This trial is active, not recruiting.

Conditions recurrent non-small cell lung carcinoma, stage iv non-small cell lung cancer
Treatments azacitidine, diagnostic laboratory biomarker analysis, pharmacological study
Phase phase 2
Sponsor National Cancer Institute (NCI)
Start date January 2011
End date April 2011
Trial size 1 participant
Trial identifier NCT01281124, 8617, CDR0000692184, N01CM00070, NCI-2011-02570, OSU 10100, OSU-10100, P30CA016058


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.

United States No locations recruiting
Other countries No locations recruiting

Study Design

Intervention model single group assignment
Primary purpose treatment
Masking no masking
Patients receive azacitidine subcutaneously on days 1-7. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
azacitidine 5 AZC
Given subcutaneously
diagnostic laboratory biomarker analysis
Correlative studies
pharmacological study
Correlative studies

Primary Outcomes

DNA Hypomethylation and Re-expression of Silenced Tumor Suppressor Genes When Stratified for Low or High Expression of mir29
time frame: Up to 12 weeks after completion of study treatment

Secondary Outcomes

Overall Survival
time frame: From the day of initial treatment until death (from any cause), assessed up to 12 weeks after completion of study treatment
Progression-free Survival
time frame: From the day of initial treatment until documented disease progression (per PET) or death, assessed up to 12 weeks after completion of study treatment

Eligibility Criteria

All participants at least 18 years old.

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

Additional Information

Official title Pilot Phase II Study of 5-Azacytidine in Previously Treated Patients With Advanced NSCLC
Principal investigator Gregory Otterson
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.
Trial information was received from ClinicalTrials.gov and was last updated in March 2017.
Information provided to ClinicalTrials.gov by National Cancer Institute (NCI).