Suppr超能文献

RTS,S/AS01 疟疾疫苗——经证实安全有效?

RTS,S/AS01 malaria vaccine-proven safe and effective?

机构信息

Department of Global Public Health, Karolinska Institutet, Stockholm, Sweden.

Bandim Health Project, OPEN, Department of Clinical Research, Odense University Hospital/University of Southern Denmark, Odense, Denmark; Danish Institute of Advanced Science, University of Southern Denmark, Odense, Denmark.

出版信息

Lancet Infect Dis. 2023 Aug;23(8):e318-e322. doi: 10.1016/S1473-3099(23)00126-3. Epub 2023 Apr 20.

Abstract

In October, 2021, WHO recommended that the RTS,S malaria vaccine, with its strong safety profile and high impact, be provided to children from age 5 months in regions with moderate to high Plasmodium falciparum malaria transmission. The evidence base included phase 3 trials in seven African countries and an ongoing malaria vaccine implementation programme (MVIP) in three African countries. We highlight problems with the MVIP mortality data, including potential confounding, inappropriate use of severe malaria as a surrogate marker, a statistically non-significant effect, and assessment after 2 years instead of the stipulated 4 years, which could have inflated the benefits and deflated the risks associated with the vaccine. We conclude that the claimed impact of the MVIP on mortality is not based on enough scientific evidence and that the MVIP findings do not rule out the possibility of increased mortality among vaccinated girls compared with vaccinated boys, as observed in the phase 3 studies. The MVIP should adhere fully to the planned analyses and the data should be made available for independent assessment. Roll-out of the vaccine elsewhere should include rigorous evaluation, especially of its safety.

摘要

2021 年 10 月,世卫组织建议在疟疾流行程度为中高度的地区,为 5 个月大的儿童提供具有良好安全性和高影响力的 RTS,S 疟疾疫苗。该证据基础包括在七个非洲国家进行的 3 期试验和在三个非洲国家正在进行的疟疾疫苗实施规划(MVIP)。我们强调了 MVIP 死亡率数据存在的问题,包括潜在的混杂因素、不当使用严重疟疾作为替代标志物、统计学上无显著效果以及在 2 年后而不是规定的 4 年后进行评估,这可能夸大了疫苗相关的益处并低估了风险。我们得出的结论是,MVIP 对死亡率的声称影响并非基于足够的科学证据,而且 MVIP 的发现并不能排除接种疫苗的女孩比接种疫苗的男孩死亡率增加的可能性,正如 3 期研究中观察到的那样。MVIP 应完全遵守计划的分析,并且应提供数据供独立评估。在其他地方推出该疫苗应包括严格的评估,特别是对其安全性的评估。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验