Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Am J Hematol. 2022 Jul;97(7):951-965. doi: 10.1002/ajh.26579. Epub 2022 May 3.
Epstein Barr virus-positive (EBV+) diffuse large B-cell lymphoma (DLBCL), not otherwise specified (NOS) is an entity included in the WHO classification of lymphoid neoplasms since 2016. EBV+ DLBCL, NOS, is an aggressive B-cell lymphoma associated with EBV infection, and a poor prognosis with standard chemotherapeutic approaches.
The diagnosis is made through a careful pathological evaluation. Detection of EBV-encoded RNA (EBER) is considered standard for diagnosis; however, a clear cutoff for percentage of positive cells has not been defined. The differential diagnosis includes plasmablastic lymphoma (PBL), DLBCL associated with chronic inflammation, primary effusion lymphoma (PEL), among others.
RISK-STRATIFICATION: The International Prognostic Index (IPI) and the Oyama score can be used for risk-stratification. The Oyama score includes age >70 years and presence of B symptoms. The expression of CD30 and PD-1/PD-L1 are emerging as potential adverse but targetable biomarkers.
Patients with EBV+ DLBCL, NOS, should be staged and managed following similar guidelines than patients with EBV-negative DLBCL. EBV+ DLBCL, NOS, however, might have a worse prognosis than EBV-negative DLBCL in the era of chemoimmunotherapy. Therefore, the inclusion of patients in clinical trials when available is recommended. There is an opportunity to study and develop targeted therapy in the management of patients with EBV+ DLBCL, NOS.
EBV 阳性(EBV+)弥漫性大 B 细胞淋巴瘤(DLBCL),非特指型(NOS)是 2016 年以来 WHO 淋巴肿瘤分类中的一个实体。EBV+ DLBCL,NOS,是一种与 EBV 感染相关的侵袭性 B 细胞淋巴瘤,采用标准化疗方法预后较差。
通过仔细的病理评估做出诊断。检测 EBV 编码的 RNA(EBER)被认为是诊断的标准;然而,尚未定义阳性细胞百分比的明确截止值。鉴别诊断包括浆母细胞淋巴瘤(PBL)、与慢性炎症相关的 DLBCL、原发性渗出性淋巴瘤(PEL)等。
国际预后指数(IPI)和 Oyama 评分可用于风险分层。Oyama 评分包括年龄>70 岁和存在 B 症状。CD30 和 PD-1/PD-L1 的表达是新兴的潜在不良但可靶向的生物标志物。
EBV+ DLBCL,NOS 的患者应按照与 EBV 阴性 DLBCL 相似的指南进行分期和管理。然而,在化疗免疫治疗时代,EBV+ DLBCL,NOS 比 EBV 阴性 DLBCL 的预后更差。因此,建议在有临床试验时将患者纳入其中。在 EBV+ DLBCL,NOS 的管理中,有机会研究和开发靶向治疗。