Hosek Sybil G, Landovitz Raphael J, Kapogiannis Bill, Siberry George K, Rudy Bret, Rutledge Brandy, Liu Nancy, Harris D Robert, Mulligan Kathleen, Zimet Gregory, Mayer Kenneth H, Anderson Peter, Kiser Jennifer J, Lally Michelle, Brothers Jennifer, Bojan Kelly, Rooney Jim, Wilson Craig M
Stroger Hospital of Cook County, Chicago, Illinois.
University of California-Los Angeles, Los Angeles.
JAMA Pediatr. 2017 Nov 1;171(11):1063-1071. doi: 10.1001/jamapediatrics.2017.2007.
Adolescents represent a key population for implementing preexposure prophylaxis (PrEP) interventions worldwide, yet tenofovir disoproxil fumarate/emtricitabine (TDF/FTC) for PrEP is only licensed for adults.
To examine the safety of and adherence to PrEP along with changes in sexual risk behavior among adolescent men who have sex with men (MSM).
DESIGN, SETTING, AND PARTICIPANTS: Adolescent Medicine Trials Network for HIV/AIDS Interventions 113 (Project PrEPare) was a PrEP demonstration project that evaluated the safety, tolerability, and acceptability of TDF/FTC and patterns of use, rates of adherence, and patterns of sexual risk behavior among healthy young MSM aged 15 to 17 years. Participants were recruited from adolescent medicine clinics and their community partners in 6 US cities, had negative test results for human immunodeficiency virus (HIV) but were at high risk for acquiring an infection, and were willing to participate in a behavioral intervention and accept TDF/FTC as PrEP.
All participants completed an individualized evidence-based behavioral intervention and were provided with daily TDF/FTC as PrEP for 48 weeks.
The main objectives were to: (1) provide additional safety data regarding TDF/FTC use among young MSM who had negative test results for HIV; (2) examine the acceptability, patterns of use, rates of adherence, and measured levels of tenofovir diphosphate in dried blood spots; and (3) examine patterns of risk behavior when young MSM were provided with a behavioral intervention in conjunction with open-label TDF/FTC.
Among 2864 individuals screened (from August 2013 to September 2014), 260 were eligible and 78 were enrolled (mean [SD] age, 16.5 [0.73] years), of whom 2 (3%) were Asian/Pacific Islander, 23 (29%) were black/African American, 11 (14%) were white, 16 (21%) were white Hispanic, and 26 (33%) were other/mixed race/ethnicity. Over 48 weeks of PrEP use, 23 sexually transmitted infections were diagnosed in 12 participants. The HIV seroconversion rate was 6.4 (95% CI: 1.3-18.7) per 100 person-years. Tenofovir diphosphate levels consistent with a high degree of anti-HIV protection (>700 fmol/punch) were found in 42 (54%), 37 (47%), 38 (49%), 22 (28%), 13 (17%), and 17 (22%) participants at weeks 4, 8, 12, 24, 36, and 48, respectively.
Adolescent Medicine Trials Network for HIV/AIDS Interventions 113 enrolled a diverse sample of adolescent MSM at risk for HIV who consented to study participation. Approximately half achieved protective drug levels during the monthly visits, but adherence decreased with quarterly visits. Youth may need additional contact with clinical staff members to maintain high adherence.
clinicaltrials.gov Identifier: NCT01769456.
在全球范围内,青少年是实施暴露前预防(PrEP)干预措施的关键人群,但用于PrEP的富马酸替诺福韦二吡呋酯/恩曲他滨(TDF/FTC)仅被批准用于成年人。
研究男男性行为者(MSM)青少年中PrEP的安全性、依从性以及性风险行为的变化。
设计、地点和参与者:青少年医学艾滋病干预试验网络113(PrEPare项目)是一项PrEP示范项目,评估了TDF/FTC在15至17岁健康年轻MSM中的安全性、耐受性和可接受性,以及使用模式、依从率和性风险行为模式。参与者从美国6个城市的青少年医学诊所及其社区合作伙伴中招募,人类免疫缺陷病毒(HIV)检测结果为阴性,但有感染HIV的高风险,且愿意参与行为干预并接受TDF/FTC作为PrEP。
所有参与者均完成了个体化的循证行为干预,并被提供每日TDF/FTC作为PrEP,为期48周。
主要目标是:(1)提供关于HIV检测结果为阴性的年轻MSM使用TDF/FTC的额外安全性数据;(2)研究可接受性、使用模式、依从率以及干血斑中替诺福韦二磷酸的测量水平;(3)研究在为年轻MSM提供行为干预并联合开放标签TDF/FTC时的风险行为模式。
在2864名被筛查者(2013年8月至2014年9月)中,260人符合条件,78人被纳入研究(平均[标准差]年龄为16.5[0.73]岁),其中2人(3%)为亚裔/太平洋岛民,23人(29%)为黑人/非裔美国人,11人(14%)为白人,16人(21%)为西班牙裔白人,26人(33%)为其他/混合种族/族裔。在48周的PrEP使用期间,12名参与者被诊断出23例性传播感染。HIV血清转化率为每100人年6.4(95%CI:1.3 - 18.7)。在第4、8、12、24、36和48周时,分别有42(54%)、37(47%)、38(49%)、22(28%)、13(17%)和17(22%)名参与者的替诺福韦二磷酸水平与高度抗HIV保护(>700 fmol/打孔)一致。
青少年医学艾滋病干预试验网络113纳入了有HIV感染风险且同意参与研究的多样化MSM青少年样本。在每月随访期间,约一半参与者达到了保护性药物水平,但随着季度随访,依从性下降。青少年可能需要与临床工作人员增加接触以维持高依从性。
clinicaltrials.gov标识符:NCT01769456。