Theranostic PET for target validation and tumor detection in solid cancers
Official title: Theranostic PET for Target Validation and Tumor Detection
Run by University Hospital, Essen · NCT07664410 · Data updated 2026-11-12
This is an observational effort to see how theranostic PET scans reflect tumor targets and help with staging, restaging, and treatment planning for adults with solid cancers.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 2000 (estimated) |
| Sponsor | University Hospital, Essen Academic / other |
| Locations | 1 site (Essen) |
| Status | Recruiting |
| Started | September 23, 2025 |
| Main results expected | September 23, 2035 |
| Study ends | September 23, 2035 |
| Registry record updated | June 24, 2026 |
| Trial ID | NCT07664410 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) with solid malignancies who are scheduled for theranostic PET as part of routine staging or restaging.
✕Probably not a fit
Patients whose tumors do not express targets detectable by theranostic PET or whose imaging does not alter management may see no direct benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Patients undergoing theranostic PET scans as part of routine cancer care are enrolled to collect data on how well PET tracer uptake matches molecular target expression, how often tumor regions show uptake, and how PET findings influence clinical decisions. The study analyzes diagnostic performance metrics such as sensitivity, specificity, PPV, and detection rate, using both PET/CT and PET/MRI with novel or established tracers. Primary endpoint examines the association between PET uptake intensity and histopathologic target expression. Secondary endpoints cover per-lesion uptake, regional and patient-level detection, and changes in staging or prognosis.
Why it matters
Potential benefit: If successful, findings could improve how PET findings guide personalized therapy and staging decisions in solid cancers.
How similar studies have gone: Previous studies in theranostic imaging have shown potential for target-guided planning, but the extent of correlation with histopathology across tumor types remains variable.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. PET imaging with a theranostic PET tracer scheduled for staging or restaging of tumor types as part of clinical routine 2. Age ≥ 18 years Exclusion Criteria: 1. Patient cannot give consent for the study 2. Patient cannot lie flat or tolerate PET imaging 3. Unwillingness or inability to comply with study and follow-up procedures 4. Condition of patient which is critical to participate in this study in the discretion of the investigators 5. Pregnant, lactating, or breast-feeding women
Where it's running
-
University Hospital Essen
Essen, Germany Recruiting
Study contacts
- Principal investigator: David Kersting, MD PhD — University Hospital, Essen
- Study coordinator: Josephine Enste
- Email: josephine.enste@uk-essen.de
- Phone: +492017232073
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.