. Studies have suggested that EBER+ peripheral T-cell lymphomas (PTCL) have worse prognosis but the role of EBV in these neoplasms remains unclear. pEBVd is quantitative and more easily amenable to standardization than EBER, but frequency of pEBVd detection, clinical impact and agreement with EBER status in PTCL are unknown. We retrospectively assessed frequency of detectable pre-treatment pEBVd, presence of EBER in tumor tissue, and outcomes in 61 of 135 EBV-assessable PTCL patients. Fifteen of 61 patients (24.5%, 95% CI: 14-37%) were pre-treatment pEBVd+, with no significant differences in baseline characteristics or treatment between pEBVd+ and pEBVd- patients. EBER-ISH was performed on 10 pEBVd+ and 35 pEBVd- tumors. All 10 pEBVd+ patients were EBER+, but 9 pEBVd- patients were also EBER+. With median follow up of 24 months (range 1-96), overall survival (OS) was shorter in pEBVd+ compared to pEBVd- patients (13 vs. 72 months; p = 0.04). In our retrospective study, pre-treatment pEBVd was elevated in 25% of PTCL patients, was highly specific for EBER+ tumors, and was associated with shorter survival. pEBVd should be further explored as a prognostic variable and tumor biomarker in PTCL.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prognóstico / DNA Viral / Linfoma de Células T Periférico / Herpesvirus Humano 4 Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Cancer Ano de publicação: 2017 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prognóstico / DNA Viral / Linfoma de Células T Periférico / Herpesvirus Humano 4 Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Cancer Ano de publicação: 2017 Tipo de documento: Article País de publicação: Estados Unidos