Microbiology-Immunology and Virology Unit, Centro di Riferimento Oncologico, IRCCS, via F. Gallini 2, 33081 Aviano, Italy.
J Clin Virol. 2012 Apr;53(4):297-301. doi: 10.1016/j.jcv.2011.12.021. Epub 2012 Jan 11.
Despite the era of highly active antiretroviral therapy, non-Hodgkin lymphoma (NHL) remains one of the main causes of death in HIV-infected patients, with a wide variation on the outcome.
We investigated immunological status and EBV, HHV8, HIV viral load in a group of HIV-infected patients at diagnosis of NHL to evaluate their prognostic significance.
Eighty-one consecutive HIV+ NHL patients were studied. CD4 and CD8 cell counts, HHV8 DNA, EBV DNA, HIV RNA and HIV DNA were assessed at diagnosis and at 3 months after chemotherapy initiation. Hazard ratios (HRs) and corresponding 95% confidence intervals (CIs) of disease free survival (DFS) and overall survival (OS) were computed according to CD4 and CD8 cell counts, EBV DNA, HIV RNA and HIV DNA. HRs were, thereafter, computed also for continuous variation of CD4, CD8 cell counts and EBV DNA.
In the multivariate analysis, CD4<160 and CD8<590 cell/μl and EBV DNA≥300 c/ml were independently associated to DFS (HR=2.98; 95%CI: 1.26-7.03; HR=2.65, 95%CI: 1.13-6.19; HR=4.01; 95%CI: 1.81-8.91) and OS (HR=3.32; 95%CI: 1.41-7.83; HR=4.62, 95%CI: 1.91-11.19; HR=3.11, 95%CI: 1.42-6.80). HRs for DFS and OS decreased continuously with increasing CD4 and CD8 cell counts, while they increased continuously with increasing EBV DNA levels.
The association with survival of low CD4 and CD8 cell counts and detectable EBV viremia, measured at lymphoma's diagnosis, identified three independent prognostic biomarkers that might help in the management of NHL HIV+ patients, offering complementary information in the ascertainment of their outcome.
尽管采用了高效抗逆转录病毒疗法,非霍奇金淋巴瘤(NHL)仍是 HIV 感染者的主要死亡原因之一,其预后存在广泛差异。
我们研究了一组 HIV 感染 NHL 患者在诊断时的免疫状态和 EBV、HHV8、HIV 病毒载量,以评估其预后意义。
研究了 81 例连续的 HIV+ NHL 患者。在诊断时和化疗开始后 3 个月评估 CD4 和 CD8 细胞计数、HHV8 DNA、EBV DNA、HIV RNA 和 HIV DNA。根据 CD4 和 CD8 细胞计数、EBV DNA、HIV RNA 和 HIV DNA 计算无病生存(DFS)和总生存(OS)的危险比(HR)和相应的 95%置信区间(CI)。此后,还根据 CD4、CD8 细胞计数和 EBV DNA 的连续变化计算了 HR。
在多变量分析中,CD4<160 和 CD8<590 细胞/μl 和 EBV DNA≥300 c/ml 与 DFS(HR=2.98;95%CI:1.26-7.03;HR=2.65,95%CI:1.13-6.19;HR=4.01;95%CI:1.81-8.91)和 OS(HR=3.32;95%CI:1.41-7.83;HR=4.62,95%CI:1.91-11.19;HR=3.11,95%CI:1.42-6.80)独立相关。随着 CD4 和 CD8 细胞计数的增加,DFS 和 OS 的 HR 逐渐降低,而随着 EBV DNA 水平的增加,HR 逐渐增加。
在 NHL HIV+患者的管理中,在淋巴瘤诊断时测量的低 CD4 和 CD8 细胞计数和可检测的 EBV 病毒血症与生存相关,确定了三个独立的预后生物标志物,可为评估其预后提供补充信息。