Pioglitazone Hydrochloride in Treating Patients With Stage IA-IIIA Non-small Cell Lung Cancer

National Cancer Institute (NCI)

Status and phase: Terminated; Phase 2

Conditions: Stage IA Non-Small Cell Lung Carcinoma; Stage IIA Non-Small Cell Lung Carcinoma; Stage IIB Non-Small Cell Lung Carcinoma; Stage IB Non-Small Cell Lung Carcinoma; Stage IIIA Non-Small Cell Lung Cancer

Treatments: Drug: Pioglitazone Hydrochloride; Other: Quality-of-Life Assessment; Other: Laboratory Biomarker Analysis

Study type: Interventional

Funder types: NIH

Identifiers

NCT01342770

P30CA015083 (U.S. NIH Grant/Contract)

MAY10-15-02 (Other Identifier)

N01-CN-2012-00042

N01CN35000 (U.S. NIH Grant/Contract)

MAYO-MAY10-15-02

NCI-2011-03826 (Registry Identifier)

CDR0000699459

N01CN00042 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This pilot phase II trial studies how well pioglitazone works in treating patients with stage IA-IIIA non-small cell lung cancer. Pioglitazone hydrochloride may slow the growth of tumor cells and may be an effective treatment for non-small cell lung cancer.

Full description

PRIMARY OBJECTIVES:

I. To evaluate the mechanism(s) of action of pioglitazone as a candidate chemopreventive agent for lung cancer by investigating the effects on Ki-67 defined in non-small cell lung cancer (NSCLC) tumor tissue.

SECONDARY OBJECTIVES:

I. To determine the effects of pioglitazone on multiple markers listed below:

• Tumor tissue: caspase-3, cyclin D1, p21/Waf1, peroxisome proliferative activated receptor, gamma (PPARγ), mucin 1 (MUC1).
• Premalignant tissue: Ki-67, caspase-3, PPARγ.
• Histologically normal tissue: Ki-67, PPARγ. II. To evaluate the toxicity and safety of pioglitazone in this patient population.

III. To analyze the expression of serum markers that are affected by pioglitazone.

IV. To describe the effects of limited treatment with pioglitazone on tumor metabolic activity as determined by FDG-PET (assessed before and after a minimum of 2 weeks of treatment).

OUTLINE:

Patients receive pioglitazone hydrochloride orally (PO) once daily (QD) for 14-42 days. Patients then undergo surgery.

Enrollment: 6 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Suspected or biopsy-proven NSCLC

• Willingness to provide biopsy tissue for correlative studies

• Candidate for pulmonary resection; must be able to schedule >= 14 days and =< 42 days between registration and surgery to allow for treatment with pioglitazone

• Ability to understand and the willingness to sign a written informed consent document

• Ability and willingness to swallow oral tablets

• Ability and willingness to undergo two bronchoscopies (before treatment and at the time of surgery)

  • For those participants who are undergoing mediastinoscopy as part of their standard-of-care, the pre-treatment bronchoscopy may be performed during the mediastinoscopy; if the participant remains eligible for definitive surgical resection after the mediastinoscopy, the participant may proceed to registration and pioglitazone treatment

• Current or former smoker with a >= 10 pack-year smoking history

• Women of child-bearing potential and men who agree to use adequate contraception for the duration of study participation; women must not be pregnant or lactating; women of child-bearing potential (women considered not of childbearing potential if they are at least two years postmenopausal and/or surgically sterile) must have used adequate contraception (abstinence; barrier methods such as intrauterine device [IUD], diaphragm with spermicidal gel, condom, or others; and hormonal methods such as birth control pills or others) since her last menses prior to study entry; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her study physician immediately

Exclusion criteria

• Receiving any other investigational agents
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to pioglitazone
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
• Pregnant or lactating woman
• Currently treated diabetes
• Participants with >= class II New York Heart Association (NYHA) congestive heart failure or history of congestive heart failure
• Participants with >= grade 2 (moderate) edema
• Participants currently receiving an inhibitor of cytochrome P450 family 2, subfamily C, polypeptide 8 (CYP2C8) (gemfibrozil, ketoconazole, quercetin, trimethoprim), or an inducer of CYP2C8 (cortisol, dexamethasone, phenobarbital, rifampin), or cytochrome P450 family 3, subfamily A, polypeptide 4 (CYP3A4) substrate
• Prior neoadjuvant therapy for NSCLC
• History of bladder cancer or in situ bladder cancer

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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6 participants in 1 patient group

Treatment (pioglitazone hydrochloride)

Experimental group

Description:

Patients receive pioglitazone hydrochloride PO QD for 14-42 days. Patients then undergo surgery.

Treatment:

Other: Quality-of-Life Assessment

Drug: Pioglitazone Hydrochloride

Other: Laboratory Biomarker Analysis