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RTS,S/AS01疟疾疫苗3期试验在婴儿中的疗效:一项系统评价和荟萃分析。

Efficacy of Phase 3 Trial of RTS, S/AS01 Malaria Vaccine in infants: a systematic review and meta-analysis.

作者信息

Mahmoudi Shima, Keshavarz Hossein

机构信息

a Pediatric Infectious Disease Research Center, Tehran University of Medical Science , Tehran , Iran.

b Center for Research of Endemic Parasites of Iran (CREPI), Tehran University of Medical Sciences , Tehran , Iran.

出版信息

Hum Vaccin Immunother. 2017 Jan 6:0. doi: 10.1080/21645515.2016.1271686.

Abstract

Although vaccines would be the ideal tool for control, prevention, elimination, and eradication of many infectious diseases, developing of parasites vaccines such as malaria vaccine is very complex. The most advanced malaria vaccine candidate is RTS,S, a pre-erythrocytic vaccine for which pivotal phase III trial design is underway. Few recent malaria vaccine review articles have attempted to outline of all clinical trials that have occurred globally and no meta-analysis was performed on efficacy of Phase 3 Trial of RTS, S/AS01 Malaria vaccine up to now in infants. Therefore, a systematic review and meta-analysis was carried out to review new and existing data on efficacy of Phase 3 Trial of RTS, S/AS01 Malaria Vaccine in infants. The electronic databases searched were Pubmed (1965-present) and Web of Science (1970-present) (Search date: May, 2016). After full-text review of the papers evaluating clinical/severe malaria in several well-designed phase III field efficacy trials, 5 were determined to meet the eligibility criteria for inclusion in the systematic review. Four out of the 5 publications dealing with efficacy of Phase 3 Trial of RTS, S/AS01 malaria vaccine were included in the qualitative analysis. Pooled estimate of vaccine efficacy in clinical and severe malaria in children aged 5-17 mo was 29% (95% CL: 19%-46%) and 39% (95% CI 20%-74%), while this estimate vaccine in clinical and severe malaria in children aged 6-12 mo was 19% (95% CI 14%-24%) and 21 (95% CI 19%-37%), respectively. On the other hand, higher VE was seen in both per- protocol and intention-to-treat population in children aged 5-17 than the children aged 6-12 mo. The results of this meta-analysis suggest that this candidate malaria vaccine has relatively little efficacy, and the vaccine apparently will not meet the goal of malaria eradication by itself.

摘要

尽管疫苗是控制、预防、消除和根除许多传染病的理想工具,但开发诸如疟疾疫苗等寄生虫疫苗非常复杂。最先进的疟疾候选疫苗是RTS,S,这是一种针对红细胞前期的疫苗,其关键的III期试验设计正在进行中。最近很少有疟疾疫苗综述文章试图概述全球范围内已开展的所有临床试验,并且截至目前尚未对RTS,S/AS01疟疾疫苗在婴儿中的III期试验疗效进行荟萃分析。因此,开展了一项系统综述和荟萃分析,以回顾RTS,S/AS01疟疾疫苗在婴儿中的III期试验疗效的新数据和现有数据。检索的电子数据库为Pubmed(1965年至今)和Web of Science(1970年至今)(检索日期:2016年5月)。在对多项精心设计的III期现场疗效试验中评估临床/重症疟疾的论文进行全文审查后,确定有5篇符合纳入系统综述的资格标准。5篇关于RTS,S/AS01疟疾疫苗III期试验疗效的出版物中有4篇被纳入定性分析。5至17个月龄儿童临床和重症疟疾的疫苗疗效合并估计值分别为29%(95%CI:19%-46%)和39%(95%CI:20%-74%),而6至12个月龄儿童临床和重症疟疾的该估计值分别为19%(95%CI:14%-24%)和21%(95%CI:19%-37%)。另一方面,5至17岁儿童在符合方案人群和意向性分析人群中的疫苗效力均高于6至12个月龄儿童。该荟萃分析结果表明,这种候选疟疾疫苗的疗效相对较低,而且该疫苗显然无法独自实现根除疟疾的目标。

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