Pioglitazone in Thyroid Cancers

NCT01655719 | Completed Phase 2 Results DMC FDA Drug

• 2 other identifiers: 2011.097R01CA166033
• Study Type: interventional
• Target: 1
• Locations: 1 country
• Sites: 4

Brief Summary

Through this trial the investigators hope to learn if a drug, Actos (pioglitazone), is useful in treating a certain kind of metastatic thyroid cancer. Actos is approved by the FDA to treat diabetes. It has not been approved by the FDA to treat cancer, so its use in this study is considered experimental.

Conditions

Thyroid Cancers That Contain the PAX8-PPARgamma Fusion Gene

Outcome Measures

Primary Outcomes (1)

• Tumor Response (Change)

  Response is measured by change in Tumor size (cm)

  Baseline and 24 weeks

Secondary Outcomes (2)

• Change in Serum Thyroglobulin

  Baseline and 24 weeks

• Toxicity

  24 weeks

Other Outcomes (3)

• Biomarkers

  24 weeks

• Sensitization to Radioiodine Therapy

  24 weeks

• Lipid Accumulation in Tumor

  24 weeks

Study Arms (1)

Pioglitazone Treatment

EXPERIMENTAL

If eligible, subjects can participate in 1 or both parts of this study as follows: Part 1: In the initial main portion of the study subjects will receive 24 -28 weeks of therapy with pioglitazone at the dosage approved for the control of diabetes. Response will be evaluated per RECIST. Safety measure are outlined in the protocol including weekly weigh ins, calls, labs, exams, etc. Part 2: A secondary protocol is then available to subjects who complete the main initial study with less than complete response per RECIST. They can undergo a radioiodine scan to see if the treatment with pioglitazone has sensitized their disease to radioiodine. If it has - they can pursue the radioiodine treatment.

Drug: Pioglitazone

Interventions

Pioglitazone DRUG

Also known as: Actos

Pioglitazone Treatment

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients must have histologically confirmed thyroid carcinoma with the PAX8-PPARgamma translocation (translocation testing will be performed on archived tissue during the screening period).
• Refractory to radioactive iodine (RAI) as defined by: the tumor does not concentrate RAI; or the patient has had RAI within the last 16 months and has had progression despite that RAI; or the last RAI treatment was \>16 months ago and the patient progressed after at least two RAI treatments; or the patient has received RAI treatments with a cumulative RAI dose of ≥22.2 GBq (600 mCi)
• Not a candidate for surgery or RAI therapy with curative intent.
• Lesions that would be treated by external beam radiation therapy (EBRT) based on standard of care can be so treated, but then cannot be used as target lesions.
• Measurable disease by RECIST 1.1 criteria.
• Documented disease progression by RECIST 1.1 in the past 14 months.
• Availability of histological material (primary tumor or metastases) for review of the diagnosis and demonstration of PAX8-PPARgamma fusion gene.
• Adequate TSH suppression (\<0.5 mIU/L)
• Prior chemotherapy or surgery must have been completed at least 28 days prior to registration, and all toxicities must have resolved.
• Prior radioactive iodine must have been completed at least 6 months prior to registration, or there must be documented disease progression since such therapy if it was within 6 months. Sites that have received EBRT must have disease progression post-EBRT to be used as sites of measurable disease.
• Life expectancy of greater than 6 months.
• ECOG performance status 2 or less.
• Patients must have normal organ function as defined below:
• AST(SGOT)/ALT(SGPT) less than 2.5 X institutional upper limit of normal (within 1 month of study Day 1)
• Patients must be able to consume oral medications.

You may not qualify if:

• Patients may not be receiving any other investigational agents.
• Patients with known untreated brain metastases.
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to pioglitazone.
• Diagnosis of diabetes mellitus or current therapy with any drugs used to treat diabetes mellitus, including but not limited to insulin, sulfonylureas, metformin, rosiglitazone (Avandia), and pioglitazone (Actos) within 14 days of study Day 1
• Therapy with rosiglitazone (Avandia) or pioglitazone (Actos) at any time since the diagnosis of thyroid cancer.
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, congestive heart failure, unstable angina pectoris, or cardiac arrhythmias.
• Pregnant women are excluded from this study because pioglitazone is a U.S. Food and Drug Administration Pregnancy Category C drug. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with pioglitazone, breastfeeding should be discontinued if the mother is treated with pioglitazone.
• No concurrent radiotherapy or chemotherapy may be given to the patient during the administration of the study drug.
• Patients with uncontrolled malabsorption syndromes.
• Patients with a history of congestive heart failure of any New York Heart Association class.
• Any medical or psychiatric illness which, in the opinion of the principal investigator, would compromise the patient's ability to tolerate this treatment regimen.
• Use of rifampin (strong CYP2C8 inducer) within 14 days of study Day 1.
• Other current malignancy than the disease under study.
• Grade 2 or worse edema within 14 days of study Day 1, per CTCAE v4.

Sponsors & Collaborators

• University of Michigan: lead
• National Cancer Institute (NCI): collaborator

Study Sites (4)

University of Colorado

Aurora, Colorado, 80045, United States

Location

University of Michigan

Ann Arbor, Michigan, 48109, United States

Location

University of Pennsylvania

Philadelphia, Pennsylvania, 19104, United States

Location

University of Texas MD Anderson Cancer Center

Houston, Texas, 77030, United States

Location

Related Publications (1)

• Giordano TJ, Haugen BR, Sherman SI, Shah MH, Caoili EM, Koenig RJ. Pioglitazone Therapy of PAX8-PPARgamma Fusion Protein Thyroid Carcinoma. J Clin Endocrinol Metab. 2018 Apr 1;103(4):1277-1281. doi: 10.1210/jc.2017-02533.

  PMID: 29373711 DERIVED

MeSH Terms

Interventions

Pioglitazone

Intervention Hierarchy (Ancestors)

Thiazolidinediones; Thiazoles; Sulfur Compounds; Organic Chemicals; Azoles; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds

Results Point of Contact

• Title: Tim Muth
• Organization: University of Michigan

tmuth@med.umich.edu

734-615-8914

Study Officials

• Ronald J Koenig, MD, PhD

  University of Michigan

  PRINCIPAL INVESTIGATOR

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: No

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: July 25, 2012
• First Posted: August 2, 2012
• Study Start: April 1, 2012
• Primary Completion: March 31, 2017
• Study Completion: March 31, 2017
• Last Updated: October 26, 2017
• Results First Posted: October 26, 2017

Record last verified: 2017-09

Locations

US (4)