Evidence map›Paper›PMID 42621760›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Toward Personalized Theranostics: A Modular PET Platform for Antibody-Based Imaging and Therapy.

Delphine Vivier, Megane Grah Kple, Julen Ariztia, Marion Leroux, Mathieu Moreau, Michael Claron, Maxime Cheveau, Adam Laouafa, Agnieszka Kownacka, Camille Petitot and 7 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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

17 authors.

Delphine VivierCNRS, ICMUB UMR 6302, Université Bourgogne Europe, Dijon, France.ORCID https://orcid.org/0000-0002-7903-2819
Megane Grah KpleCNRS, ICMUB UMR 6302, Université Bourgogne Europe, Dijon, France.
Julen AriztiaCNRS, ICMUB UMR 6302, Université Bourgogne Europe, Dijon, France.
Marion LerouxCNRS, ICMUB UMR 6302, Université Bourgogne Europe, Dijon, France.ORCID https://orcid.org/0009-0004-5889-6652
Mathieu MoreauCNRS, ICMUB UMR 6302, Université Bourgogne Europe, Dijon, France.ORCID https://orcid.org/0000-0003-1429-8461
Michael ClaronCNRS, ICMUB UMR 6302, Université Bourgogne Europe, Dijon, France.
Maxime CheveauCNRS, ICMUB UMR 6302, Université Bourgogne Europe, Dijon, France.
Adam LaouafaCNRS, ICMUB UMR 6302, Université Bourgogne Europe, Dijon, France.
Agnieszka KownackaCentre Georges-François Leclerc-Unicancer, INSERM, BioSanD US 58, Plateforme IMATHERA, Université Bourgogne Europe, Dijon, France.
Camille PetitotCentre Georges-François Leclerc-Unicancer, INSERM, BioSanD US 58, Plateforme IMATHERA, Université Bourgogne Europe, Dijon, France.
John SimonetCentre Georges-François Leclerc-Unicancer, INSERM, BioSanD US 58, Plateforme IMATHERA, Université Bourgogne Europe, Dijon, France.
Alexandre M M DiasCentre Georges-François Leclerc-Unicancer, INSERM, BioSanD US 58, Plateforme IMATHERA, Université Bourgogne Europe, Dijon, France.ORCID https://orcid.org/0000-0002-9241-1231
Sophie PotyCNRS, ICMUB UMR 6302, Université Bourgogne Europe, Dijon, France.
Charles TruilletCEA, CNRS, Inserm, BioMaps, Université Paris-Saclay, Orsay, France.
Bertrand CollinCNRS, ICMUB UMR 6302, Université Bourgogne Europe, Dijon, France.
Alexandra OudotCentre Georges-François Leclerc-Unicancer, INSERM, BioSanD US 58, Plateforme IMATHERA, Université Bourgogne Europe, Dijon, France.
Franck DenatCNRS, ICMUB UMR 6302, Université Bourgogne Europe, Dijon, France.ORCID https://orcid.org/0000-0002-9652-4006

Funding

European Regional Development Fund projectCOMETEFrench National Institute of Cancer INCA 16409
6 · The paper itself

Abstract

The expansion of personalized medicine is encouraging the development of platforms capable of supporting individualized imaging and therapeutic strategies. The combination of antibodies, with their intrinsic selectivity, and a modular molecular probe provides a strong foundation for such approaches. In this context, a versatile platform enabling positron emission tomography (PET) imaging followed by copper-free click-based functionalization is developed. A DFO-Lysine-DBCO probe is synthesized and site-specifically coupled to trastuzumab, allowing the introduction of diverse payloads, including β- or α-emitter chelators, a fluorophore, and a cytotoxic agent. Within this toolbox, the DFO/DOTAGA bischelate is selected for detailed evaluation. Radiolabeling confirms the selectivity of DFO and DOTAGA for

Indexed as

bischelate immunoconjugatecopper‐free click chemistrymodular antibody platformPET/SPECT imagingsite‐specific conjugationtargeted therapytheranostics

Identifiers

PMID42621760
PMCPMC13491523

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.