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High pretreatment plasma Epstein‐Barr virus (EBV) DNA level is a poor prognostic marker in HIV‐associated EBV‐negative diffuse large B‐cell lymphoma in Malawi

机译:在马拉维与艾滋病相关的EBV阴性的弥漫性大B细胞淋巴瘤的治疗前血浆爱泼斯坦-巴尔病毒(EBV)DNA水平高是不良的预后指标

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摘要

Plasma Epstein‐Barr virus (EBV) DNA measurement has established prognostic utility in EBV‐driven lymphomas, where it serves as a circulating tumor DNA marker. The value of plasma EBV measurement may be amplified in sub‐Saharan Africa (SSA), where advanced imaging and molecular technologies for risk stratification are not typically available. However, its utility in diffuse large B‐cell lymphoma (DLBCL) is less certain, given that only a subset of DLBCLs are EBV‐positive. To explore this possibility, we measured plasma EBV DNA at diagnosis in a cohort of patients with DLBCL in Malawi. High plasma EBV DNA at diagnosis (≥3.0 log copies/mL) was associated with decreased overall survival (OS) (  = .048). When stratified by HIV status, the prognostic utility of baseline plasma EBV DNA level was restricted to HIV‐positive patients. Unexpectedly, most HIV‐positive patients with high plasma EBV DNA at diagnosis had EBV‐negative lymphomas, as confirmed by multiple methods. Even in these HIV‐positive patients with EBV‐negative DLBCL, high plasma EBV DNA remained associated with shorter OS (  = .014). These results suggest that EBV reactivation in nontumor cells is a poor prognostic finding even in HIV‐positive patients with convincingly EBV‐negative DLBCL, extending the potential utility of EBV measurement as a valuable and implementable prognostic marker in SSA.
机译:血浆爱泼斯坦-巴尔病毒(EBV)DNA测量已在EBV驱动的淋巴瘤中建立了预后效用,在此可作为循环中的肿瘤DNA标记物。在非洲撒哈拉以南地区(SSA),血浆EBV测量的价值可能会扩大,那里通常没有用于风险分层的先进成像和分子技术。但是,由于仅一部分DLBCL是EBV阳性,因此它在弥漫性大B细胞淋巴瘤(DLBCL)中的效用尚不确定。为了探索这种可能性,我们在马拉维的一组DLBCL患者诊断时测量了血浆EBV DNA。诊断时血浆EBV DNA高(≥3.0log拷贝/ mL)与总体生存率(OS)降低相关(= .048)。当按HIV状况分层时,基线血浆EBV DNA水平的预后效用仅限于HIV阳性患者。出乎意料的是,经多种方法证实,大多数诊断为具有高血浆EBV DNA的HIV阳性患者都患有EBV阴性淋巴瘤。即使在这些HIV阳性,EBV阴性的DLBCL患者中,血浆EBV高的DNA仍然与较短的OS有关(= .014)。这些结果表明,即使在具有令人信服的EBV阴性DLBCL的HIV阳性患者中,非肿瘤细胞中EBV的激活也是一个不良的预后发现,扩展了EBV测量作为SSA中有价值且可实施的预后标志物的潜在用途。

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