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Adverse drug reactions to the three doses of the severe acute respiratory syndrome coronavirus 2 (SARS-COV-2) mRNA-1273 vaccine in a cohort of cancer patients under active treatment of a tertiary hospital in Madrid, Spain.

Authors :
Benitez Fuentes JD
de Luna Aguilar A
Jimenez Ortega AF
Flores Navarro P
Bartolomé Arcilla J
Baos Muñoz E
Delgado-Iribarren García-Campero A
Gil Useros S
Martinez Capella I
Llorente Sanz L
Torrego Ellacuría M
Pérez Segura P
Source :
F1000Research [F1000Res] 2022 Apr 19; Vol. 11, pp. 434. Date of Electronic Publication: 2022 Apr 19 (Print Publication: 2022).
Publication Year :
2022

Abstract

Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines efficacy and safety have been tested in phase 3 studies in which cancer patients were not included or were underrepresented. Methods: The objective of this study is to evaluate the safety profile of the mRNA-1273 vaccine across cancer patients and its relationship to patients' demographics. We selected from our records all 18-years or older solid cancer patients under active treatment vaccinated with the complete three-dose schedule mRNA-1273 vaccine whose adverse drug reactions (ADRs)  after each dose were recorded. Medical records were reviewed retrospectively to collect data between April 19, 2021, and December 31, 2021. Patients with documented previous infection by SARS-Cov-2 were excluded. Results: A total of 93 patients met the inclusion criteria. Local ADRs were reported more frequently after the first and second dose than after the third (41.9%, 43% and 31.1% of the patients respectively), while systemic ADRs followed the opposite pattern (16.1%, 34.4% and 52.6% of the patients respectively). We found a statistically significant association between sex and systemic adverse reactions after the third dose, p < 0.001 and between systemic adverse reactions after the second dose and systemic adverse reactions after the third dose, p = 0.001 A significant linear trend, p = 0.012, with a higher Eastern Cooperative Oncology Group (ECOG) score associated with a lower proportion of patients suffering from systemic side effects was found. Women had 5.79 times higher odds to exhibit systemic ADRs after the third dose (p=0.01) compared to males. Increasing age was associated with a decreased likelihood of exhibiting ADRs (p=0.016). Conclusion:  The mRNA-1273 vaccine shows a tolerable safety profile. The likelihood of ADRs appears to be associated with gender and age. Its association with ECOG scores is less evident. Further studies are needed to elucidate this data in cancer patients.<br />Competing Interests: No competing interests were disclosed.<br /> (Copyright: © 2022 Benitez Fuentes JD et al.)

Details

Language :
English
ISSN :
2046-1402
Volume :
11
Database :
MEDLINE
Journal :
F1000Research
Publication Type :
Academic Journal
Accession number :
36636471.2
Full Text :
https://doi.org/10.12688/f1000research.110268.2