Evidence map›Paper›PMID 42350043›Full record

ArticleJournal for immunotherapy of cancer2026

COVID-19 mRNA vaccination and immune-related adverse events in patients with cancer receiving immune checkpoint inhibitors: a target trial emulation study.

Po-Huang Chen, Wei-Cheng Chang, Hong-Jie Jhou, Hsin-Yu Chen, Li-Ting Kao, Tina Yi-Jin Hsieh, Ming-Shen Dai, Cho-Hao Lee

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2026. 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. Review
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

8 authors.

Po-Huang Chen *Department of Oncology, Tri-Service General Hospital, National Defense Medical University, Taipei, Taiwan.ORCID http://orcid.org/0000-0002-0280-6417
Wei-Cheng Chang *Department of Ophthalmology, Universal Eye Center, Taipei, Taiwan.
Hong-Jie JhouNeurological Institute, Changhua Christian Hospital, Changhua, Taiwan.
Hsin-Yu ChenDepartment of Family Medicine, Chi Mei Medical Center, Tainan, Taiwan.
Li-Ting KaoGraduate Institute of Life Sciences, National Defense Medical University, Taipei, Taiwan.
Tina Yi-Jin HsiehDepartment of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Ming-Shen DaiDepartment of Oncology, Tri-Service General Hospital, National Defense Medical University, Taipei, Taiwan.
Cho-Hao LeeDepartment of Oncology, Tri-Service General Hospital, National Defense Medical University, Taipei, Taiwan drleechohao@gmail.com.ORCID http://orcid.org/0000-0002-6061-5168

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCOVID-19 messenger RNA (mRNA) vaccines enhance immune checkpoint inhibitor (ICI) efficacy through type I interferon responses, but may theoretically increase the burden of immune-related adverse events (irAEs). This study aimed to determine whether vaccination increases irAE risk in patients with ICI-treated cancer and to quantify the balance between toxicity and survival benefits.

methodsWe conducted a retrospective cohort study using target trial emulation methodology within the TriNetX Research Global Network (January 2021 to December 2025). We identified 7,218 adult patients with metastatic cancer initiating ICI therapy. Patients who received COVID-19 mRNA vaccination within 100 days before ICI initiation (n=3,609) were matched 1:1 to unvaccinated controls (n=3,609) using propensity scores. The primary outcome was the composite incidence of irAEs at 36 months. Secondary outcomes included severe irAEs, organ-specific irAEs, all-cause mortality, and intensive care unit (ICU) admission. Probabilistic quantitative bias analysis (VanderWeele-Ding formulation) and a composite ocular negative-control outcome (incident age-related cataract and glaucoma) were used to assess robustness to unmeasured confounding and differential ophthalmological surveillance.

resultsVaccinated patients had a significantly increased risk of overall irAEs compared with unvaccinated controls (HR 1.22, 95% CI 1.17 to 1.28; E-value 1.74). This increase included clinically significant severe irAEs (HR 1.11, 95% CI 1.04 to 1.18). Organ-specific analyses revealed that the overall increase was primarily driven by ocular irAEs (HR 1.48, 95% CI 1.17 to 1.87), with non-significant trends for dermatologic and rheumatologic irAEs. However, vaccination was associated with substantial survival benefits, including 14% lower all-cause mortality (HR 0.86, 95% CI 0.80 to 0.93) and 57% fewer ICU admissions (HR 0.43, 95% CI 0.25 to 0.73). Point estimates were numerically higher in females and patients aged ≥50 years, although tests for interaction were not statistically significant.

conclusionsCOVID-19 mRNA vaccination is associated with a modest but clinically meaningful 22% increase in irAEs, driven largely by ocular manifestations. However, the substantial survival benefits clearly outweigh these toxicity risks. Vaccination should continue in all eligible patients, with enhanced monitoring recommended for irAEs, particularly ophthalmological surveillance for high-risk groups.

Indexed as

COVID-19COVID-19 VaccinesImmune Checkpoint InhibitorsNeoplasmsAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesSARS-CoV-2VaccinationCOVID-19 VaccinesImmune Checkpoint InhibitorsImmune Checkpoint InhibitorsImmunotherapy

Identifiers

PMID42350043
PMCPMC13311639

What OpenQuestion holds

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Registered trials

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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.