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Immunogenicity of SARS-CoV-2 messenger RNA vaccines in patients with cancer.
Literature Information
| DOI | 10.1016/j.ccell.2021.06.009 |
|---|---|
| PMID | 34214473 |
| Journal | Cancer cell |
| Impact Factor | 44.5 |
| JCR Quartile | Q1 |
| Publication Year | 2021 |
| Times Cited | 156 |
| Keywords | COVID-19, anti-cancer treatment, antibody, immune response, malignancy |
| Literature Type | Journal Article |
| ISSN | 1535-6108 |
| Pages | 1091-1098.e2 |
| Issue | 39(8) |
| Authors | Alfredo Addeo, Pankil K Shah, Natacha Bordry, Robert D Hudson, Brenna Albracht, Mariagrazia Di Marco, Virginia Kaklamani, Pierre-Yves Dietrich, Barbara S Taylor, Pierre-Francois Simand, Darpan Patel, Jing Wang, Intidhar Labidi-Galy, Sara Fertani, Robin J Leach, Jose Sandoval, Ruben Mesa, Kate Lathrop, Nicolas Mach, Dimpy P Shah |
TL;DR
This study investigates the efficacy of SARS-CoV-2 mRNA vaccines in cancer patients, revealing that 94% of the 131 participants achieved seroconversion after two doses, though those with hematological malignancies had significantly lower rates and antibody responses. The findings underscore the need for tailored vaccination strategies in cancer patients, particularly for those receiving certain treatments, to enhance their immune response against SARS-CoV-2.
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COVID-19 · anti-cancer treatment · antibody · immune response · malignancy
Abstract
Patients with cancer experience a higher burden of SARS-CoV-2 infection, disease severity, complications, and mortality, than the general population. SARS-CoV-2 mRNA vaccines are highly effective in the general population; however, few data are available on their efficacy in patients with cancer. Using a prospective cohort, we assessed the seroconversion rates and anti-SARS-CoV-2 spike protein antibody titers following the first and second dose of BNT162b2 and mRNA-1273 SARS-CoV-2 vaccines in patients with cancer in US and Europe from January to April 2021. Among 131 patients, most (94%) achieved seroconversion after receipt of two vaccine doses. Seroconversion rates and antibody titers in patients with hematological malignancy were significantly lower than those with solid tumors. None of the patients with history of anti-CD-20 antibody in the 6 months before vaccination developed antibody response. Antibody titers were highest for clinical surveillance or endocrine therapy groups and lowest for cytotoxic chemotherapy or monoclonal antibody groups.
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Primary Questions Addressed
- What specific factors contribute to the lower seroconversion rates observed in patients with hematological malignancies compared to those with solid tumors?
- How do different cancer treatments, such as cytotoxic chemotherapy and monoclonal antibodies, impact the immunogenic response to SARS-CoV-2 mRNA vaccines?
- What are the long-term implications of lower antibody titers in cancer patients post-vaccination for their overall health and COVID-19 risk?
- Are there any specific recommendations for vaccination strategies in cancer patients to enhance immunogenicity and protect against SARS-CoV-2?
- How does the timing of vaccination in relation to cancer treatment affect the immune response to mRNA vaccines in patients with cancer?
Key Findings
Research Background and Objectives
Patients with cancer are at a higher risk of severe outcomes from COVID-19. This study aimed to assess the immunogenicity of SARS-CoV-2 mRNA vaccines (BNT162b2 and mRNA-1273) in cancer patients, focusing on seroconversion rates and antibody titers after vaccination. The goal was to determine how effective these vaccines are in generating an immune response in this vulnerable population.
Main Methods/Materials/Experimental Design
A prospective cohort study was conducted involving 140 cancer patients from the US and Switzerland who received either BNT162b2 or mRNA-1273 vaccines between January and April 2021. The study assessed seroconversion rates and anti-SARS-CoV-2 spike protein IgG antibody titers at two time points: after the first and second vaccine doses.
Experimental Design Overview
Key Results and Findings
- Seroconversion Rates: 94% of patients achieved seroconversion after the second dose, compared to 81% after the first dose.
- Antibody Titers: Patients with solid tumors had significantly higher antibody titers than those with hematological malignancies.
- Non-responders: 6% of patients (mostly with hematological malignancies) did not develop antibodies post-vaccination, particularly those treated with anti-CD-20 therapies.
- Impact of Treatment: Patients undergoing cytotoxic chemotherapy had lower antibody titers compared to those on clinical surveillance or endocrine therapy.
Main Conclusions/Significance/Innovation
The study confirms that most cancer patients develop a robust antibody response to mRNA COVID-19 vaccines, particularly after the second dose. However, it highlights the concern for specific subgroups, such as those with hematological malignancies or those receiving immunosuppressive treatments, who may not respond adequately to vaccination. This underscores the need for tailored vaccination strategies and potential booster doses for immunocompromised patients.
Research Limitations and Future Directions
- Limitations: The study did not assess cellular immunity, which is critical for understanding overall vaccine efficacy. Additionally, the sample size for certain demographics was small, limiting generalizability.
- Future Directions: Further research is needed to evaluate the cellular immune response in this population and to explore the effectiveness of additional vaccine doses or alternative vaccination strategies for high-risk groups.
| Aspect | Details |
|---|---|
| Study Design | Prospective cohort study, assessing mRNA vaccine response in cancer patients |
| Population | 140 cancer patients (131 analyzed for immunogenicity) |
| Key Findings | 94% seroconversion after second dose; lower response in hematological malignancies and certain therapies |
| Limitations | Lack of cellular immunity data; small sample size for some demographics |
| Future Research Needs | Explore cellular immunity and optimal vaccination strategies for immunocompromised patients |
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