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免疫缺陷作为接受联合抗逆转录病毒治疗的 HIV-1 感染患者中非艾滋病定义性恶性肿瘤的风险因素。

Immunodeficiency as a risk factor for non-AIDS-defining malignancies in HIV-1-infected patients receiving combination antiretroviral therapy.

机构信息

HIV Monitoring Foundation, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Clin Infect Dis. 2011 Jun 15;52(12):1458-65. doi: 10.1093/cid/cir207.

Abstract

BACKGROUND

The aim of this study was to investigate the association between immunodeficiency, viremia, and non-AIDS-defining malignancies (NADM).

METHODS

Patients starting combination antiretroviral therapy (cART) as of 1 January 1996 were selected from the AIDS Therapy Evaluation in the Netherlands (ATHENA) cohort. In Cox models, risk factors for NADM were investigated. These included age, sex, transmission route, smoking, alcohol abuse, prior AIDS diagnosis, duration of exposure to cART, and estimated duration of human immunodeficiency virus infection. CD4+ cell count and viral load (VL) were considered as time-updated variables and as measures of cumulative exposure to CD4+ cell counts of < 200, < 350, or < 500 cells/mm³ and detectable VL >50, >400, and >1000 copies/mL, respectively.

RESULTS

In a cohort of 11,459 patients, 236 NADMs were diagnosed; 102 were caused by infection, and 134 were attributable to other causes. Median CD4+ cell count at NADM diagnosis was 340 cells/mm³ (range, 210-540 cells/mm³). Median time to first NADM after starting cART was 5.0 years (range, 2.2-8.2 years). In multivariate models, cumulative exposure to CD4+ cell counts < 200 cells/mm³ remained significant (hazard ratio [HR], 1.12; range, 1.03-1.22) for each additional year of exposure. In stratified analyses, cumulative exposure to CD4+ cell counts < 200 cells/mm³ was associated with malignancies possibly caused by infection (HR, 1.16; range, 1.03-1.31]) but was not associated with other types of cancers. No significant effect of viremia was seen in either type of cancer.

CONCLUSIONS

Cumulative exposure to CD4+ cell counts < 200 cells/mm³ during cART was associated with an increased risk of infection-related non-AIDS-defining malignancies.

摘要

背景

本研究旨在探讨免疫缺陷、病毒血症与非艾滋病定义性恶性肿瘤(NADM)之间的关联。

方法

本研究从 AIDS Therapy Evaluation in the Netherlands(ATHENA)队列中选取了自 1996 年 1 月 1 日起开始联合抗逆转录病毒治疗(cART)的患者。采用 Cox 模型分析 NADM 的危险因素,包括年龄、性别、传播途径、吸烟、酗酒、既往 AIDS 诊断、cART 暴露时间以及人类免疫缺陷病毒感染的估计持续时间。CD4+细胞计数和病毒载量(VL)被视为时间更新变量,并分别作为 CD4+细胞计数<200、<350 和<500 个细胞/mm³以及可检测到的 VL>50、>400 和>1000 拷贝/ml 的累积暴露的衡量指标。

结果

在一个由 11459 名患者组成的队列中,诊断出 236 例 NADM,其中 102 例由感染引起,134 例归因于其他原因。NADM 诊断时的中位 CD4+细胞计数为 340 个细胞/mm³(范围 210-540 个细胞/mm³)。cART 开始后首次发生 NADM 的中位时间为 5.0 年(范围 2.2-8.2 年)。在多变量模型中,CD4+细胞计数<200 个细胞/mm³的累积暴露与每增加一年暴露的风险比(HR)为 1.12(范围 1.03-1.22)仍有显著意义。分层分析显示,CD4+细胞计数<200 个细胞/mm³的累积暴露与可能由感染引起的恶性肿瘤有关(HR,1.16;范围,1.03-1.31),但与其他类型的癌症无关。在任何一种癌症中,病毒血症均无显著影响。

结论

cART 期间 CD4+细胞计数<200 个细胞/mm³的累积暴露与感染相关的非艾滋病定义性恶性肿瘤风险增加有关。

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