Movatterモバイル変換


[0]ホーム

URL:


Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
Thehttps:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

NIH NLM Logo
Log inShow account info
Access keysNCBI HomepageMyNCBI HomepageMain ContentMain Navigation
pubmed logo
Advanced Clipboard
User Guide

Full text links

Impact Journals, LLC full text link Impact Journals, LLC Free PMC article
Full text links

Actions

Review
.2026 Jan 3:17:1-29.
doi: 10.18632/oncotarget.28824.

COVID vaccination and post-infection cancer signals: Evaluating patterns and potential biological mechanisms

Affiliations
Review

COVID vaccination and post-infection cancer signals: Evaluating patterns and potential biological mechanisms

Charlotte Kuperwasser et al. Oncotarget..

Abstract

A growing number of peer-reviewed publications have reported diverse cancer types appearing in temporal association with COVID-19 vaccination or infection. To characterize the nature and scope of these reports, a systematic literature search from January 2020 to October 2025 was conducted based on specified eligibility criteria. A total of 69 publications met inclusion criteria: 66 article-level reports describing 333 patients across 27 countries, 2 retrospective population-level investigations (Italy: ~300,000 cohort, and Korea: ~8.4 million cohort) quantified cancer incidence and mortality trends among vaccinated populations, and one longitudinal analysis of ~1.3 million US miliary service members spanning the pre-pandemic through post-pandemic periods. Most of the studies documented hematologic malignancies (non-Hodgkin's lymphomas, cutaneous lymphomas, leukemias), solid tumors (breast, lung, melanoma, sarcoma, pancreatic cancer, and glioblastoma), and virus-associated cancers (Kaposi and Merkel cell carcinoma). Across reports, several recurrent themes emerged: (1) unusually rapid progression, recurrence, or reactivation of preexisting indolent or controlled disease, (2) atypical or localized histopathologic findings, including involvement of vaccine injection sites or regional lymph nodes, and (3) proposed immunologic links between acute infection or vaccination and tumor dormancy, immune escape, or microenvironmental shifts. The predominance of case-level observations and early population-level data demonstrates an early phase of potential safety-signal detection. These findings underscore the need for rigorous epidemiologic, longitudinal, clinical, histopathological, forensic, and mechanistic studies to assess whether and under what conditions COVID-19 vaccination or infection may be linked with cancer.

Keywords: COVID; cancer; carcinoma; infection; leukemia; lymphoma; sarcoma; vaccine.

PubMed Disclaimer

Conflict of interest statement

CONFLICTS OF INTEREST

W.S.E-D., co-Editor-in-Chief of Oncotarget, was not involved in the review of this manuscript or the decision to accept it.

