Ex Vivo Evaluation on Human Tissue of the Binding of Experimental Radiolabeled Ligands (HERO)

Central Hospital, Nancy, France

Status: Begins enrollment in 1 month

Conditions: Early Assessment of Tissue Uptake of Experimental Ligands

Treatments: Other: Early assessment of tissue uptake of experimental ligands

Study type: Observational

Funder types: Other

Identifiers

NCT07047677

2025PI088

Details and patient eligibility

About

The HERO project aims to structure an ex vivo screening platform, based on anonymized human tissues, to early assess the tissue fixation of experimental ligands in an ethical, translational approach that complies with the principles of the 3Rs (Replacement, Reduction, Refinement).

Full description

The development of radioligands targeting structures of diagnostic or therapeutic interest is a central challenge in nuclear medicine. However, their selection still relies primarily on animal models, which are poorly representative of human tissue, limiting clinical transposability and delaying innovation, in contradiction with the ethical principles of animal experimentation.

Recent work has highlighted the value of ex vivo approaches on human tissue to better anticipate the specificity of radioligand binding, while reducing the need for animal models. Autohistoradiography, in particular, allows precise visualization of the tissue distribution of radiolabeled molecules, without systemic interference.

The HERO project aims to structure an ex vivo screening platform, based on anonymized human tissues, to early assess the tissue fixation of experimental ligands in an ethical, translational approach that complies with the principles of the 3Rs (Replacement, Reduction, Refinement).

Enrollment: 300 estimated patients

Sex: All

Ages: 18 to 99 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients who underwent surgical resection at the Nancy University Hospital after 2019 (Information provided in the welcome booklet or on posters displayed in waiting rooms, mentioning the possible use of data or resection specimens, unless otherwise stated).
• No documented objection, in accordance with the MR004 methodology.
• Frozen human tissues (slides, blocks, or sections) from surgical resection or biopsy, transmitted by the CRB or the biopathology department.
• Samples are fully anonymized before being made available for analysis.

Exclusion criteria

• • Unusable tissue (degraded, insufficient, contaminated, poorly preserved).

  • Lack of traceability of the material.
  • Explicit opposition from the patient to the use of their tissue for research.