Azacitidine in Treating Patients With Previously Treated Advanced Non-Small Cell Lung Cancer

NCT ID: NCT01281124

Last Updated: 2019-09-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 1 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-01-12
• Study Completion Date: 2012-09-12

Brief Summary

This phase II clinical trial is studying how well azacitidine works in treating patients with previously treated advanced non-small cell lung cancer. Drugs used in chemotherapy, such as azacitidine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing.

Detailed Description

PRIMARY OBJECTIVES:

I. To determine the ability of 5-azacytidine to cause DNA hypomethylation and re-expression of silenced tumor suppressor genes when stratified for high or low expression of mir29a, b, and c.

SECONDARY OBJECTIVES:

I. To compare the molecular studies (mir29 expression and tumor suppressor gene methylation) between archival tissue, fresh biopsy pre-treatment samples, and post-treatment fresh samples.

II. To determine the overall response rate by CT (RECIST 1.1 criteria) and PET (EORTC PET response criteria), PFS, and OS of patients treated with azacytidine in the second- or third-line setting.

III. To correlate the blood microRNA profiles (and changes in microRNA profiles) with response to azacytidine.

OUTLINE:

Patients receive azacitidine subcutaneously on days 1-7. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Patients undergo tissue and blood sample collection at baseline and periodically during study treatment for correlative studies. After completion of study treatment, patients are followed up for 12 weeks.

Conditions

Recurrent Lung Non-Small Cell Carcinoma; Stage IV Lung Non-Small Cell Cancer AJCC v7

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment (azacitidine)

Patients receive azacitidine subcutaneously on days 1-7. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Group Type: EXPERIMENTAL

Azacitidine

Intervention Type: DRUG

Given subcutaneously

Diagnostic Laboratory Biomarker Analysis

Intervention Type: OTHER

Correlative studies

Pharmacological Study

Intervention Type: OTHER

Correlative studies

Interventions

Azacitidine

Given subcutaneously

Intervention Type: DRUG

Diagnostic Laboratory Biomarker Analysis

Correlative studies

Intervention Type: OTHER

Pharmacological Study

Correlative studies

Intervention Type: OTHER

Other Intervention Names

5 AZC; 5-AC; 5-Azacytidine; 5-AZC; Azacytidine; Azacytidine, 5-; Ladakamycin; Mylosar; U-18496; Vidaza

Eligibility Criteria

Inclusion Criteria

• Advanced (stage 4 or recurrent) NSCLC, not eligible for any curative intent treatment

• Tumor must be histologically or cytologically confirmed
• Measurable disease (as defined by RECIST criteria)
• Patients may have up to two (and at least one) prior cytotoxic regimens in the metastatic setting

• Prior adjuvant chemotherapy following resection or definitive chemo-radiation for patients with locally advanced disease is not included in this
• Allowable systemic therapy in the metastatic setting includes 2 cytotoxic regimens and erlotinib and/or other non-cytotoxic drugs (i.e., erlotinib, sorafenib, and other tyrosine kinase inhibitors do not count as a "cytotoxic regimen")
• Prior adjuvant therapy or definitive chemo-radiation is allowed if completed > six months before the onset of "first-line" therapy in the metastatic setting - in this setting, adjuvant or definitive chemo-radiation will not "count" as one of the two cytotoxic regimens; if however, the patient relapses within six months from completion of adjuvant or definitive chemoradiation, then this therapy will be considered the first-line cytotoxic therapy
• In the unusual circumstance where patients receive "adjuvant" therapy following resection of oligo-metastatic disease (for example brain metastasis and lung primary resections) and the treating physician decides to administer chemotherapy following all surgery, this will be considered "adjuvant" therapy and the same rules as noted above will apply for initiation of first-line systemic therapy
• No patients with uncontrolled brain metastases or leptomeningeal disease

• Patients with controlled brain metastases are allowed
• ECOG performance status 0-2
• Absolute neutrophil count ≥ 1.5 x 10^9/L
• Platelets ≥ 100,000 x 10^9/L
• Hemoglobin ≥ 9.0 gm/100 mL
• Total bilirubin ≤ 1.5 mg/dL
• AST and ALT ≤ 2.5 x ULN
• Creatinine ≤ 1.5 mg/dL OR calculated creatinine clearance > 50 mL/min
• No patients who are pregnant
• Women of childbearing potential must have a negative pregnancy test
• The patient must be willing to use adequate contraception for the duration of study treatment and up to four weeks following the last dose of drug
• Archival diagnostic material sufficient for microRNA evaluation/assessment is preferred, though optional

• The presence of archival material will not preclude the need for pre and post treatment biopsies
• Willing to undergo biopsy pre-treatment and following first cycle

• Biopsy may be from any accessible site (primary or metastatic)
• No known HIV or hepatitis B or C (though testing for this is not required)
• No uncontrolled intercurrent illness including, but not limited to:

• Symptomatic CHF
• Unstable angina pectoris
• Serious cardiac arrhythmia
• Serious infection
• Psychiatric illness or social situations that would limit compliance with study requirements
• No patients who have significant psychiatric illness that, in the opinion of the principal investigator, would prevent adequate informed consent or render therapy unsafe
• Patients may not have had a prior invasive malignancy except for adequately treated non-melanoma cell skin cancer, in situ cervical cancer, or other cancer for which the patient has been disease-free for 2 years

• For example, a stage 1 (T1c) prostate cancer 2 years prior to a diagnosis of NSCLC would not be exclusionary, however, a metastatic prostate cancer currently receiving hormonal or chemotherapy would be excluded
• No other concurrent palliative radiotherapy
• Recovered from prior surgery, radiation, or chemotherapy to ≤ grade 2 toxicity
• Palliative radiation or surgical procedures (for example, endobronchial therapy) is allowed, but must have been completed > 2 weeks prior to starting treatment
• No other investigational or commercial agents or therapies may be administered with the intent to treat the patient's malignancy
• No other concurrent investigational therapy

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Gregory A Otterson

Role: PRINCIPAL_INVESTIGATOR

Ohio State University Comprehensive Cancer Center

Locations

Ohio State University Comprehensive Cancer Center

Columbus, Ohio, United States

Countries

United States

Other Identifiers

NCI-2011-02570

Identifier Type: REGISTRY

Identifier Source: secondary_id

CDR0000692184

Identifier Type: -

Identifier Source: secondary_id

OSU-10100

Identifier Type: -

Identifier Source: secondary_id

OSU 10100

Identifier Type: OTHER

Identifier Source: secondary_id

8617

Identifier Type: OTHER

Identifier Source: secondary_id

N01CM00070

Identifier Type: NIH

Identifier Source: secondary_id

View Link

P30CA016058

Identifier Type: NIH

Identifier Source: secondary_id

View Link

NCI-2011-02570

Identifier Type: -

Identifier Source: org_study_id