Evidence map›Paper›PMID 26549466›Full record

ArticleLancet (London, England)2016

Public health impact and cost-effectiveness of the RTS,S/AS01 malaria vaccine: a systematic comparison of predictions from four mathematical models.

Melissa A Penny, Robert Verity, Caitlin A Bever, Christophe Sauboin, Katya Galactionova, Stefan Flasche, Michael T White, Edward A Wenger, Nicolas Van de Velde, Peter Pemberton-Ross and 6 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Lancet (London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03143218 (A Phase IIIB Comparative Trial of Seasonal Vaccination With the Malaria Vaccine RTS,S/AS01, Seasonal Malaria Chemoprevention and of the Two Interventions Combined), which is not on this map. Cited by 126 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed, 4 pooled it
20.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03143218 phase3completednot on this mapstarted 2017, after this paper: background citation

A Phase IIIB Comparative Trial of Seasonal Vaccination With the Malaria Vaccine RTS,S/AS01, Seasonal Malaria Chemoprevention and of the Two Interventions Combined

TypeinterventionalSponsorLondon School of Hygiene and Tropical MedicineRan2017 to 2020Enrolled5,920ConditionsMalaria,Falciparum, Children, OnlyArmsRABIPUR®, RTS,S/AS01, SMC with SP+AQ, SMC placebo
3 · Its place in the literature

Who cites it

126 citing papers in PubMed, 4 syntheses or guidelines pooled it, 244 citations in OpenAlex.

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66 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 9 institutions in 4 countries.

Melissa A PennyDepartment of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Basel, Switzerland; University of Basel, Basel, Switzerland. Electronic address: melissa.penny@unibas.ch.
Robert VerityMedical Research Council Centre for Outbreak Analysis and Modelling, Imperial College London, London, UK.
Caitlin A BeverInstitute for Disease Modeling, Bellevue, WA, USA.
Christophe SauboinGSK Vaccines, Wavre, Belgium.
Katya GalactionovaDepartment of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Basel, Switzerland; University of Basel, Basel, Switzerland.
Stefan FlascheDepartment of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.
Michael T WhiteMedical Research Council Centre for Outbreak Analysis and Modelling, Imperial College London, London, UK.
Edward A WengerInstitute for Disease Modeling, Bellevue, WA, USA.
Nicolas Van de VeldeGSK Vaccines, Wavre, Belgium.
Peter Pemberton-RossDepartment of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Basel, Switzerland; University of Basel, Basel, Switzerland.
Jamie T GriffinMedical Research Council Centre for Outbreak Analysis and Modelling, Imperial College London, London, UK.
Thomas A SmithDepartment of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Basel, Switzerland; University of Basel, Basel, Switzerland.
Philip A EckhoffInstitute for Disease Modeling, Bellevue, WA, USA.
Farzana MuhibPATH, Washington, DC, USA.
Mark JitDepartment of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK; Modelling and Economics Unit, Public Health England, London, UK.
Azra C GhaniMedical Research Council Centre for Outbreak Analysis and Modelling, Imperial College London, London, UK.
Imperial College London · GBSwiss Tropical and Public Health Institute · CHGlaxoSmithKline (Belgium) · BEInstitute for Disease Modeling · USLondon School of Hygiene & Tropical Medicine · GBBellevue Hospital Center · USMedical Research Council · GBProgram for Appropriate Technology in Health · USUniversity of Basel · CH

Funding

Medical Research Council G1002284Medical Research Council MR/K010174/1
6 · The paper itself

Abstract

backgroundThe 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.

methodsWe 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 (PfPR2-10; 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.

findingsIn regions with a PfPR2-10 of 10-65%, RTS,S/AS01 is predicted to avert a median of 93,940 (range 20,490-126,540) clinical cases and 394 (127-708) deaths for the three-dose schedule, or 116,480 (31,450-160,410) 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 PfPR2-10 of 5-10%, but there is little impact at a prevalence of lower than 3%. At $5 per dose and a PfPR2-10 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 PfPR2-10 levels.

interpretationWe 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.

fundingPATH Malaria Vaccine Initiative; Bill & Melinda Gates Foundation; Global Good Fund; Medical Research Council; UK Department for International Development; GAVI, the Vaccine Alliance; WHO.

Indexed as

Models, TheoreticalPublic HealthAfricaClinical Trials, Phase III as TopicCost-Benefit AnalysisHumansImmunization ScheduleInfantMalaria, FalciparumMalaria VaccinesMulticenter Studies as TopicMalaria Vaccines

Identifiers

PMID26549466
PMCPMC4723722
OpenAlexW2158417058

What OpenQuestion holds

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LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.