TY - JOUR
T1 - Reappraisal of Epstein–Barr virus (EBV) in diffuse large B-cell lymphoma (DLBCL)
T2 - comparative analysis between EBV-positive and EBV-negative DLBCL with EBV-positive bystander cells
AU - Ohashi, Akiko
AU - Kato, Seiichi
AU - Okamoto, Akinao
AU - Inaguma, Yoko
AU - Satou, Akira
AU - Tsuzuki, Toyonori
AU - Emi, Nobuhiko
AU - Okamoto, Masataka
AU - Nakamura, Shigeo
N1 - Publisher Copyright:
© 2017 John Wiley & Sons Ltd
PY - 2017/7
Y1 - 2017/7
N2 - Aims: Epstein–Barr virus (EBV)-positive diffuse large B-cell lymphoma (DLBCL) not otherwise specified is defined as monoclonal EBV+ B-cell proliferation affecting patients without any known immunosuppression. Non-neoplastic EBV+ cells proliferating in or adjacent to EBV− DLBCL were reported recently, but their clinical significance is unclear. Thus, the aim of this study was to investigate the prognostic impact of EBV+ cells in DLBCL. Methods and results: We compared the clinicopathological characteristics of 30 EBV+ DLBCL patients and 29 and 604 EBV− DLBCL patients with and without EBV+ bystander cells (median age of onset 71, 67 and 62 years, respectively). Both EBV+ DLBCL patients and EBV− DLBCL patients with EBV+ bystander cells tended to have high and high–intermediate International Prognostic Index scores (60% and 59%, respectively), as compared with only 46% of EBV− DLBCL patients without EBV+ bystander cells. EBV− DLBCL patients with EBV+ bystander cells showed a significantly higher incidence of lung involvement than those without EBV+ bystander cells (10% versus 2%, P < 0.05). Furthermore, EBV+ DLBCL patients and EBV− DLBCL patients with EBV+ bystander cells had a poorer prognosis than patients without any detectable EBV+ cells [median overall survival (OS) of 100 months and 40 months versus not reached, P < 0.01]. Notably, EBV+ DLBCL patients and EBV− DLBCL patients with EBV+ bystander cells treated with rituximab showed overlapping survival curves (OS, P = 0.77; progression-free survival, P = 1.0). Conclusions: EBV− DLBCL with bystander EBV+ cells has similar clinical characteristics to EBV+ DLBCL. DLBCL with EBV+ bystander cells may be related to both age-related and microenvironment-related immunological deterioration.
AB - Aims: Epstein–Barr virus (EBV)-positive diffuse large B-cell lymphoma (DLBCL) not otherwise specified is defined as monoclonal EBV+ B-cell proliferation affecting patients without any known immunosuppression. Non-neoplastic EBV+ cells proliferating in or adjacent to EBV− DLBCL were reported recently, but their clinical significance is unclear. Thus, the aim of this study was to investigate the prognostic impact of EBV+ cells in DLBCL. Methods and results: We compared the clinicopathological characteristics of 30 EBV+ DLBCL patients and 29 and 604 EBV− DLBCL patients with and without EBV+ bystander cells (median age of onset 71, 67 and 62 years, respectively). Both EBV+ DLBCL patients and EBV− DLBCL patients with EBV+ bystander cells tended to have high and high–intermediate International Prognostic Index scores (60% and 59%, respectively), as compared with only 46% of EBV− DLBCL patients without EBV+ bystander cells. EBV− DLBCL patients with EBV+ bystander cells showed a significantly higher incidence of lung involvement than those without EBV+ bystander cells (10% versus 2%, P < 0.05). Furthermore, EBV+ DLBCL patients and EBV− DLBCL patients with EBV+ bystander cells had a poorer prognosis than patients without any detectable EBV+ cells [median overall survival (OS) of 100 months and 40 months versus not reached, P < 0.01]. Notably, EBV+ DLBCL patients and EBV− DLBCL patients with EBV+ bystander cells treated with rituximab showed overlapping survival curves (OS, P = 0.77; progression-free survival, P = 1.0). Conclusions: EBV− DLBCL with bystander EBV+ cells has similar clinical characteristics to EBV+ DLBCL. DLBCL with EBV+ bystander cells may be related to both age-related and microenvironment-related immunological deterioration.
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U2 - 10.1111/his.13197
DO - 10.1111/his.13197
M3 - Article
C2 - 28231401
AN - SCOPUS:85017604012
SN - 0309-0167
VL - 71
SP - 89
EP - 97
JO - Histopathology
JF - Histopathology
IS - 1
ER -