Evidence map›Paper›PMID 41934578›Full record

ArticleJournal of neuro-oncology2026

Magnetic resonance imaging-based biodistribution of theranostic AGuIX nanoparticles in the NANORAD 2 clinical trial for brain metastases.

Fabien Boux, Alexis Mercier, Daniela Talba, Jean-Yves Giraud, Sandrine Dufort, Khalide Seddik, Sylvie Grand, Mélanie Gataleta, Alexandre Leboucher, Johan Pietras and 3 more

Abstract read
In one paragraph

Article in Journal of neuro-oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Nanomedicine for Glioblastoma Therapy: Novel Insights and Future Perspectives.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    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

13 authors.

Fabien BouxNH TherAguix SA, 19 Chemin des Prés, Meylan, 38240, France. fabien.boux@gmail.com.ORCID http://orcid.org/0000-0002-3417-1313
Alexis MercierRadiotherapy Department, University of Grenoble Alps, Grenoble Alps University Hospital, Inserm UA7, Grenoble, France.
Daniela TalbaNH TherAguix SA, 19 Chemin des Prés, Meylan, 38240, France.
Jean-Yves GiraudRadiotherapy Department, University of Grenoble Alps, Grenoble Alps University Hospital, Inserm UA7, Grenoble, France.
Sandrine DufortNH TherAguix SA, 19 Chemin des Prés, Meylan, 38240, France.
Khalide SeddikNH TherAguix SA, 19 Chemin des Prés, Meylan, 38240, France.
Sylvie GrandRadiotherapy Department, University of Grenoble Alps, Grenoble Alps University Hospital, Inserm UA7, Grenoble, France.
Mélanie GataletaRadiotherapy Department, University of Grenoble Alps, Grenoble Alps University Hospital, Inserm UA7, Grenoble, France.
Alexandre LeboucherRadiotherapy Department, University of Grenoble Alps, Grenoble Alps University Hospital, Inserm UA7, Grenoble, France.
Johan PietrasRadiotherapy Department, University of Grenoble Alps, Grenoble Alps University Hospital, Inserm UA7, Grenoble, France.
Olivier De BeaumontNH TherAguix SA, 19 Chemin des Prés, Meylan, 38240, France.
Géraldine Le DucNH TherAguix SA, 19 Chemin des Prés, Meylan, 38240, France.
Camille VerryRadiotherapy Department, University of Grenoble Alps, Grenoble Alps University Hospital, Inserm UA7, Grenoble, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAGuIX nanoparticles are promising theranostic agents that selectively accumulate in brain metastases via the enhanced permeability and retention effect, potentially improving radiotherapy efficacy. This ancillary analysis of the NANORAD2 trial investigates AGuIX biodistribution in patients with multiple brain metastases undergoing whole-brain radiotherapy (WBRT).

methodsSignal enhancement (SE) maps, quantifying the relative increase in T1-weighted MRI signal intensity due to AGuIX accumulation, were generated from pre- and post-injection scans of 11 patients receiving three weekly AGuIX injections (100 mg/kg) prior to radiotherapy. SE values were measured in 14 regions of interest at one hour post-injection in all patients (n = 11), at four hours in a subset (n = 4) to assess early clearance, and at one hour after the third injection (n = 7) to evaluate long-term accumulation.

resultsAt one hour post-first injection, full-volume brain metastases showed marked SE elevation to 54.1 ± 29.5% (mean and standard deviation, n = 208 metastases), while surrounding organs exhibited transient SE (especially pituitary gland) that declined at four hours (all SE values < limit of detection, n = 11). At four hours, mean metastatic SE decreased from 33.8 ± 18.4% to 18.8 ± 16.6% (n = 54, p < 10− 10), indicating partial clearance. After three weekly injections, mean metastatic SE at one hour remained stable comparing to first injection (from 63.0% to 64.8%, n = 132), demonstrating complete inter-dose clearance with no cumulative accumulation detectable by MRI.

conclusionThis study confirms selective AGuIX accumulation in brain metastases with favorable clearance kinetics, supporting radiotherapy delivery four hours post-injection to optimize therapeutic ratio while minimizing off-target exposure.

Indexed as

Brain NeoplasmsMagnetic Resonance ImagingNanoparticlesTheranostic NanomedicineFemaleHumansMaleMiddle AgedTissue DistributionAGuIX nanoparticlesBiodistributionBrain metastasesMRIRadiosensitizerRadiotherapy

Identifiers

PMID41934578
PMCPMC13050349

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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.