Evidence map›Paper›PMID 41693712›Full record

ArticleFrontiers in immunology2025

Long-term cellular and humoral responses to SARS-CoV-2 vaccinations in patients with solid malignancies undergoing chemotherapy.

Andrew Liu, Brian Necela, Zhuo Li, Davitte Cogen, Mikolaj A Wieczorek, Ashita Mummareddy, Marites Acampora, Gina A Reynolds, Pooja P Advani, Alvaro Moreno-Aspitia and 7 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Andrew LiuDivision of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, FL, United States.
Brian NecelaDepartment of Cancer Biology, Mayo Clinic, Jacksonville, FL, United States.
Zhuo LiDivision of Quantitative Health Science, Mayo Clinic, Jacksonville, FL, United States.
Davitte CogenDepartment of Cancer Biology, Mayo Clinic, Jacksonville, FL, United States.
Mikolaj A WieczorekDivision of Quantitative Health Science, Mayo Clinic, Jacksonville, FL, United States.
Ashita MummareddyDivision of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, FL, United States.
Marites AcamporaDivision of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, FL, United States.
Gina A ReynoldsDivision of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, FL, United States.
Pooja P AdvaniDivision of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, FL, United States.
Alvaro Moreno-AspitiaDivision of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, FL, United States.
Melanie D SwiftDepartment of Preventive, Occupational and Aerospace Medicine, Mayo Clinic, Jacksonville, FL, United States.
Abinash VirkDivision of Infectious Disease, Mayo Clinic, Jacksonville, FL, United States.
Adil E BharuchaDivision of Gastroenterology & Hepatology, Mayo Clinic, Jacksonville, FL, United States.
Christopher P MarquezDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Jacksonville, FL, United States.
Tushar C PatelDivision of Gastroenterology & Hepatology, Mayo Clinic, Jacksonville, FL, United States.
Keith L KnutsonDepartment of Immunology, Mayo Clinic, Jacksonville, FL, United States.
Saranya ChumsriDivision of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, FL, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: While SARS-CoV-2 vaccines are highly effective in healthy individuals, the magnitude and durability of humoral and cellular responses in patients with solid malignancies receiving chemotherapy remain understudied. Previous reports suggest that patients with cancer may not mount adequate immune response after SARS-CoV-2 vaccination. Additionally, most studies focused on humoral responses, while data regarding cellular immune responses are scarce. In this study, we evaluated humoral and cellular responses in patients with solid tumors receiving chemotherapy compared to healthy individuals up to one year after vaccinations. Methods: Patients aged ≥18 who were willing to receive the SARS-CoV-2 vaccine were enrolled. Anti-SARS-CoV-2 immunoassays were used to detect antibodies against nucleocapsid and spike proteins. Human IFN-γ Fluorospot assay was used to determine antigen-specific T-cell responses. Data were compared between groups using Mann-Whitney test for continuous variables and Fisher's exact test for categorical variables. Results: A total of 67 subjects (47 patients with cancer and 20 healthy individuals) were included. 1-3 months following the second vaccine doses, 96% of patients with cancer and 100% of healthy individuals demonstrated a positive humoral response. While the positivity rate was not significantly different, patients with cancer had significantly lower spike IgG antibodies than healthy individuals. However, this difference diminished at 6 months when patients with cancer had increased antibodies compared to decreased antibodies in the healthy cohort and no difference was noticed at 12-month. Patients with cancer developed a similar antigen-specific T-cell response as healthy individuals at 1-3 months, 6 months and 12 months. There were no significant differences when comparing patients aged ≤ 55 years vs. >55 years, stages I-III vs. IV, single vs. multiple chemotherapy, and BNT162b2 vs. mRNA-1273 vaccines. There was a significant moderate correlation between neutralization and antibody levels at 12 months. However, despite patients with cancer having a significantly higher COVID risk score, there were no significant differences in COVID-19 infection and hospitalization between patients with cancer and healthy individuals. Conclusion: Despite initial impaired antibody responses to SARS-CoV-2 vaccinations, patients with solid malignancies receiving chemotherapy effectively generated long-term cellular and humoral responses by 6 and 12 months, leading to similar infection and hospitalization rates compared to healthy individuals.

Indexed as

Antineoplastic AgentsCOVID-19COVID-19 VaccinesImmunity, CellularImmunity, HumoralNeoplasmsSARS-CoV-2AdultAgedAntibodies, ViralBNT162 VaccineFemaleHumansMaleMiddle AgedT-LymphocytesAntibodies, ViralAntineoplastic AgentsBNT162 VaccineCOVID-19 Vaccineschemotherapyhumoral and cellular responses to routine vaccinesmagnitude and durabilitypatients with solid tumorsSARS-CoV-2 vaccines

Identifiers

PMID41693712
PMCPMC12894236

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.