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Adverse events of active and placebo groups in SARS-CoV-2 vaccine randomized trials: A systematic review

BACKGROUND: For safety assessment in clinical trials, adverse events (AEs) are reported for the drug under evaluation and compared with AEs in the placebo group. Little is known about the nature of the AEs associated with clinical trials of SARS-CoV-2 vaccines and the extent to which these can be tr...

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Autores principales: Amanzio, Martina, Mitsikostas, Dimos D, Giovannelli, Fabio, Bartoli, Massimo, Cipriani, Giuseppina Elena, Brown, Walter A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553263/
https://www.ncbi.nlm.nih.gov/pubmed/34729549
http://dx.doi.org/10.1016/j.lanepe.2021.100253
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author Amanzio, Martina
Mitsikostas, Dimos D
Giovannelli, Fabio
Bartoli, Massimo
Cipriani, Giuseppina Elena
Brown, Walter A
author_facet Amanzio, Martina
Mitsikostas, Dimos D
Giovannelli, Fabio
Bartoli, Massimo
Cipriani, Giuseppina Elena
Brown, Walter A
author_sort Amanzio, Martina
collection PubMed
description BACKGROUND: For safety assessment in clinical trials, adverse events (AEs) are reported for the drug under evaluation and compared with AEs in the placebo group. Little is known about the nature of the AEs associated with clinical trials of SARS-CoV-2 vaccines and the extent to which these can be traced to nocebo effects, where negative treatment-related expectations favor their occurrence. METHODS: In our systematic review, we compared the rates of solicited AEs in the active and placebo groups of SARS-CoV-2 vaccines approved by the Western pharmaceutical regulatory agencies. We implemented a search strategy to identify trial-III studies of SARS-CoV-2 vaccines through the PubMed database. We adopted the PRISMA Statement to perform the study selection and the data collection and identified three trial: two mRNA-based (38403 participants) and one adenovirus type (6736 participants). FINDINGS: Relative risks showed that the occurrence of AEs reported in the vaccine groups was higher compared with the placebo groups. The most frequently AEs in both groups were fatigue, headache, local pain, as injection site reactions, and myalgia. In particular, for first doses in placebo recipients, fatigue was reported in 29% and 27% in BNT162b2 and mRNA-1273 groups, respectively, and in 21% of Ad26.COV2.S participants. Headache was reported in 27% in both mRNA groups and in 24% of Ad26.COV2.S recipients. Myalgia was reported in 10% and 14% in mRNA groups (BNT162b2 and mRNA-1273, respectively) and in 13% of Ad26.COV2.S participants. Local pain was reported in 12% and 17% in mRNA groups (BNT162b2 and mRNA-1273, respectively), and in 17% of Ad26.COV2.S recipients. These AEs are more common in the younger population and in the first dose of placebo recipients of the mRNA vaccines. INTERPRETATION: Our results are in agreement with the expectancy theory of nocebo effects and suggest that the AEs associated with COVID-19 vaccines may be related to the nocebo effect. FUNDING: Fondazione CRT - Cassa di Risparmio di Torino, IT (grant number 66346, “GAIA-MENTE” 2019).
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spelling pubmed-85532632021-10-29 Adverse events of active and placebo groups in SARS-CoV-2 vaccine randomized trials: A systematic review Amanzio, Martina Mitsikostas, Dimos D Giovannelli, Fabio Bartoli, Massimo Cipriani, Giuseppina Elena Brown, Walter A Lancet Reg Health Eur Research Paper BACKGROUND: For safety assessment in clinical trials, adverse events (AEs) are reported for the drug under evaluation and compared with AEs in the placebo group. Little is known about the nature of the AEs associated with clinical trials of SARS-CoV-2 vaccines and the extent to which these can be traced to nocebo effects, where negative treatment-related expectations favor their occurrence. METHODS: In our systematic review, we compared the rates of solicited AEs in the active and placebo groups of SARS-CoV-2 vaccines approved by the Western pharmaceutical regulatory agencies. We implemented a search strategy to identify trial-III studies of SARS-CoV-2 vaccines through the PubMed database. We adopted the PRISMA Statement to perform the study selection and the data collection and identified three trial: two mRNA-based (38403 participants) and one adenovirus type (6736 participants). FINDINGS: Relative risks showed that the occurrence of AEs reported in the vaccine groups was higher compared with the placebo groups. The most frequently AEs in both groups were fatigue, headache, local pain, as injection site reactions, and myalgia. In particular, for first doses in placebo recipients, fatigue was reported in 29% and 27% in BNT162b2 and mRNA-1273 groups, respectively, and in 21% of Ad26.COV2.S participants. Headache was reported in 27% in both mRNA groups and in 24% of Ad26.COV2.S recipients. Myalgia was reported in 10% and 14% in mRNA groups (BNT162b2 and mRNA-1273, respectively) and in 13% of Ad26.COV2.S participants. Local pain was reported in 12% and 17% in mRNA groups (BNT162b2 and mRNA-1273, respectively), and in 17% of Ad26.COV2.S recipients. These AEs are more common in the younger population and in the first dose of placebo recipients of the mRNA vaccines. INTERPRETATION: Our results are in agreement with the expectancy theory of nocebo effects and suggest that the AEs associated with COVID-19 vaccines may be related to the nocebo effect. FUNDING: Fondazione CRT - Cassa di Risparmio di Torino, IT (grant number 66346, “GAIA-MENTE” 2019). Elsevier 2021-10-28 /pmc/articles/PMC8553263/ /pubmed/34729549 http://dx.doi.org/10.1016/j.lanepe.2021.100253 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Paper
Amanzio, Martina
Mitsikostas, Dimos D
Giovannelli, Fabio
Bartoli, Massimo
Cipriani, Giuseppina Elena
Brown, Walter A
Adverse events of active and placebo groups in SARS-CoV-2 vaccine randomized trials: A systematic review
title Adverse events of active and placebo groups in SARS-CoV-2 vaccine randomized trials: A systematic review
title_full Adverse events of active and placebo groups in SARS-CoV-2 vaccine randomized trials: A systematic review
title_fullStr Adverse events of active and placebo groups in SARS-CoV-2 vaccine randomized trials: A systematic review
title_full_unstemmed Adverse events of active and placebo groups in SARS-CoV-2 vaccine randomized trials: A systematic review
title_short Adverse events of active and placebo groups in SARS-CoV-2 vaccine randomized trials: A systematic review
title_sort adverse events of active and placebo groups in sars-cov-2 vaccine randomized trials: a systematic review
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553263/
https://www.ncbi.nlm.nih.gov/pubmed/34729549
http://dx.doi.org/10.1016/j.lanepe.2021.100253
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