An Initial Study of Lithium in Patients With Medullary Thyroid Cancer

Medullary Thyroid Cancer Clinical Trial

Official title:

An Initial Study of Lithium in Patients With Medullary Thyroid Cancer

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00582712
• Other study ID #: CO07312
• Secondary ID: 2007-0195NCI-201
• Status: Terminated
• Phase: Phase 2
• Start date: January 2008
• Est. completion date: April 2012

Study information

• Verified date: October 2016
• Source: University of Wisconsin, Madison
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Primary objective is to evaluate the tumor response rate of patients with MTC treated with Lithium carbonate

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 5
• Est. completion date: April 2012
• Est. primary completion date: May 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically confirmed MTC with signs of residual/persistent disease based on tumor marker levels and/or radiographic imaging. Pathologic diagnosis must be confirmed at UWCCC. Grading must be confirmed by pathologic review performed at UWCCC.

• Elevated neuroendocrine markers at least 1 month post -op. In MTC, persistently elevated neuroendocrine markers such as calcitonin and CEA are indicative of persistent disease.

• Disease progression is not required for this trial

• 4 weeks from the completion of major surgery, chemotherapy, or other systemic therapy or local liver therapy to study registration. Subjects will have had standard of care prior to enrollment. Subjects will have had standard of care prior to enrollment (for example it could include total thyroidectomy, central lymph node dissection, and when necessary ipsilateral radical neck dissection but is tailored to the patient).

• 3 weeks from the completion of radiation therapy to study registration

• The following laboratory values obtained within 14 days prior to registration:

• Absolute neutrophils count (ANC) = 1000/mm3

• Platelets = 75,000/mm3

• Hemoglobin = 8.0 g/dL

• Total bilirubin greater than or equal to 2.0 X the upper limit of normal (ULN)

• AST greater than or equal to 3 X ULN or greater than or equal to 5 X ULN if liver metastases are present

• Creatinine greater than or equal to ULN

• Serum sodium within normal limits

• ECOG performance status of 2

• Capable of understanding the investigational nature, potential risks and benefits of the study, and able to provide valid informed consent.

• Availability of tissue specimens to be analyzed for pathologic confirmation.

• Age = 18 years.

• Women must not be pregnant or lactating due to the deleterious effects of Lithium carbonate on a fetus or small child. All females of childbearing potential must have a blood test or urine study within 2 weeks prior to registration to rule out pregnancy.

• Women of childbearing potential and sexually active males are required to use an accepted and effective method of contraception.

• Patients must not have known history of allergic reactions or adverse reactions to Lithium or its derivatives.

• Patients are not allowed to be on concurrent chemotherapy or radiation therapy.

Exclusion Criteria:

• Gastrointestinal tract disease resulting in an inability to take oral medication (i.e. ulcerative disease, uncontrolled nausea, vomiting, diarrhea, bowel obstruction, or inability to swallow the tablets).

• Significant, active cardiac disease

• Patients must not be taking the following medications: diuretics, ACE inhibitors, NSAIDs (except aspirin or sulindac), neuroleptics, tetracycline, and COX2 inhibitors.

• Patients with radiographic evidence of disease will be presented the option to undergo a tumor biopsy although this is not mandatory.

• Patients already taking Lithium for any reason are not allowed on study

Related Conditions & MeSH terms

• Carcinoma, Neuroendocrine
• Medullary Thyroid Cancer
• Thyroid Diseases
• Thyroid Neoplasms

Intervention

Drug:
• Lithium carbonate
Lithium 300mg by mouth, three times daily, escalating to a lithium level of 0.8-1.2; Continue until progressive disease/unacceptable toxicity; Evaluate every 4 weeks.

Locations

Country	Name	City	State
United States	Uniersity of Wisconsin Comprehensive Cancer Center	Madison	Wisconsin

Sponsors (1)

Lead Sponsor	Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tumor Response Rate Measured by the Response Evaluation Criteria in Solid Tumors (RECIST)		1 year

External Links

•   University of Wisconsin Carbone Cancer Center