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Antibody response to three-dose anti-SARS-CoV-2 mRNA-vaccination in treated solid cancer patients.

Authors :
Dalu D
Tarkowski M
Ruggieri L
Cona MS
Gabrieli A
De Francesco D
Fasola C
Ferrario S
Gambaro A
Masedu E
Parma G
Rulli E
De Stradis C
Mavilio D
Calcaterra F
Manoni F
Riva A
La Verde N
Source :
International journal of cancer [Int J Cancer] 2024 Apr 15; Vol. 154 (8), pp. 1371-1376. Date of Electronic Publication: 2023 Dec 15.
Publication Year :
2024

Abstract

Solid cancer patients are at higher risk of SARS-CoV-2 infection and severe complications. Moreover, vaccine-induced antibody response is impaired in patients on anticancer treatment. In this retrospective, observational, hypothesis-generating, cohort study, we assessed the antibody response to the third dose of mRNA vaccine in a convenience sample of patients on anticancer treatment, comparing it to that of the primary two-dose cycle. Among 99 patients included, 62.6% were ≥60 years old, 32.3% males, 67.7% with advanced disease. Exactly 40.4% were receiving biological therapy, 16.2% chemotherapy only and 7.1% both treatments. After the third dose, seroconversion rate seems to increase significantly, especially in non-responders to two doses. Heterologous vaccine-type regimen (two-dose mRNA-1273 and subsequent tozinameran or vice versa) results in higher antibody levels. This explorative study suggests that repeated doses of mRNA-vaccines could be associated with a better antibody response in this population. Furthermore, heterologous vaccine-type three-dose vaccination seems more effective in this population. Since this is a hypothesis-generating study, adequately statistically powered studies should validate these results.<br /> (© 2023 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.)

Details

Language :
English
ISSN :
1097-0215
Volume :
154
Issue :
8
Database :
MEDLINE
Journal :
International journal of cancer
Publication Type :
Academic Journal
Accession number :
38100252
Full Text :
https://doi.org/10.1002/ijc.34817