Evidence map›Paper›PMID 35439304›Full record

ArticleCancer immunology research2022

Neoadjuvant Intravenous Oncolytic Vaccinia Virus Therapy Promotes Anticancer Immunity in Patients.

Adel Samson, Emma J West, Jonathan Carmichael, Karen J Scott, Samantha Turnbull, Bethany Kuszlewicz, Rajiv V Dave, Adam Peckham-Cooper, Emma Tidswell, Jennifer Kingston and 20 more

Abstract read
In one paragraph

Article in Cancer immunology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

  1. Trial
  2. Article
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  6. The emerging role of oncolytic virotherapy in genitourinary malignancies.Frontiers in cell and developmental biology · 2026
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Oncolytic Virotherapy in Solid Tumors: A Current Review.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

30 authors.

Adel SamsonLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0002-3081-7850
Emma J WestLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0001-7449-120X
Jonathan CarmichaelLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0001-5946-0384
Karen J ScottLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0002-5790-9579
Samantha TurnbullLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.
Bethany KuszlewiczLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.
Rajiv V DaveManchester University NHS Foundation Trust, Manchester, United Kingdom.ORCID 0000-0001-6827-8090
Adam Peckham-CooperLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.ORCID 0000-0001-5660-5314
Emma TidswellLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.
Jennifer KingstonLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Michelle JohnpulleLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Barbara da SilvaLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.
Victoria A JenningsLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.
Kaidre BendjamaTransgene, Strasbourg, France.ORCID 0000-0003-2185-9116
Nicolas StojkowitzTransgene, Strasbourg, France.
Monika LuskyTransgene, Strasbourg, France.
K R PrasadLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Giles J ToogoodLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Rebecca AuerOntario Health Research Institute, Ottawa, Canada.
John BellOntario Health Research Institute, Ottawa, Canada.ORCID 0000-0002-9083-357X
Chris J TwelvesLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0002-1849-7153
Kevin J HarringtonThe Institute of Cancer Research, London, United Kingdom.
Richard G VileMayo Clinic, Rochester, Minnesota.
Hardev PandhaUniversity of Surrey, Guildford, United Kingdom.
Fiona Errington-MaisLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0003-2155-534X
Christy RalphLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0001-5581-2987
Darren J NewtonLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0002-0214-1486
Alan Anthoney *Leeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.
Alan A Melcher *The Institute of Cancer Research, London, United Kingdom.
Fiona Collinson *Leeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0001-6964-6406

Funding

Cancer Research UKDepartment of Health
6 · The paper itself

Abstract

Improving the chances of curing patients with cancer who have had surgery to remove metastatic sites of disease is a priority area for cancer research. Pexa-Vec (Pexastimogene Devacirepvec; JX-594, TG6006) is a principally immunotherapeutic oncolytic virus that has reached late-phase clinical trials. We report the results of a single-center, nonrandomized biological end point study (trial registration: EudraCT number 2012-000704-15), which builds on the success of the presurgical intravenous delivery of oncolytic viruses to tumors. Nine patients with either colorectal cancer liver metastases or metastatic melanoma were treated with a single intravenous infusion of Pexa-Vec ahead of planned surgical resection of the metastases. Grade 3 and 4 Pexa-Vec-associated side effects were lymphopaenia and neutropaenia. Pexa-Vec was peripherally carried in plasma and was not associated with peripheral blood mononuclear cells. Upon surgical resection, Pexa-Vec was found in the majority of analyzed tumors. Pexa-Vec therapy associated with IFNα secretion, chemokine induction, and resulted in transient innate and long-lived adaptive anticancer immunity. In the 2 patients with significant and complete tumor necrosis, a reduction in the peripheral T-cell receptor diversity was observed at the time of surgery. These results support the development of presurgical oncolytic vaccinia virus-based therapies to stimulate anticancer immunity and increase the chances to cure patients with cancer.

Indexed as

Liver NeoplasmsOncolytic VirotherapyOncolytic VirusesHumansLeukocytes, MononuclearNeoadjuvant TherapyVaccinia virus

Identifiers

PMID35439304
PMCPMC9381099

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.