Journal
LANCET
Volume 387, Issue 10016, Pages 367-375Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/S0140-6736(15)00725-4
Keywords
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Categories
Funding
- PATH Malaria Vaccine Initiative
- Bill & Melinda Gates Foundation
- Global Good Fund
- Medical Research Council
- UK Department for International Development
- GAVI, the Vaccine Alliance
- WHO
- Global Good Fund of Bellevue, WA, USA
- Medical Research Council (MRC)
- UK Department for International Development (DFID) under the MRC/DFID
- Medical Research Council [G1002284, MR/K010174/1, MR/K010174/1B] Funding Source: researchfish
- MRC [G1002284, MR/K010174/1] Funding Source: UKRI
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Background The phase 3 trial of the RTS, S/AS01 malaria vaccine candidate showed modest efficacy of the vaccine against Plasmodium falciparum malaria, but was not powered to assess mortality endpoints. Impact projections and cost-effectiveness estimates for longer timeframes than the trial follow-up and across a range of settings are needed to inform policy recommendations. We aimed to assess the public health impact and cost-effectiveness of routine use of the RTS, S/AS01 vaccine in African settings. Methods We compared four malaria transmission models and their predictions to assess vaccine cost-effectiveness and impact. We used trial data for follow-up of 32 months or longer to parameterise vaccine protection in the group aged 5-17 months. Estimates of cases, deaths, and disability-adjusted life-years (DALYs) averted were calculated over a 15 year time horizon for a range of levels of Plasmodium falciparum parasite prevalence in 2-10 year olds (PfPR(2-10); range 3-65%). We considered two vaccine schedules: three doses at ages 6, 7.5, and 9 months (three-dose schedule, 90% coverage) and including a fourth dose at age 27 months (four-dose schedule, 72% coverage). We estimated cost-effectiveness in the presence of existing malaria interventions for vaccine prices of US$2-10 per dose. Findings In regions with a PfPR(2-10) of 10-65%, RTS, S/AS01 is predicted to avert a median of 93 940 (range 20490-126540) clinical cases and 394 (127-708) deaths for the three-dose schedule, or 116 480 (31450-160410) clinical cases and 484 (189-859) deaths for the four-dose schedule, per 100 000 fully vaccinated children. A positive impact is also predicted at a PfPR(2-10) of 5-10%, but there is little impact at a prevalence of lower than 3%. At $5 per dose and a PfPR(2-10) of 10-65%, we estimated a median incremental cost-effectiveness ratio compared with current interventions of $30 (range 18-211) per clinical case averted and $80 (44-279) per DALY averted for the three-dose schedule, and of $25 (16-222) and $87 (48-244), respectively, for the four-dose schedule. Higher ICERs were estimated at low PfPR(2-10) levels. Interpretation We predict a significant public health impact and high cost-effectiveness of the RTS, S/AS01 vaccine across a wide range of settings. Decisions about implementation will need to consider levels of malaria burden, the cost-effectiveness and coverage of other malaria interventions, health priorities, financing, and the capacity of the health system to deliver the vaccine.
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