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The prognostic significance of EBV DNA load and EBER status in diagnostic specimens from diffuse large B‐cell lymphoma patients
Author(s) -
Okamoto Akinao,
Yanada Masamitsu,
Inaguma Yoko,
Tokuda Masutaka,
Morishima Satoko,
Kanie Tadaharu,
Yamamoto Yukiya,
Mizuta Shuichi,
Akatsuka Yoshiki,
Yoshikawa Tetsushi,
Mizoguchi Yoshikazu,
Nakamura Shigeo,
Okamoto Masataka,
Emi Nobuhiko
Publication year - 2017
Publication title -
hematological oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 44
eISSN - 1099-1069
pISSN - 0278-0232
DOI - 10.1002/hon.2245
Subject(s) - viral load , lymphoma , diffuse large b cell lymphoma , epstein–barr virus , in situ hybridization , virus , medicine , pathology , biology , immunology , gene , genetics , gene expression
Epstein–Barr virus (EBV)‐encoded small RNA in situ hybridization (EBER‐ISH) is a widely accepted method to evaluate EBV involvement in diffuse large B‐cell lymphoma (DLBCL), although little is known regarding associations between EBV DNA load and the EBER status and whether EBV DNA load data provide additional clinical information. In this study, we quantified EBV DNA load in diagnostic specimens from DLBCL patients diagnosed at our hospital to evaluate clinical implications of EBV DNA load in diagnostic specimens as contrasted with EBER‐ISH. Among 140 DLBCL patients without underlying immunodeficiency, 51 were evaluable for both EBER and EBV DNA load, 83 for EBER only and one for EBV DNA load only. The median EBV DNA load was 708 copies/µg. Although EBV DNA load was significantly higher for EBER‐positive patients than for EBER‐negative patients ( p  < 0.001), EBV DNA was detected in up to 72% of EBER‐negative patients. Progression‐free survival and overall survival were significantly worse for patients with EBV DNA load above 700 copies/µg than for those with EBV DNA load below 700 copies/µg ( p  = 0.009 and p  = 0.003); they were also significantly worse for EBER‐positive patients than for EBER‐negative patients ( p  < 0.001 and p  = 0.001). Even among EBER‐negative patients, higher EBV DNA load conferred worse progression‐free survival and overall survival ( p  = 0.041 and p  = 0.013). These findings indicate that EBV DNA load in diagnostic specimens is not a simple surrogate for the EBER status and may be a potential biomarker associated with EBV involvement and prognosis in DLBCL. Copyright © 2015 John Wiley & Sons, Ltd.

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