Evidence map›Paper›PMID 42213481›Full record

ReviewBJS open2026

Cancer vaccines: comprehensive review.

Rachael E Clifford, Nichola Manu, Qian Yang, Zeeshan Arif, David Aggen, Michael E Bryan, Aditi Gupta, Heather Shaw, David Church, Philippa Corrie and 4 more

Abstract readReview
In one paragraph

Review in BJS open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Rachael E CliffordColorectal and Peritoneal Oncology Centre (CPOC), The Christie NHS Foundation Trust, Manchester, UK.ORCID 0000-0001-7065-0197
Nichola ManuThe Liverpool Head and Neck Centre, The University of Liverpool, Liverpool, UK.
Qian YangCentre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Zeeshan ArifColorectal and Peritoneal Oncology Centre (CPOC), The Christie NHS Foundation Trust, Manchester, UK.
David AggenGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Centre, New York, New York, USA.
Michael E BryanCentre for Immuno-Oncology, University of Oxford, Oxford, UK.
Aditi GuptaGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Centre, New York, New York, USA.
Heather ShawDepartment of Medical Oncology, University College London Hospital, London, UK.
David ChurchCentre for Immuno-Oncology, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Philippa CorrieCambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Natalia SavelyevaThe Liverpool Head and Neck Centre, The University of Liverpool, Liverpool, UK.
Christian OttensmeierThe Liverpool Head and Neck Centre, The University of Liverpool, Liverpool, UK.
Sarah DansonDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.ORCID 0000-0002-3593-2890
Robert JonesThe Liverpool Head and Neck Centre, The University of Liverpool, Liverpool, UK.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundThere has been an increasing focus on the potential of cancer vaccines as a therapeutic oncological option, aiming to harness the immune system to recognize and eliminate malignant cells. Unlike traditional therapies, vaccines exploit tumour-associated antigens and neoantigens to generate durable, tumour-specific immune responses.

methodsThis review provides a comprehensive overview of current vaccine strategies, their clinical applications, and implications for surgical oncology.

resultsClinical trials highlight promising results in high-mutational burden cancers such as melanoma, lung, and bladder cancer, as well as in traditionally 'cold' tumours like pancreatic cancer. Combination strategies, particularly with checkpoint inhibitors, have shown enhanced efficacy, exemplified by messenger RNA-4157/V940 and autogene cevumeran in adjuvant settings. Off-the-shelf tumour-associated antigen vaccines offer scalability but face challenges of tolerance and limited specificity. Early data suggest vaccines may improve relapse-free survival and induce antigen spreading, broadening immune responses beyond the initial targets.

conclusionCancer vaccines are poised to complement surgery and systemic therapies, particularly in the perioperative window. Their integration into multimodal treatment strategies may redefine precision oncology, offering durable disease control and improved patient outcomes.

Indexed as

Cancer VaccinesNeoplasmsAntigens, NeoplasmHumansImmunotherapyAntigens, NeoplasmCancer Vaccines

Identifiers

PMID42213481
PMCPMC13220758

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.