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Feasibility, safety, and impact of the RTS,S/AS01E malaria vaccine when implemented through national immunisation programmes: evaluation of cluster-randomised introduction of the vaccine in Ghana, Kenya, and Malawi.
Asante, Kwaku Poku; Mathanga, Don P; Milligan, Paul; Akech, Samuel; Oduro, Abraham; Mwapasa, Victor; Moore, Kerryn A; Kwambai, Titus K; Hamel, Mary J; Gyan, Thomas; Westercamp, Nelli; Kapito-Tembo, Atupele; Njuguna, Patricia; Ansong, Daniel; Kariuki, Simon; Mvalo, Tisungane; Snell, Paul; Schellenberg, David; Welega, Paul; Otieno, Lucas; Chimala, Alfred; Afari, Edwin A; Bejon, Philip; Maleta, Kenneth; Agbenyega, Tsiri; Snow, Robert W; Zulu, Madaliso; Chinkhumba, Jobiba; Samuels, Aaron M.
Affiliation
  • Asante KP; Kintampo Health Research Centre, Research and Development Division, Ghana Health Service, Kintampo North Municipality, Ghana; London School of Hygiene & Tropical Medicine, London, UK. Electronic address: kwakupoku.asante@kintampo-hrc.org.
  • Mathanga DP; School of Public Health, Kamuzu University of Health Sciences, Blantyre, Malawi; Malaria Alert Centre, Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Milligan P; London School of Hygiene & Tropical Medicine, London, UK. Electronic address: paul.milligan@lshtm.ac.uk.
  • Akech S; Kenya Medical Research Institute (KEMRI)-Wellcome Trust Research Programme, Nairobi, Kenya.
  • Oduro A; Navrongo Health Research Centre, Research and Development Division, Ghana Health Service, Accra, Ghana.
  • Mwapasa V; School of Public Health, Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Moore KA; London School of Hygiene & Tropical Medicine, London, UK; Murdoch Children's Research Institute, Infection and Immunity, New Vaccines, Parkville, VIC, Australia.
  • Kwambai TK; Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Kisumu, Kenya.
  • Hamel MJ; Department of Immunizations, Vaccines, and Biologicals, WHO, Geneva, Switzerland.
  • Gyan T; Kintampo Health Research Centre, Research and Development Division, Ghana Health Service, Kintampo North Municipality, Ghana.
  • Westercamp N; Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Kapito-Tembo A; School of Public Health, Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Njuguna P; Global Malaria Programme, WHO, Geneva, Switzerland.
  • Ansong D; Agogo Malaria Research Centre, Agogo, Ghana; Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
  • Kariuki S; Centre for Global Health Research, KEMRI, Kisumu, Kenya.
  • Mvalo T; University of North Carolina Project-Malawi, Lilongwe, Malawi.
  • Snell P; London School of Hygiene & Tropical Medicine, London, UK.
  • Schellenberg D; Global Malaria Programme, WHO, Geneva, Switzerland.
  • Welega P; Navrongo Health Research Centre, Research and Development Division, Ghana Health Service, Accra, Ghana.
  • Otieno L; KEMRI-US Army Medical Research Directorate-Africa, Kisumu, Kenya.
  • Chimala A; Malaria Alert Centre, Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Afari EA; School of Public Health, University of Ghana, Accra, Ghana.
  • Bejon P; Kenya Medical Research Institute (KEMRI)-Wellcome Trust Research Programme, Nairobi, Kenya; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
  • Maleta K; School of Public Health, Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Agbenyega T; Agogo Malaria Research Centre, Agogo, Ghana; Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
  • Snow RW; Kenya Medical Research Institute (KEMRI)-Wellcome Trust Research Programme, Nairobi, Kenya; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
  • Zulu M; University of North Carolina Project-Malawi, Lilongwe, Malawi.
  • Chinkhumba J; School of Public Health, Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Samuels AM; Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Kisumu, Kenya; Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA, USA. Electro
Lancet ; 403(10437): 1660-1670, 2024 Apr 27.
Article in En | MEDLINE | ID: mdl-38583454
ABSTRACT

BACKGROUND:

The RTS,S/AS01E malaria vaccine (RTS,S) was introduced by national immunisation programmes in Ghana, Kenya, and Malawi in 2019 in large-scale pilot schemes. We aimed to address questions about feasibility and impact, and to assess safety signals that had been observed in the phase 3 trial that included an excess of meningitis and cerebral malaria cases in RTS,S recipients, and the possibility of an excess of deaths among girls who received RTS,S than in controls, to inform decisions about wider use.

