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Molecular-Guided Surgery for Pancreatic and GI Neuroendocrine Cancers

Primary Purpose

Neuroendocrine Carcinoma of Pancreas, Carcinoid

Status
Withdrawn
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Gallium Dotatate
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neuroendocrine Carcinoma of Pancreas focused on measuring Gallium-DOTATATE (68), Neuroendocrine Tumors, Pancreatic neuroendocrine Tumors, Molecular, Surgery, Carcinoid

Eligibility Criteria

19 Years - 100 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. At least 19 years of age and older
  2. Male or female patient with a suspected diagnosis of a gastrointestinal-pancreatic neuroendocrine tumor (localized or metastatic) to undergo surgery for resection
  3. Localization of the tumor with a pre-operative 68Gallium-DOTATATE scan
  4. In the Investigator's judgement, participant is mentally competent to provide informed consent to participate in the study.
  5. ECOG performance status of 0-1
  6. Negative urine pregnancy test at screening, if applicable.

Exclusion Criteria:

  1. Participants who are pregnant, lactating, or intending to become pregnant during the study
  2. Female participants of child-bearing age who refuse a urine pregnancy test
  3. Participants who, in the opinion of the Investigator, should not be included in the study for any reason, including inability to follow study procedures.
  4. Participants who have participated in an investigational surgical, drug, or device study within the past 30 days.
  5. Mental condition rendering the subject unable to understand the nature, scope, and possible consequences of the study.
  6. Patients whose tumors do not localize on a 68Gallium-DOTATATE scan

Sites / Locations

  • UAB Kirklin Clinic

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Gallium Dotatate

Arm Description

All patients in the study will be undergoing both a 68Gallium-DOTATATE scan for tumor localization and planned surgical resection. Both of these maneuvers are clinically indicated and the standard of care in the care of these patients. Following induction of general endotracheal anesthesia (as required for the surgery portion of treatment), the patients will receive an additional injection of 68Gallium-DOTATATE in the operating room itself. A probe that can detect 68Gallium will be used to identify tumors in the OR within the patient's abdominal cavity for targeted resection.

Outcomes

Primary Outcome Measures

Comparison of intraoperative findings to preoperative PET scan findings
PET probes will be used to quantify the level of gallium dotatate in the tumor tissue and be compared to the gallium dotatate uptake of the preoperative PET scan.

Secondary Outcome Measures

Determine threshold levels of gallium dotatate uptake in order to determine tumor involvement
Using a high energy PET probe the level of gallium uptake will be compared to histopathology analysis of removed specimen

Full Information

First Posted
August 7, 2018
Last Updated
September 6, 2023
Sponsor
University of Alabama at Birmingham
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1. Study Identification

Unique Protocol Identification Number
NCT03623984
Brief Title
Molecular-Guided Surgery for Pancreatic and GI Neuroendocrine Cancers
Official Title
Molecular-Guided Surgery for Pancreatic and Gastrointestinal Neuroendocrine Cancers
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Withdrawn
Why Stopped
no partipants
Study Start Date
June 7, 2019 (Actual)
Primary Completion Date
June 7, 2022 (Actual)
Study Completion Date
June 7, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alabama at Birmingham

