Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27599, USA.
Clin Infect Dis. 2013 Sep;57(5):756-64. doi: 10.1093/cid/cit369. Epub 2013 Jun 4.
Cancer is an important cause of morbidity and mortality in individuals infected with human immunodeficiency virus (HIV), but patterns of cancer incidence after combination antiretroviral therapy (ART) initiation remain poorly characterized.
We evaluated the incidence and timing of cancer diagnoses among patients initiating ART between 1996 and 2011 in a collaboration of 8 US clinical HIV cohorts. Poisson regression was used to estimate incidence rates. Cox regression was used to identify demographic and clinical characteristics associated with cancer incidence after ART initiation.
At initiation of first combination ART among 11 485 patients, median year was 2004 (interquartile range [IQR], 2000-2007) and median CD4 count was 202 cells/mm(3) (IQR, 61-338). Incidence rates for Kaposi sarcoma (KS) and lymphomas were highest in the first 6 months after ART initiation (P < .001) and plateaued thereafter, while incidence rates for all other cancers combined increased from 416 to 615 cases per 100 000 person-years from 1 to 10 years after ART initiation (average 7% increase per year; 95% confidence interval, 2%-13%). Lower CD4 count at ART initiation was associated with greater risk of KS, lymphoma, and human papillomavirus-related cancer. Calendar year of ART initiation was not associated with cancer incidence.
KS and lymphoma rates were highest immediately following ART initiation, particularly among patients with low CD4 cell counts, whereas other cancers increased with time on ART, likely reflecting increased cancer risk with aging. Our results underscore recommendations for earlier HIV diagnosis followed by prompt ART initiation along with ongoing aggressive cancer screening and prevention efforts throughout the course of HIV care.
癌症是感染人类免疫缺陷病毒(HIV)个体发病和死亡的重要原因,但在开始联合抗逆转录病毒治疗(ART)后癌症发病模式仍未得到很好的描述。
我们评估了 1996 年至 2011 年间 8 个美国临床 HIV 队列合作中开始 ART 的患者癌症诊断的发生率和时间。泊松回归用于估计发病率。Cox 回归用于确定 ART 后癌症发病的人口统计学和临床特征。
在 11485 名患者开始首次联合 ART 时,中位数年份为 2004 年(四分位距[IQR],2000-2007 年),中位数 CD4 计数为 202 个细胞/mm3(IQR,61-338 个细胞/mm3)。ART 开始后 6 个月内 Kaposi 肉瘤(KS)和淋巴瘤的发病率最高(P <.001),此后趋于平稳,而所有其他癌症的合并发病率从 ART 开始后 1 年的 416 例/100000 人年增加到 10 年的 615 例/100000 人年(平均每年增加 7%;95%置信区间,2%-13%)。ART 开始时 CD4 计数较低与 KS、淋巴瘤和人乳头瘤病毒相关癌症的风险增加相关。ART 开始的日历年份与癌症发病率无关。
KS 和淋巴瘤的发病率在 ART 开始后立即达到最高水平,尤其是在 CD4 细胞计数较低的患者中,而其他癌症随着 ART 的时间增加而增加,这可能反映出随着年龄的增长癌症风险增加。我们的研究结果强调了 HIV 早期诊断后立即开始 ART 的建议,以及在整个 HIV 护理过程中持续进行积极的癌症筛查和预防工作。