Rohner Eliane, Schmidlin Kurt, Zwahlen Marcel, Chakraborty Rana, Clifford Gary, Obel Niels, Grabar Sophie, Verbon Annelies, Noguera-Julian Antoni, Collins Intira Jeannie, Rojo Pablo, Brockmeyer Norbert, Campbell Maria, Chêne Geneviève, Prozesky Hans, Eley Brian, Stefan D Cristina, Davidson Alan, Chimbetete Cleophas, Sawry Shobna, Davies Mary-Ann, Kariminia Azar, Vibol Ung, Sohn Annette, Egger Matthias, Bohlius Julia
Clin Infect Dis. 2016 Nov 1;63(9):1245-1253. doi: 10.1093/cid/ciw519. Epub 2016 Aug 30.
The burden of Kaposi sarcoma (KS) in human immunodeficiency virus (HIV)-infected children and adolescents on combination antiretroviral therapy (cART) has not been compared globally.
We analyzed cohort data from the International Epidemiologic Databases to Evaluate AIDS and the Collaboration of Observational HIV Epidemiological Research in Europe. We included HIV-infected children aged <16 years at cART initiation from 1996 onward. We used Cox models to calculate hazard ratios (HRs), adjusted for region and origin, sex, cART start year, age, and HIV/AIDS stage at cART initiation.
We included 24 991 children from eastern Africa, southern Africa, Europe and Asia; 26 developed KS after starting cART. Incidence rates per 100 000 person-years (PYs) were 86 in eastern Africa (95% confidence interval [CI], 55-133), 11 in southern Africa (95% CI, 4-35), and 81 (95% CI, 26-252) in children of sub-Saharan African (SSA) origin in Europe. The KS incidence rates were 0/100 000 PYs in children of non-SSA origin in Europe (95% CI, 0-50) and in Asia (95% CI, 0-27). KS risk was lower in girls than in boys (adjusted HR [aHR], 0.3; 95% CI, .1-.9) and increased with age (10-15 vs 0-4 years; aHR, 3.4; 95% CI, 1.2-10.1) and advanced HIV/AIDS stage (CDC stage C vs A/B; aHR, 2.4; 95% CI, .8-7.3) at cART initiation.
HIV-infected children from SSA but not those from other regions, have a high risk of developing KS after cART initiation. Early cART initiation in these children might reduce KS risk.
在接受联合抗逆转录病毒治疗(cART)的感染人类免疫缺陷病毒(HIV)的儿童和青少年中,卡波西肉瘤(KS)的负担尚未在全球范围内进行比较。
我们分析了来自国际流行病学数据库评估艾滋病(IeDEA)和欧洲观察性HIV流行病学研究协作组(COHERE)的队列数据。我们纳入了1996年起开始接受cART治疗时年龄小于16岁的HIV感染儿童。我们使用Cox模型计算风险比(HR),并对地区和来源、性别、cART开始年份、年龄以及开始cART治疗时的HIV/AIDS分期进行了调整。
我们纳入了来自东非、南非、欧洲和亚洲的24991名儿童;其中26名在开始cART治疗后发生了KS。每100000人年(PYs)的发病率在东非为86例(95%置信区间[CI],55 - 133),在南非为11例(95%CI,4 - 35),在欧洲的撒哈拉以南非洲(SSA)裔儿童中为81例(95%CI,26 - 252)。在欧洲非SSA裔儿童中KS发病率为0/100000 PYs(95%CI,0 - 50),在亚洲为0/100000 PYs(95%CI,0 - 27)。女孩的KS风险低于男孩(调整后HR[aHR],0.3;95%CI,0.1 - 0.9),并且随着年龄增长(10 - 15岁与0 - 4岁相比;aHR,3.4;95%CI,1.2 - 10.1)以及开始cART治疗时HIV/AIDS分期的进展(美国疾病控制与预防中心[CDC]C期与A/B期相比;aHR,2.4;95%CI,0.8 - 7.3)而增加。
来自SSA的HIV感染儿童在开始cART治疗后发生KS的风险较高,而其他地区的儿童则不然。在这些儿童中尽早开始cART治疗可能会降低KS风险。