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to see if the use of 68Gallium- positron emission tomography and computer tomography (PET/CT) scans along with NETSPOT® (Advanced Accelerator Applications USA, Inc.) can better define the localization of Neuroendocrine tumors enhancing the surgical removal of Neuroendocrine tumors (NETs).
Detailed Description
A challenge during cancer surgery is determining all sites of malignant disease. Accurate tumor localization is of utmost importance as complete resection increases the chance of cure and improves patient outcomes even when cure is not possible. However, finding the primary tumor can be very challenging and, in some cases, impossible. With the recent FDA approval of a PET tracer (Ga-68 DOTATATE) that binds to somatostatin receptors for imaging neuroendocrine tumors (NETs), the investigator's institution has the opportunity to dramatically improve the surgical care for these patients. Therefore, the aim for this study is to develop a molecular image-guided surgery program starting with GI NETs. GI NETs are malignant neoplasms that are increasing in prevalence. NETs cause a variety of debilitating symptoms, and, as a result, contribute substantially to cancer-related morbidity. Since the primary treatment for NET is surgical resection, NETs are an ideal model to launch a comprehensive image-guided surgery program. Many NETs are metastatic at presentation or will develop metastases during their course, and it is difficult to identify all disease visually and through manual palpation. Failure to surgically resect all disease leads to symptoms, metastatic disease, and multiple surgical interventions. Many institutions have recently begun using Ga-68 DOTATATE for PET/CT imaging of NETs, and this same tracer can be used for intra-operative localization of primary NETs as well as metastases. The primary impediment to using Ga-68 DOTATATE for this purpose is the need to develop and validate a high-energy gamma (HEG) probe for detecting NETs during surgery. This study will explore the new PET tracer technology and begin a molecular image-guided surgery program for NETs. This initial paradigm will be used to develop a molecular image guided approach to other cancers. It is expected that this type of program could usher a new era of cancer management at the investigator's institution at its forefront and improve outcomes for study participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neuroendocrine Carcinoma of Pancreas, Carcinoid
Keywords
Gallium-DOTATATE (68), Neuroendocrine Tumors, Pancreatic neuroendocrine Tumors, Molecular, Surgery, Carcinoid

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Gallium Dotatate
Arm Type
Experimental
Arm Description
All patients in the study will be undergoing both a 68Gallium-DOTATATE scan for tumor localization and planned surgical resection. Both of these maneuvers are clinically indicated and the standard of care in the care of these patients. Following induction of general endotracheal anesthesia (as required for the surgery portion of treatment), the patients will receive an additional injection of 68Gallium-DOTATATE in the operating room itself. A probe that can detect 68Gallium will be used to identify tumors in the OR within the patient's abdominal cavity for targeted resection.
Intervention Type
Drug
Intervention Name(s)
Gallium Dotatate
Other Intervention Name(s)
Gallium-DOTATATE (68)
Intervention Description
Radioguided Surgery for Pancreatic- Neuroendocrine Cancers
Primary Outcome Measure Information:
Title
Comparison of intraoperative findings to preoperative PET scan findings
Description
PET probes will be used to quantify the level of gallium dotatate in the tumor tissue and be compared to the gallium dotatate uptake of the preoperative PET scan.
Time Frame
From initial PET scan (2-3 weeks) until completion of the surgery
Secondary Outcome Measure Information:
Title
Determine threshold levels of gallium dotatate uptake in order to determine tumor involvement
Description
Using a high energy PET probe the level of gallium uptake will be compared to histopathology analysis of removed specimen
Time Frame
From baseline through 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: At least 19 years of age and older Male or female patient with a suspected diagnosis of a gastrointestinal-pancreatic neuroendocrine tumor (localized or metastatic) to undergo surgery for resection Localization of the tumor with a pre-operative 68Gallium-DOTATATE scan In the Investigator's judgement, participant is mentally competent to provide informed consent to participate in the study. ECOG performance status of 0-1 Negative urine pregnancy test at screening, if applicable. Exclusion Criteria: Participants who are pregnant, lactating, or intending to become pregnant during the study Female participants of child-bearing age who refuse a urine pregnancy test Participants who, in the opinion of the Investigator, should not be included in the study for any reason, including inability to follow study procedures. Participants who have participated in an investigational surgical, drug, or device study within the past 30 days. Mental condition rendering the subject unable to understand the nature, scope, and possible consequences of the study. Patients whose tumors do not localize on a 68Gallium-DOTATATE scan
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sushanth Reddy, MD
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
UAB Kirklin Clinic
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Molecular-Guided Surgery for Pancreatic and GI Neuroendocrine Cancers

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