Evidence map›Paper›PMID 41143943›Full record

ArticleEJNMMI research2025

Bimodality imaging as a companion to evaluate antitumour efficacy of TH-302 in experimental chondrosarcoma.

Roxane Autissier, Guilhem Pagés, Erwan Boutault, Jean-Marie Bonny, Sébastien Schmitt, Philippe Auzeloux, Yannick Bidet, Flora Ponelle-Chachuat, Aurélie Dutour, Elisabeth Miot-Noirault and 1 more

Abstract read
In one paragraph

Article in EJNMMI research, 2025. 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

11 authors.

Roxane AutissierMolecular Imaging and theranostic, Université Clermont Auvergne, INSERM, U1240, Clermont-Ferrand, F-63000, France.ORCID http://orcid.org/0000-0001-5522-6814
Guilhem PagésINRAE, UR QuaPA, Saint-Genès-Champanelle, F-63122, France.ORCID http://orcid.org/0000-0001-9368-5237
Erwan BoutaultMolecular Imaging and theranostic, Université Clermont Auvergne, INSERM, U1240, Clermont-Ferrand, F-63000, France.
Jean-Marie BonnyINRAE, UR QuaPA, Saint-Genès-Champanelle, F-63122, France.ORCID http://orcid.org/0000-0003-2858-7459
Sébastien SchmittMolecular Imaging and theranostic, Université Clermont Auvergne, INSERM, U1240, Clermont-Ferrand, F-63000, France.ORCID http://orcid.org/0000-0002-8468-6788
Philippe AuzelouxMolecular Imaging and theranostic, Université Clermont Auvergne, INSERM, U1240, Clermont-Ferrand, F-63000, France.ORCID http://orcid.org/0000-0003-2066-3904
Yannick BidetMolecular Imaging and theranostic, Université Clermont Auvergne, INSERM, U1240, Clermont-Ferrand, F-63000, France.ORCID http://orcid.org/0000-0002-9624-8195
Flora Ponelle-ChachuatMolecular Imaging and theranostic, Université Clermont Auvergne, INSERM, U1240, Clermont-Ferrand, F-63000, France.ORCID http://orcid.org/0000-0002-3637-5504
Aurélie DutourTeam Cell Death and Pediatric Cancer, Cancer Initiation and Tumour Cell Identity Department, Cancer Research Center of Lyon, Lyon, INSERM1052, CNRS5286, F-69008, France.ORCID http://orcid.org/0000-0001-5741-3576
Elisabeth Miot-NoiraultMolecular Imaging and theranostic, Université Clermont Auvergne, INSERM, U1240, Clermont-Ferrand, F-63000, France.ORCID http://orcid.org/0000-0002-8372-6602
Leslie MazuelMolecular Imaging and theranostic, Université Clermont Auvergne, INSERM, U1240, Clermont-Ferrand, F-63000, France. leslie.mazuel@uca.fr.ORCID http://orcid.org/0000-0002-0180-871X

Funding

Ligue Contre le Cancer RAB20018CCA
6 · The paper itself

Abstract

backgroundThe hypoxic status of cancer tumour is disparate within tumour microenvironment and is considered as the main cause of treatment resistance. Chondrosarcoma, a type of bone cancer, combines heterogonous tumour microenvironment and resistance to therapies. We aimed to image tumour microenvironment response to hypoxia activated prodrug therapy with Evofosfamide (TH-302) on a rat chondrosarcoma model thanks to an original multimodal imaging strategy. Bimodal imaging strategy consisted of nuclear imaging and MRI on TH-302 treated and control animals. To monitor TH-302 effects on tumour growth and structure, we measured T2 and ADC by MRI and we used

resultsTH-302 demonstrated a strong efficacy on tumour structure with a reduction of its volume of 75% at the end of the protocol, a modification of the tumour microstructures and a decreased of both cellularity and cell proliferation. The drug also modified the tumour metabolisms as shown by

conclusionsTH-302 shows an in vivo anti-tumour activity in chondrosarcoma. Our multimodal imaging approach allows monitoring complex exchanges between tumour cells and their neighboring under therapy.

Indexed as

CEST MRIChondrosarcomaEvosfosfamideNuclear imagingTumour microenvironment

Identifiers

PMID41143943
PMCPMC12559538

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.