EBV-positive diffuse large B-cell lymphoma, not otherwise specified: 2022 update on diagnosis, risk-stratification, and management

被引:60
作者
Malpica, Luis [1 ]
Marques-Piubelli, Mario L. [2 ]
Beltran, Brady E. [3 ,4 ]
Chavez, Julio C. [5 ]
Miranda, Roberto N. [6 ]
Castillo, Jorge J. [7 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Lymphoma & Myeloma, 1515 Holcombe Blv, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Translat Mol Pathol, Houston, TX 77030 USA
[3] Hosp Nacl Edgardo Rebagliati Martins, Dept Radiotherapy & Oncol, Lima, Peru
[4] Univ Ricardo Palma, Inst Ciencias Biomed, Lima, Peru
[5] H Lee Moffitt Canc Ctr & Res Inst, Dept Malignant Hematol, Tampa, FL USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Hematopathol, Houston, TX 77030 USA
[7] Harvard Med Sch, Div Hematol Malignancies, Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
EPSTEIN-BARR-VIRUS; DEATH-LIGAND; LYMPHOPROLIFERATIVE DISORDERS; T-CELLS; ADOPTIVE TRANSFER; GENE-EXPRESSION; RITUXIMAB-CHOP; BRENTUXIMAB VEDOTIN; PROGNOSTIC IMPACT; BURKITT-LYMPHOMA;
D O I
10.1002/ajh.26579
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Disease Overview 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. Diagnosis 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. Management 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.
引用
收藏
页码:951 / 965
页数:15
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