Lung Cancer Clinical Trial

Decitabine in Treating Patients With Unresectable Lung or Esophageal Cancer or Malignant Mesothelioma of the Pleura

Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.

PURPOSE: Phase I trial to study the effectiveness of decitabine in treating patients who have unresectable lung or esophageal cancer or malignant mesothelioma of the pleura.

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Full Description

OBJECTIVES:

Determine the pharmacokinetics, toxicity, and maximum tolerated dose of decitabine in patients with unresectable primary small cell or non-small cell lung cancer, unresectable esophageal cancer, or malignant pleural mesothelioma.
Measure the expression of NY-ESO-1 in tissue samples of these patients before and after receiving this drug.
Assess the serologic response to NY-ESO-1 in these patients before and after receiving this drug.
Measure the expression of p16 tumor suppressor gene in these patients before and after receiving this drug.

OUTLINE: This is a dose-escalation study for each stratification group. Patients are stratified according to number of prior therapies (2 or fewer vs 3 or more).

Patients receive decitabine IV continuously on days 1-3. Treatment repeats every 5 weeks for 2 courses in the absence of disease progression or unacceptable toxicity. Patients with stable or responding disease after completion of the second course receive 2 additional courses.

Cohorts of 3-6 patients receive escalating doses of decitabine until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 6 patients experience dose-limiting toxicity. Once the MTD is determined for a particular stratum, additional patients from that stratum are treated at the MTD.

Patients are followed for 1 month.

PROJECTED ACCRUAL: A maximum of 72 patients (36 per stratum) will be accrued for this study.

View Eligibility Criteria

Eligibility Criteria

DISEASE CHARACTERISTICS:

Histologically or cytologically confirmed unresectable primary small cell lung cancer (SCLC) or non-small cell lung cancer (NSCLC), unresectable esophageal cancer, malignant pleural mesothelioma, or pleural effusions secondary to extrathoracic malignancies
Disease must be readily accessible to biopsy by endoscopy or percutaneous fine-needle aspiration

Extrathoracic metastatic disease allowed if no evidence of active intracranial or leptomeningeal metastases

Patients treated with prior resection or radiotherapy for intracranial metastatic disease may be eligible provided there is no evidence of active disease on two MRIs (taken one month apart) and patients require no anticonvulsant medications or steroids to control residual symptoms
No limited stage SCLC or operable NSCLC

PATIENT CHARACTERISTICS:

Age:

18 and over

Performance status:

ECOG 0-2

Life expectancy:

At least 6 months

Hematopoietic:

Platelet count greater than 100,000/mm^3
Hemoglobin greater than 10 g/dL
WBC greater than 3,500/mm^3

Hepatic:

PT normal
Bilirubin less than 1.5 times upper limit of normal

Renal:

Creatinine no greater than 1.6 mg/dL OR
Creatinine clearance greater than 60 mL/min

Cardiovascular:

Any of the following conditions require clearance by a cardiologist:

Prior coronary artery disease
Prior transmural myocardial infarction
Congestive heart failure
Fixed defects on thallium scan with ejection fraction greater than 40%
No unstable angina
No recent deep venous thrombosis requiring anticoagulation

Pulmonary:

FEV1 and DLCO greater than 30% of predicted
pCO_2 less than 50 mm Hg
pO_2 greater than 60 mm Hg on room air
No recent pulmonary embolism requiring anticoagulation

Other:

Not pregnant or nursing
Negative pregnancy test
Fertile patients must use effective contraception
No active infection
HIV negative

PRIOR CONCURRENT THERAPY:

Biologic therapy:

At least 30 days since prior biologic therapy for the malignant tumor

Chemotherapy:

No prior decitabine
At least 30 days since other prior chemotherapy for the malignant tumor

Endocrine therapy:

See Disease Characteristics

Radiotherapy:

See Disease Characteristics
At least 30 days since prior radiotherapy for the malignant tumor (14 days for localized radiotherapy to nontarget lesions) and recovered

Surgery:

See Disease Characteristics

Study is for people with:

Lung Cancer

Phase:

Phase 1

Study ID:

NCT00019825

Recruitment Status:

Completed

Sponsor:

National Cancer Institute (NCI)

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There is 1 Location for this study

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Warren Grant Magnuson Clinical Center - NCI Clinical Studies Support
Bethesda Maryland, 20892, United States
Center for Cancer Research
Bethesda Maryland, 20892, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 1

Study ID:

NCT00019825

Recruitment Status:

Completed

Sponsor:


National Cancer Institute (NCI)

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