Still Far to Go With Characterisation of Molecular and Genetic Features of Diffuse Large B-Cell Lymphoma in People Living With HIV: A Scoping Review

被引:1
作者
Manyau, Maudy C. P. [1 ,2 ]
Zambuko, Blessing [3 ]
Chatambudza, Moses [1 ]
Zhou, Danai T. [1 ,2 ]
Manasa, Justen [1 ,2 ]
机构
[1] Univ Zimbabwe, Dept Lab Diagnost & Invest Sci, Harare, Zimbabwe
[2] Biomed Res & Training Inst, Harare, Zimbabwe
[3] Lancet Labs, Pathol, Harare, Zimbabwe
来源
ONCOLOGY REVIEWS | 2024年 / 18卷
基金
美国国家卫生研究院;
关键词
non-Hodgkin lymphoma; HIV/AIDS; molecular pathology histogenesis; CD10; BCL6; cyclin H; MUM1; CD138; HUMAN-IMMUNODEFICIENCY-VIRUS; AIDS-RELATED LYMPHOMAS; ACTIVE ANTIRETROVIRAL THERAPY; EXPRESSION PROFILE; IMMUNE ACTIVATION; OF-ORIGIN; CLASSIFICATION; SURVIVAL; MARKERS; MUTATIONS;
D O I
10.3389/or.2024.1375291
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Diffuse large B-cell lymphoma (DLBCL) accounts for half of non-Hodgkin lymphoma cases in people living with human immunodeficiency syndrome (PLWH). The interplay of viremia, immune dysregulation and co-infection with oncogenic viruses play a role in pathogenesis of DLBCL in PLWH (HIV-DLBCL). This scoping review aimed to describe the molecular landscape of HIV-DLBCL, investigate the impact of biomarker on clinical outcomes and describe technologies used to characterise HIV-DLBCL. Thirty-two papers published between 2001 and 2023 were included in this review. Samples of HIV-DLBCL were relatively small (16-110). Cohort effects influenced frequencies of molecular characteristics hence their impact on survival was not clear. Molecular features were distinct from HIV-unrelated DLBCL. The most frequently assessed characteristic was cell of origin (81.3% of studies). Somatic mutations were the least researched (6.3% of studies). Overall, biomarker identification in HIV-DLBCL requires broader richer data from larger or pooled samples using more powerful techniques such as next-generation sequencing.
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页数:10
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