Evidence map›Paper›PMID 42330421›Full record

ArticleCancer discovery2026

Deconvolving SARS-CoV-2 mRNA vaccine impact on immunotherapy-related survival.

Justin Jee, Jiajia Zhang, Jessica A Lavery, Michele Waters, Christoper J Fong, Andy J Minn, Michael S Glickman, Katherine S Panageas, Charles L Sawyers, Nikolaus Schultz

Abstract read
PubMed Publisher
In one paragraph

Article in Cancer discovery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Interpreting vaccine-associated survival differences in immune checkpoint inhibitor therapy.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Justin JeeMemorial Sloan Kettering Cancer Center New York United States.ORCID 0000-0001-9783-0139
Jiajia ZhangMemorial Sloan Kettering Cancer Center New York United States.ORCID 0009-0002-3012-5050
Jessica A LaveryMemorial Sloan Kettering Cancer Center New York, New York United States.ORCID 0000-0002-2746-5647
Michele WatersMemorial Sloan Kettering Cancer Center New York, NY United States.ORCID 0000-0002-5416-5172
Christoper J FongMemorial Sloan Kettering Cancer Center New York, NY United States.ORCID 0000-0002-8929-1478
Andy J MinnMemorial Sloan Kettering Cancer Center New York United States.ORCID 0000-0003-1418-0906
Michael S GlickmanMemorial Sloan Kettering Cancer Center New York United States.ORCID 0000-0001-7918-5164
Katherine S PanageasMemorial Sloan Kettering Cancer Center New York United States.ORCID 0000-0002-6591-604X
Charles L SawyersMemorial Sloan Kettering Cancer Center New York, NY United States.ORCID 0000-0003-4955-6475
Nikolaus SchultzMemorial Sloan Kettering Cancer Center New York, NY United States.ORCID 0000-0002-0131-4904

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Project 3: Predictors of sensitivity to immunotherapy and targeted treatments based on real world evidenceP01CA275746 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CHARLES L. SAWYERS · 2024 to 2026
$9.4M
NCI NIH HHS P01 CA275746NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Real-world data suggest that SARS-CoV-2 mRNA vaccines, administered within 100 days of immune checkpoint inhibitor (ICI) treatment ("peri-ICI vaccination"), may improve ICI effectiveness through synergistic immune priming. In an independent real-world cohort and re-analysis of a published cohort, both from tertiary cancer centers in the USA, multiple analyses did not support a treatment-synergy hypothesis. Applying a prior analytic framework, although longer survival with peri-ICI vaccination was observed at the start of the pandemic, this association was not seen in periods when vaccination was broadly available. Longer survival with vaccination in the early pandemic was also not specific to ICI therapies. Progression-free survival during periods of high vaccine uptake was not longer than in pre-vaccination periods. Together, these findings indicate that the previously reported vaccination survival advantage is largely explained by selection bias, with patients who had more favorable prognoses more likely to receive SARS-CoV-2 vaccination, particularly in the early pandemic.

Identifiers

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.