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Evaluation of Thyroid Stunning From a Diagnostic Dose of I-123

Primary Purpose

Differentiated Thyroid Cancer

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
rhTSH
Sponsored by
University of Colorado, Denver
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Differentiated Thyroid Cancer focused on measuring thyroid cancer

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient must be 21-years-old or greater.
  • Patient must be status post near total thyroidectomy for differentiated thyroid cancer without known distant metastases and who are planning to undergo routine remnant thyroid tissue ablation with I-131.
  • Patients must qualify for thyroid ablation with I-131.

Exclusion Criteria:

  • Women who are pregnant or breastfeeding.
  • Prior bovine TSH use.
  • Known metastatic thyroid cancer.
  • History of cardiovascular disease that may adversely affect patient participation at the discretion of the primary investigator.
  • Patients on hemodialysis.
  • Patients with acute serious illnesses at the discretion of the primary investigator.

Sites / Locations

  • Fawn N White

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Differentiated Thyroid Cancer

Arm Description

All patients will receive one extra imaging scan with I-123 in addition to their routine care as described above. This research portion of their care will be similar to the scan that they undergo for the I-123 planning scan that is already a part of their routine care. The research study, which will be performed in the middle of the patient's normal standard of care treatment, will take 4 days. On days 1 and 2, all patients will receive a intramuscular injection of rhTSH (Thyrogen). On day 3, all patients will be given 3 mCi of I-123 in the form of a pill to take by mouth. On day 4, all patients will receive a I-123 Whole Body Imaging Scan and a thyroid camera scan of the neck and thigh.

Outcomes

Primary Outcome Measures

Difference in uptake of I-123 in the thyroid remnant in the neck in the two imaging studies.
Greater than a 20% decrease from the first to second study will indicate evidence of stunning.

Secondary Outcome Measures

Full Information

First Posted
October 27, 2014
Last Updated
October 22, 2019
Sponsor
University of Colorado, Denver
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1. Study Identification

Unique Protocol Identification Number
NCT02278198
Brief Title
Evaluation of Thyroid Stunning From a Diagnostic Dose of I-123
Official Title
Evaluation of Thyroid Stunning From a Diagnostic Dose of I-123
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
November 30, 2012 (Actual)
Primary Completion Date
September 20, 2019 (Actual)
Study Completion Date
September 20, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to find out if the small dose of radioiodine, that is used for the dosimetry study on patients with differentiated thyroid cancer, may stun the cancer cells and make the thyroid cancer treatment less effective.
Detailed Description
This study plans to learn more about a medical problem called thyroid stunning. Thyroid stunning is a temporary decrease in the function of thyroid cells after small doses of radioiodine, a radioactive drug that is commonly used to treat thyroid cancer. Thyroid stunning can be an important medical problem in patients who have thyroid cancer that has spread beyond the thyroid gland (metastases). In patients with thyroid cancer metastases, some researchers believe it is good to give the maximum safe dose of radioiodine in order to have the greatest chance of destroying the cancer. The maximum safe dose is the highest dose of radioiodine that a patient can safely receive, and this dose is unique to each person. This special personalized dose is determined by first doing a dosimetry study. Dosimetry study is a planning study that calculates the safest dose that the patient can receive. Currently, it is not known whether the small dose of radioiodine that is used for the dosimetry study may stun the cancer cells and make the thyroid cancer treatment less effective. There are two important types of radioiodine. I-123 is a form of radioiodine that is used to take pictures of the thyroid gland. I-131 is a form of radioiodine that is used to treat thyroid cancer. It is hoped that this study will produce important information that may be the first step in resolving the thyroid stunning question. Investigators will use I-123, a form of iodine that is currently not known to cause thyroid stunning, before thyroid cancer treatment with I-131. Investigators will try to prove that I-123 does not cause thyroid stunning and does not make the thyroid cancer treatment less effective. Patients are being asked to be in this research study because they have differentiated thyroid cancer, and they have no evidence of thyroid cancer that has spread to the other parts of their body. As a result, those patients thyroid cancer treatment with radioiodine will be a smaller amount than what is needed to treat patients with thyroid cancer that has spread to other parts of the body. Thyroid stunning is not a medical problem for patients like these. However, by participating in this study, the information investigators gather from those patients treatment of thyroid cancer may help those patients with thyroid cancer metastases.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Differentiated Thyroid Cancer
Keywords
thyroid cancer

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Differentiated Thyroid Cancer
Arm Type
Experimental
Arm Description
All patients will receive one extra imaging scan with I-123 in addition to their routine care as described above. This research portion of their care will be similar to the scan that they undergo for the I-123 planning scan that is already a part of their routine care. The research study, which will be performed in the middle of the patient's normal standard of care treatment, will take 4 days. On days 1 and 2, all patients will receive a intramuscular injection of rhTSH (Thyrogen). On day 3, all patients will be given 3 mCi of I-123 in the form of a pill to take by mouth. On day 4, all patients will receive a I-123 Whole Body Imaging Scan and a thyroid camera scan of the neck and thigh.
Intervention Type
Drug
Intervention Name(s)
rhTSH
Other Intervention Name(s)
Thyrogen
Intervention Description
Intramuscular injections of rhTSH (Thyrogen) will be given on days 1 and 2.
Primary Outcome Measure Information:
Title
Difference in uptake of I-123 in the thyroid remnant in the neck in the two imaging studies.
Description
Greater than a 20% decrease from the first to second study will indicate evidence of stunning.
Time Frame
11 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient must be 21-years-old or greater. Patient must be status post near total thyroidectomy for differentiated thyroid cancer without known distant metastases and who are planning to undergo routine remnant thyroid tissue ablation with I-131. Patients must qualify for thyroid ablation with I-131. Exclusion Criteria: Women who are pregnant or breastfeeding. Prior bovine TSH use. Known metastatic thyroid cancer. History of cardiovascular disease that may adversely affect patient participation at the discretion of the primary investigator. Patients on hemodialysis. Patients with acute serious illnesses at the discretion of the primary investigator.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer Kwak, MD
Organizational Affiliation
Department of Radiology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fawn N White
City
Denver
State/Province
Colorado
ZIP/Postal Code
80211
Country
United States

12. IPD Sharing Statement

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Evaluation of Thyroid Stunning From a Diagnostic Dose of I-123

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