METHODS:

In this prospective evaluation, 158 geographical clusters (66 districts in Ghana; 46 sub-counties in Kenya; and 46 groups of immunisation clinic catchment areas in Malawi) were randomly assigned to early or delayed introduction of RTS,S, with three doses to be administered between the ages of 5 months and 9 months and a fourth dose at the age of approximately 2 years. Primary outcomes of the evaluation, planned over 4 years, were mortality from all causes except injury (impact), hospital admission with severe malaria (impact), hospital admission with meningitis or cerebral malaria (safety), deaths in girls compared with boys (safety), and vaccination coverage (feasibility). Mortality was monitored in children aged 1-59 months throughout the pilot areas. Surveillance for meningitis and severe malaria was established in eight sentinel hospitals in Ghana, six in Kenya, and four in Malawi. Vaccine uptake was measured in surveys of children aged 12-23 months about 18 months after vaccine introduction. We estimated that sufficient data would have accrued after 24 months to evaluate each of the safety signals and the impact on severe malaria in a pooled analysis of the data from the three countries. We estimated incidence rate ratios (IRRs) by comparing the ratio of the number of events in children age-eligible to have received at least one dose of the vaccine (for safety outcomes), or age-eligible to have received three doses (for impact outcomes), to that in non-eligible age groups in implementation areas with the equivalent ratio in comparison areas. To establish whether there was evidence of a difference between girls and boys in the vaccine's impact on mortality, the female-to-male mortality ratio in age groups eligible to receive the vaccine (relative to the ratio in non-eligible children) was compared between implementation and comparison areas. Preliminary findings contributed to WHO's recommendation in 2021 for widespread use of RTS,S in areas of moderate-to-high malaria transmission.

FINDINGS:

By April 30, 2021, 652 673 children had received at least one dose of RTS,S and 494 745 children had received three doses. Coverage of the first dose was 76% in Ghana, 79% in Kenya, and 73% in Malawi, and coverage of the third dose was 66% in Ghana, 62% in Kenya, and 62% in Malawi. 26 285 children aged 1-59 months were admitted to sentinel hospitals and 13 198 deaths were reported through mortality surveillance. Among children eligible to have received at least one dose of RTS,S, there was no evidence of an excess of meningitis or cerebral malaria cases in implementation areas compared with comparison areas (hospital admission with meningitis IRR 0·63 [95% CI 0·22-1·79]; hospital admission with cerebral malaria IRR 1·03 [95% CI 0·61-1·74]). The impact of RTS,S introduction on mortality was similar for girls and boys (relative mortality ratio 1·03 [95% CI 0·88-1·21]). Among children eligible for three vaccine doses, RTS,S introduction was associated with a 32% reduction (95% CI 5-51%) in hospital admission with severe malaria, and a 9% reduction (95% CI 0-18%) in all-cause mortality (excluding injury).

INTERPRETATION:

In the first 2 years of implementation of RTS,S, the three primary doses were effectively deployed through national immunisation programmes. There was no evidence of the safety signals that had been observed in the phase 3 trial, and introduction of the vaccine was associated with substantial reductions in hospital admission with severe malaria. Evaluation continues to assess the impact of four doses of RTS,S.

FUNDING:

Gavi, the Vaccine Alliance; the Global Fund to Fight AIDS, Tuberculosis and Malaria; and Unitaid.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Feasibility Studies / Malaria, Cerebral / Malaria Vaccines / Immunization Programs Limits: Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: Lancet Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Feasibility Studies / Malaria, Cerebral / Malaria Vaccines / Immunization Programs Limits: Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: Lancet Year: 2024 Type: Article