Figures

Figure 1
Figure 1. Distribution of reported malignancies by COVID-19 vaccine type.
Distribution of vaccine formulations among vaccinated patients with reported cancer following COVID-19 immunization. Most cases involved Pfizer-BioNTech (BNT162b2; 56%) and Moderna (mRNA-1273; 25%) vaccines, followed by AstraZeneca/ChAdOx1 (Covishield; 17%) and Johnson & Johnson/Ad26.COV2.S (8%). A small fraction of reports involved Sinovac (CoronaVac), Sinopharm (BBIBP-CorV), or other inactivated vaccines, as well as unspecified mRNA or COVID-19 vaccine types. The predominance of mRNA vaccines reflects their widespread global use during the study period.
Figure 2
Figure 2. Distribution of post-vaccination and post-infection malignancies by tumor type.
Distribution of reports with malignancy or tumor-like lesions temporally associated with COVID-19 vaccination, SARS-CoV-2 infection, or SARS-CoV-2 infection and vaccination. Pie charts depict the proportional representation of major cancer categories observed. (A) Accross all studies. (B) COVID-19 vaccination, (C) SARS-CoV-2 infection, and (D) combined SARS-CoV-2 infection and COVID-19 vaccination. Cancer types were consolidated into seven high-level categories. Carcinoma includes: breast cancer, prostate cancer, colon cancer, pancreatic cancer, lung cancer, Merkel cell carcinoma, GI neoplasia/polyposis. Lymphoma also includes lymphoid neoplasms, cutaneous lymphoproliferative disorders, lymphoproliferative disorder. Other includes benign tumors, pseudotumors, mixed tumors, heart tumors, inflammatory and non-specific tumors (e.g., myofibroblastic).
Figure 3
Figure 3. Representative examples of cancers reported in temporal association with COVID-19 vaccination.
Figures were reproduced with permissions (Supplementary Table 1). Lymphoma: (A) Axillary adenopathy and i) 18-FDG-PET/CT at baseline in the right axillary adenopathy mass and ii) in multiple axillary adenopathies and subsequent NHL diagnosis following vaccination. Image reproduced from Cavanna et al., Medicina, 2023. © MDPI. (B) Temporal mass after her first BNT162b2 dose, with persistent lymphadenopathy on imaging. Axial computed tomography image shows (i, ii) submandibular and jugular regions. Image reproduced from Sekizawa et al., Front Med, 2022. © Frontiers. Sarcoma (C) High-grade sarcoma arising near injection site. A 6-cm right upper-arm mass after second Moderna dose, near the prior injection site; pathology confirmed high-grade sarcoma. Image adapted with permission from Bae et al., Cureus, 2023 © Springer Nature. (D) Classic cutaneous Kaposi’s sarcoma adapted from Li et al. Front Med, 2022 © Frontiers. A 79-year-old man developed violaceous papules on the legs after the first ChAdOx1 vaccine dose; biopsy confirmed KS. Treatment included radiotherapy and doxorubicin. Clinical images of Kaposi sarcoma (i) with dark brown macules over the left foot, (ii) the right foot and larger reddish erythematous papules on his left calf (iii, iv). Carcinoma (E) In a 96-patient cohort, repeated booster vaccination correlated with poorer overall survival and elevated IgG4 level of pancreatic ductal adenocarcinoma. Kaplan–Meier analysis of 96 PC patients with known vaccination history and measured IgG4 levels, total IgG4 levels by number of vaccinations, and Kaplan–Meier analysis in PC patients by IgG4 levels. Image adapted with permission from Abue et al. Cancers 2025 © MDPI. (F) A case of metastatic breast carcinoma to the skin expressing SARS-CoV-2 spike protein. Histopathology of skin metasstatis along with IHC for nucleocapsid and Spike protein. Images adapted from Sano, S., J. Derm Sci, 2025. © Elsevier. Melanoma (G) Gross examination of specimen shows extensive intraocular hemorrhage involving both anterior and posterior chambers, accompanied by complete retinal detachment. H&E stained section shows severely degenerated, necrotic melanocytic lesion located with widespread necrosis within the melanocytic tumor. SOX10 IHC confirms melanocytic cells containing cytoplasmic melanin, interspersed among numerous SOX10-negative melanophages. Image adapted with permission from Wagle et al. Indian J Ophthalmo 2022 © Wolters Kluwer. (H) Maximum-intensity projection PET image shows markedly increased radiotracer uptake within the left axillary and supraclavicular lymph nodes. Representative axial CT and corresponding fused PET/CT images highlight the dominant nodal conglomerate. The patient had received a COVID-19 vaccination in the left upper arm within two months prior to imaging. Image adapted from Gullotti et al. Radiol Case Rep. 2022 © Elsevier. Glioblastoma (I) Two patients (ages 40 and 31) presented with new neurologic deficits and frontal-lobe masses shortly after mRNA vaccination. Image adapted from O’Sullivan et al. J of Neurology. 2021 © Elsevier. Other (J) Gastrointestinal polyposis identified following COVID-19 vaccination. Image adapted with permission from Kim et al. Clin Endosc 2024 © Korean Society of Gastrointestinal Endoscopy (K) Axillary lymphangioma in an 80-year-old woman three months after her second Pfizer-BioNTech dose; imaging showed a cystic lymphangioma. Image adapted with permission from Sasa et al. Surg Case Rep 2022 © Springer Nature.
Figure 4
Figure 4. Annual incidence rates of non-Hodgkin lymphoma (NHL) subtypes among active-component U.S. service members, 2017–2023.
Figure adapted from Russell et al. [85] using Defense Medical Surveillance System data demonstrating rise in specified/unspecified NHL and mature T/NK-cell subtypes. Vertical lines denote key timepoints: the onset of the COVID-19 pandemic (early 2020) and the beginning of the Department of Defense vaccine mandate (late 2020–early 2021).
Figure 5
Figure 5. Proposed mechanism of tumor hyperprogression following COVID-19 vaccination.
(A) Conceptual model illustrating how inoculation with mRNA vaccine leads to immune reactions depending on its biodistribution. Strong immunostimulation can override immunosurveillance of latent cancer cells and trigger tumor hyperprogression. (B) Schematic representation of the major immune cell types influencing tumor growth and immune regulation following mRNA vaccine exposure. LNP–encapsulated modified mRNA (modRNA/mRNA) interacts with innate immune sensors altering cytokine signaling (TNF-α, IL-1β, IL-6) and immune-cell polarization leading to immunosuppression and reduced cytotoxic CD8+ T-cell activity. Expansion of myeloid suppressor populations, along with pro-tumor cytokine feedback loops, fosters accelerated tumor cell proliferation and immune evasion. The imbalance between anti-tumor (M1, CD8+, NK) and pro-tumor (M2, Treg, MDSC) networks favors tumor hyperprogression.
See this image and copyright information in PMC

References

    1. Saha A, Ghosh Roy S, Dwivedi R, Tripathi P, Kumar K, Nambiar SM, Pathak R. Beyond the Pandemic Era: Recent Advances and Efficacy of SARS-CoV-2 Vaccines Against Emerging Variants of Concern. Vaccines (Basel). 2025; 13:424. 10.3390/vaccines13040424. - DOI - PMC - PubMed
    1. Chakraborty C, Lo YH, Bhattacharya M, Das A, Wen ZH. Looking beyond the origin of SARS-CoV-2: Significant strategic aspects during the five-year journey of COVID-19 vaccine development. Mol Ther Nucleic Acids. 2025; 36:102527. 10.1016/j.omtn.2025.102527. - DOI - PMC - PubMed
    1. Kumar A, Ahmad F, Sah BK, Aljabali AAA, Mishra Y, Mishra V. Advancements in viral vaccine development: from traditional to modern approaches. Explor Immunol. 2025; 5:1003203. 10.37349/ei.2025.1003203. - DOI
    1. Papadatou I, Michos A. Advances in Biotechnology and the Development of Novel Human Vaccines. Vaccines (Basel). 2025; 13:989. 10.3390/vaccines13090989. - DOI - PMC - PubMed
    1. Yang D, Tian J, Shen C, Li Q. An overview and single-arm meta-analysis of immune-mediated adverse events following COVID-19 vaccination. Front Pharmacol. 2024; 15:1308768. 10.3389/fphar.2024.1308768. - DOI - PMC - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources

Full text links
Impact Journals, LLC full text link Impact Journals, LLC Free PMC article
Cite
Send To

NCBI Literature Resources

MeSHPMCBookshelfDisclaimer

The PubMed wordmark and PubMed logo are registered trademarks of the U.S. Department of Health and Human Services (HHS). Unauthorized use of these marks is strictly prohibited.


[8]ページ先頭

©2009-2026 Movatter.jp