Immunogenicity and risk of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection after Coronavirus Disease 2019 (COVID-19) vaccination in patients with cancer: a systematic review and meta-analysis

被引:98
作者
Becerril-Gaitan, Andrea [1 ]
Vaca-Cartagena, Bryan F. [1 ]
Ferrigno, Ana S. [1 ]
Mesa-Chavez, Fernanda [1 ]
Barrientos-Gutierrez, Tonatiuh [2 ]
Tagliamento, Marco [3 ,4 ]
Lambertini, Matteo [4 ,5 ]
Villarreal-Garza, Cynthia [1 ]
机构
[1] Tecnol Monterrey, Breast Canc Ctr, Hosp Zambrano Hell TecSalud, San Pedro Garza Garcia, Nuevo Leon, Mexico
[2] Ctr Populat Hlth Res, Natl Inst Publ Hlth, Cuernavaca, Morelos, Mexico
[3] IRCCS Osped Policlin San Martino, Dept Med Oncol, Med Oncol 2, Genoa, Italy
[4] Univ Genoa, Dept Internal Med & Med Specialties DiMI, Genoa, Italy
[5] IRCCS Osped Policlin San Martino, Dept Med Oncol, UOC Clin Oncol Med, Genoa, Italy
关键词
Neoplasms; Haematologic neoplasms; COVID-19; vaccines; SARS-CoV-2; Immunogenicity; Vaccines; breakthrough infections; VACCINES;
D O I
10.1016/j.ejca.2021.10.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Patients with cancer are considered a priority group for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) vaccination given their high risk of contracting severe Coronavirus Disease 2019 (COVID-19). However, limited data exist regarding the efficacy of immunisation in this population. In this study, we assess the immunologic response after COVID-19 vaccination of cancer versus non-cancer population. Methods: PubMed, Cochrane Central Register of Controlled Trials (CENTRAL), and Web of Science databases were searched from 01st March 2020 through 12th August 12 2021. Primary end-points were anti-SARS-CoV-2 spike protein (S) immunoglobulin G (IgG) seroconversion rates, T-cell response, and documented SARS-CoV-2 infection after COVID-19 immunisation. Data were extracted following the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines. Overall effects were pooled using random-effects models. Results: This systematic review and meta-analysis included 35 original studies. Overall, 51% (95% confidence interval [CI], 41-62) and 73% (95% CI, 64-81) of patients with cancer devel-oped anti-S IgG above the threshold level after partial and complete immunisation, respec-tively. Patients with haematologic malignancies had a significantly lower seroconversion rate than those with solid tumours after complete immunisation (65% vs 94%; P < 0.0001). Compared with non-cancer controls, oncological patients were less likely to attain seroconver-sion after incomplete (risk ratio [RR] 0.45 [95% CI 0.35-0.58]) and complete (RR 0.69 [95% CI 0.56-0.84]) COVID-19 immunisation schemes. Patients with cancer had a higher likeli-hood of having a documented SARS-CoV-2 infection after partial (RR 3.21; 95% CI 0.35-29.04) and complete (RR 2.04; 95% CI 0.38-11.10) immunisation. Conclusions: Patients with cancer have an impaired immune response to COVID-19 vaccina-tion compared with controls. Strategies that endorse the completion of vaccination schemes are warranted. Future studies should aim to evaluate different approaches that enhance onco-logical patients' immune response. 2021 Elsevier Ltd. All rights reserved.
引用
收藏
页码:243 / 260
页数:18
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