Endoscopic Ultrasound-guided RadioFrequency Ablation for the Treatment Pancreatic NeuroEndocrine Neoplasms

Study Purpose

This study evaluates the possibility and the safety of performing local therapy for Pancreatic neuroendocrine neoplasms (PanNENs) using radiofrequency ablation of the tumor under ultrasonography (EUS) guidance.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Interventional
Eligible Ages 18 Years - 80 Years
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

For all patients.
  • - Age ≥18 years and <80 years.
  • - Signed written informed consent.
  • - Distance from the main pancreatic duct ≥2mm.
  • - Able to undergo endoscopic ultrasound examination.
  • - Homogeneous enhancement at contrast harmonic EUS (CH-EUS) For patients with functional pancreatic neuroendocrine neoplasms (F-PanNENs), almost all insulinomas.
  • - Definitive diagnosis of a clinical syndrome related to excessive insulin secretion fasting test, insulin blood levels, C-peptide blood levels) - Single lesion visualized at CT, and/or MRI, and/or EUS.
  • - Size < 20mm.
For patients with non functional pancreatic neuroendocrine neoplasms (NF-PanNENs)
  • - EUS fine needle biopsy (FNB) proven NF-PanNENs.
  • - 68Ga-DOTATATE PET/CT positive for a pancreatic lesion and negative for lymph nodes, liver, and other distant metastases.
  • - Hyper- or Iso-enhancing pattern at MRI and/or CT with negative lymph nodes, liver, and other distant metastases.
  • - G1 or G2 ≤ 5% on histological examination of EUS-guided biopsy samples utilizing EUS-FNB needles.
  • - Diameter between 15mm and 25mm, - Absence of symptoms.
  • - Absence of inner calcifications.

Exclusion Criteria:

  • - For all patients.
  • - Known bleeding disorder that cannot be sufficiently corrected with co-fact or fresh frozen plasma (FFP) - Use of anticoagulants that cannot be discontinued.
  • - INR >1.5 or platelet count <50.000.
  • - Previous inclusion in other studies.
  • - Pregnancy.
  • - Minimal distance from the main pancreatic duct <1mm.
  • - Inability to sign the informed consent.
  • - Heterogeneous enhancement at contrast harmonic EUS (CH-EUS) For patients with F-PanNENs (almost all insulinomas) - Diagnosis work up negative excessive hormone secretion syndrome.
  • - Multiple lesions visualized at CT, and/or MRI, and/or EUS.
  • - Size > 20mm.
  • - For patients with NF-PanNENs.
  • - G2>5% or G3 on histological examination of EUS-guided biopsy samples.
  • - Diameter <15 mm and >25 mm.
  • - Presence of symptoms.
  • - Presence of calcifications.
  • - Hypo-enhancing pattern at MRI and/or CT.
  • - 68Ga-DOTATATE PET/CT positive for lymph nodes, liver, and other distant metastasis.
  • - Diagnosis on multiple endocrine neoplasia type 1 (MEN1) syndrome or Von Hippel Lindau syndrome.
- Previous inclusion in other studies

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT03834701
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

N/A
Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

Catholic University of the Sacred Heart
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

Alberto Larghi, PhD
Principal Investigator Affiliation Fondazione Policlinico Universitario Agostino Gemelli
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Other
Overall Status Recruiting
Countries Italy
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Neuroendocrine Tumors, Neuroendocrine Carcinoma, Pancreas Neoplasm, Neuroendocrine Tumor Gastrointestinal, Hormone-Secreting
Additional Details

Pancreatic neuroendocrine neoplasms (PanNENs) are rare, but their incidence has significantly increased in the last decades. The mainstay treatment of PanNENs is surgery, which is associated with a significant benefit in term of survival but also with significant short- and long-term adverse events. Based on the above data, less invasive alternative therapeutic interventions to avoid short- and long-term adverse events of surgery are needed. In this context radiofrequency ablation has been reported to be effective in the treatment of these tumors in absence of major adverse events. However, the available studies on the matter are limited by small sample size and lack of standardized criteria for patient selection.

Arms & Interventions

Arms

Experimental: EUS guided radiofrequency ablation

Radiofrequency ablation will be performed using a system that consists of an 19-gauge needle electrode (140-cm long), a radiofrequency generator, and an inner cooling system that circulates chilled saline solution during the RFA procedure.

Interventions

Device: - EUS guided radiofrequency ablation

The EUS-RFA system (Taewoong, Seoul, Korea) utilized for EUS-RFA consists of an 19-gauge needle electrode (140-cm long), a radiofrequency generator, and an inner cooling system that circulates chilled saline solution during the RFA procedure. The inner metal part is insulated over its entire length, with the exception of the terminal 5 to 20mm for energy delivery. The needle electrode is attached to a radio frequency current generator (VIVA RF generator; Taewoong) and to a cooling pump. The generator, in addition to providing radio frequency current, allows the control of physical power and impedance parameters.

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

International Sites

Roma, RM, Italy

Status

Not yet recruiting

Address

Fondazione Policlinico Universitario Agostino Gemelli

Roma, RM, 00168

Site Contact

Carolina Gualtieri

[email protected]

00390630156580

Universita' del Sacro Cuore, Rome, Italy

Status

Recruiting

Address

Universita' del Sacro Cuore

Rome, , 00136

Site Contact

Alberto Larghi, MD

[email protected]

+390630156580

Stay Informed & Connected