Conn Syndrome, Endoscopic Ultrasound (EUS), Insulinoma; Pancreas, MEN1, NETs, Radiofrequency Ablation
Conditions
Brief summary
The goal of this observational study is to evaluate the long-term clinical effectiveness of EUS-RFA and quality of life in patients with pancreatic or adrenal tumors recieving EUS-RFA. Primary Objectives: * Clinical effectiveness: To evaluate the proportion of included patients who show doc-umented improvement in their clinical symptoms and biochemical parameters (blood test results) over time. * Patient satisfaction: To assess patient satisfaction with the procedure and subsequent disease-related quality of life, measured using validated questionnaires. Secondary Objectives: * Safety: To determine the proportion of treated patients who experience complications, as defined by the AGREE classification, within 30 days after the procedure. * Technical success: To assess the proportion of included patients in whom the EUS-RFA procedure can be successfully completed. Exploratory Objectives: • To identify factors associated with adverse events and factors related to clinical success or lack there of. The study is observational. All participant will receive EUS-RFA as part of their standard clinical care. Participants will: * Undergo EUS-RFA, in which a fine needle is guided into the tumor using an endo-scope and ultrasound imaging. Radiofrequency energy is applied through the needle to heat and destroy tumor cells while protecting the surrounding tissue. * Have follow-up visits including blood tests, imaging scans, and clinical evaluations at regular intervals for up to 5 years after treatment. * Complete validated questionnaires about satisfaction and quality of life. The study will include approximately 138 patients recruited between 2025 and 2035 from two Danish hospital departments (Herlev and Gentofte Hospital and Rigshospitalet). Data collection will continue until 2040 to assess long-term outcomes. This study may help determine whether EUS-RFA can serve as a safe and effective alternative to traditional surgery for selected patients with small hormone-producing or benign tumors in the pancreas or adrenal glands, potentially reducing surgical risks and improving recovery and quality of life.
Interventions
OTHERobservational study
Observational study. Patients recieve standard clinical care with routine follow up
Sponsors
Herlev Hospital
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients with one or more lesions amendable to undergo EUS-RFA * Insulinomas ≤ 25 mm confirmed by a 72-h fasting test, cross-sectional scanning, and a biopsy with low Ki67 index (\<10%) * Non-functional pNEN lesions between 10-20 mm and growing, confirmed by a biopsy with low Ki67 index (\<10%), or larger pNEN lesions in patients who are not candidates for surgical treatment * Unilateral APA with benign characteristics on non-contrast enhanced CT located in the left adrenal and confirmed lateralization on AVS * Adult habile patients * Signed informed consent
Exclusion criteria
* Severe multimorbidity (ASA score ≥ IV or ECOG performance score ≥ 4) * Uncorrected coagulopathy (INR \>1.8 or thrombocyte count \< 50 mia/L) * Pregnancy * Metastatic malignancy with expected remaining life expectancy \< 3 years * Stenosis in upper GI tract or altered anatomy (e.g. previous gastrectomy) preventing the passage of an echoendoscope
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Patient satisfaction | From enrollment and 5 years forward | Patient satisfaction measured through validated questionarie SF-36. Scores for each domain range from 0 to 100, with a higher score defining a more favorable state |
| Clinical efficacy | From enrollment and 5 years forward | Proportion of included patients with documented biochemical response and symptom improvement, or lesion size decrement/cessation of growth in case of MEN1 patients |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Adverse events | From enrollment and 5 years forward | Proportion of treated patients experiencing AEs as defined by AGREE classification during a 30-day period following the procedure |
| Technical success | From enrollment and 5 years forward | Proportion of included patients where EUS-RFA was technically feasible |
Other
| Measure | Time frame | Description |
|---|---|---|
| Factors associated with clinical success or failure | From enrollment and 5 years forward | Factors associated with clinical success or failure |
| Factors associated with adverse events | From enrollment and 5 years forward | Factors associated with adverse events |
Countries
Denmark
Contacts
Primary ContactBojan Kovacevic, ph.d., MD
Backup ContactLouise Maegaard, MSc, RN
Outcome results
None listed