Evidence map›Paper›PMID 39785814›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2025

A Phase I Clinical Trial of Intrahepatic Artery Delivery of TG6002 in Combination with Oral 5-Fluorocytosine in Patients with Liver-Dominant Metastatic Colorectal Cancer.

Emma J West, Alain Sadoun, Kaidre Bendjama, Philippe Erbs, Cristina Smolenschi, Philippe A Cassier, Thierry de Baere, Sophie Sainte-Croix, Maud Brandely, Alan A Melcher and 14 more

Abstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Review
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  5. Article
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  7. Review
  8. Review
  9. Oncolytic viruses: advanced strategies in cancer therapy.Signal transduction and targeted therapy · 2026
    Review
  10. Article
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  12. Review
  13. Article
  14. Article
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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

24 authors.

Emma J WestLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0001-7449-120X
Alain SadounTransgene, Illkirch-Graffenstaden, France.ORCID 0009-0007-7721-6714
Kaidre BendjamaTransgene, Illkirch-Graffenstaden, France.ORCID 0000-0003-2185-9116
Philippe ErbsTransgene, Illkirch-Graffenstaden, France.ORCID 0000-0002-6810-4610
Cristina SmolenschiInstitut Gustave Roussy, Villejuif, France.ORCID 0000-0002-7568-6196
Philippe A CassierMedical Oncology, Centre Léon Bérard, Lyon, France.ORCID 0000-0003-3857-1688
Thierry de BaereInstitut Gustave Roussy, Villejuif, France.ORCID 0000-0002-4556-7663
Sophie Sainte-CroixTransgene, Illkirch-Graffenstaden, France.ORCID 0009-0007-3866-0724
Maud BrandelyTransgene, Illkirch-Graffenstaden, France.ORCID 0009-0005-6058-1681
Alan A MelcherThe Institute of Cancer Research, London, United Kingdom.ORCID 0000-0002-2042-3380
Fay IsmailLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0009-0003-2171-5523
Karen J ScottLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0002-5790-9579
Angela BennettLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.ORCID 0009-0002-8834-8695
Emma BanksLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.ORCID 0009-0001-7076-7667
Ewa GasiorLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.ORCID 0009-0004-8056-024X
Sarah KentLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.ORCID 0009-0004-7350-7934
Marta KurzawaLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.ORCID 0009-0008-7567-3441
Christopher HammondLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.ORCID 0000-0001-9435-5678
Jai V PatelLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.ORCID 0000-0001-9248-0125
Fiona J CollinsonLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0001-6964-6406
Chris TwelvesLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0002-1849-7153
D Alan AnthoneyLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0001-5695-8312
Dan SwinsonLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.ORCID 0000-0002-6186-5759
Adel SamsonLeeds Institute of Medical Research at St. James's, University of Leeds, Leeds, United Kingdom.ORCID 0000-0002-3081-7850

Funding

Cancer Research UK (CRUK) 29039Transgene
6 · The paper itself

Abstract

purposeEffective treatment for patients with metastatic cancer is limited, particularly for those with colorectal cancer with metastatic liver lesions, in which accessibility to numerous tumors is essential for favorable clinical outcomes. Oncolytic viruses (OV) selectively replicate in cancer cells; however, direct targeting of inaccessible lesions is limited when using conventional intravenous or intratumoral administration routes. PATIENTS AND

methodsWe conducted a multicenter, dose-escalation, phase I study of vaccinia virus, TG6002, via intrahepatic artery (IHA) delivery in combination with the oral prodrug 5-fluorocytosine to 15 patients with metastatic colorectal cancer.

resultsSuccessful IHA delivery of replication-competent TG6002 was achieved, as demonstrated by the virus within tumor biopsies. Functional transcription of the FCU1 transgene indicates viral replication within the tumor, with higher plasma 5-fluorouracil associated with patients receiving the highest dose of TG6002. IHA delivery of TG6002 correlated with a robust systemic peripheral immune response to the virus with activation of peripheral blood mononuclear cells, associated with a proinflammatory cytokine response and release of calreticulin, potentially indicating immunogenic cell death. Gene Ontology analyses of differentially expressed genes reveal a significant immune response at the transcriptional level in response to treatment. Moreover, an increase in the number and frequency of T-cell receptor clones against both cancer antigens and neoantigens, with elevated functional activity, may be associated with improved anticancer activity. Despite these findings, no clinical efficacy was observed.

conclusionsIn summary, these data demonstrate the delivery of OV to tumor via IHA administration, associated with viral replication and significant peripheral immune activation. Collectively, the data support the need for future studies using IHA administration of OVs.

Indexed as

Colorectal NeoplasmsFlucytosineLiver NeoplasmsOncolytic VirotherapyVaccinia virusAdministration, OralAdultAgedCombined Modality TherapyFemaleHepatic ArteryHumansMaleMiddle AgedOncolytic VirusesTreatment OutcomeFlucytosine

Identifiers

PMID39785814
PMCPMC11959272

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.