Basic Trial Information
Trial Description
     Summary
     Further Trial Information
     Eligibility Criteria
Trial Contact Information

Basic Trial Information

Trial Description

Summary

Background:

• Large granular lymphocyte (LGL) leukemia is a low-grade non-Hodgkin's lymphoma.

• LGL is associated with low numbers of white blood cells (leading to recurring infections), red blood cells (causing anemia) and platelets (causing abnormal bleeding).

• Cyclosporine (CSA) is an immunosuppressive drug that improves low blood cell counts in about 50 percent of patients with LGL leukemia.

Objectives:

• To identify what factors determine why cyclosporine works in some patients and not in others.

• To identify what causes low blood counts in LGL leukemia.

Eligibility: Patients 18 years of age and older with LGL leukemia.

Design:

• Patients have a medical history, physical examination blood tests, bone marrow biopsy and x-ray studies, including chest x-rays and CT scans of the chest, abdomen and pelvis. Patients with an easily accessible enlarged lymph node have a node biopsy (removal of a small piece of tissue for microscopic examination).

• Patients take cyclosporine twice a day by mouth. Blood samples are taken at least weekly to monitor drug levels.

• Patients undergo apheresis (collection of white blood cells) at a number of different time points in the study (maximum 6 times) to look at the differences in the leukemia cells before and during treatment with cyclosporine. For apheresis, blood is withdrawn through a needle in an arm vein and directed through a catheter (plastic tube) into a machine that separates it into its components. The white cells are extracted and the rest of the blood is returned through the same needle or through a second needle in the other arm.

Further Study Information

Background:

• LGL leukemia is a low grade non-Hodgkins Lymphoma characterized by tissue invasion of the marrow, spleen and liver

• Recurrent infections due to chronic neutropenia and transfusion-dependent anemia are the principal causes for initiation of therapy

• Approximately 50% of patients treated with cyclosporine (CSA) respond to treatment. CSA appears to correct the associated cytopenia without decreasing LGL numbers, suggesting it may inhibit LGL secretion of yet unidentified mediators of neutropenia and anemia.

• Analysis of differential gene expression profiles in patients with LGL leukemia treated with cyclosporine has the potential to detect as yet unidentified, therapeutic targets and possibly provide predictors of CSA responsiveness.

Objective:

• Identify changes in gene expression patterns induced by cyclosporine therapy in patients with LGL leukemia

• Identify differences between responding and non-responding patients

Eligibility:

-Patients with Large Granular Lymphocyte leukemia

Design:

• Patients will be treated with cyclosporine at a dose of 5-10mg/kg/day in divided doses, with doses adjusted to maintain a therapeutic serum level between 200-400ng/ml. These therapeutic levels shall be maintained for 3 months.

• Tumor response will be evaluated after 3 months therapy, the dose of CsA may then be tapered to that required to sustain a response or discontinued if no evidence of response, or after relapse.

• Blood sampling or Lymphapheresis for collection of circulating malignant cells will be performed at a number of different time points. Gene expression profiling will be carried out on Affymetrix microarrays to compare pretreatment and post-treatment samples.

Eligibility Criteria

• INCLUSION CRITERIA:

1. All patients must have a histologic or cytologic diagnosis of T-cell LGL leukemia as determined by the Laboratory of Pathology or Hematology at the Clinical Center, National Institutes of Health

2. All patients must have hemocytopenias such as granulocyte count less than 1,200/ul, platelet count less than 100,000/ul or hemoglobin less than 10 g/dl, or require hematopoietic support (transfusion or colony stimulating factors) to maintain counts at these or higher levels.

3. Patients must have measurable or evaluable disease

4. Patients must have a creatinine of less than 2.0 mg/dl.

5. Omission of cytotoxic chemotherapy for 3 weeks prior to entry into the trial is required. However, patients receiving stable corticosteroids will be eligible.

6. Age greater than 18 years

7. Karnofsky performance greater than 70%

8. Patients must have a life expectancy of greater than 3 months.

9. Patients must be able to understand and sign an Informed Consent form.

10. All female patients must use adequate contraception during participation in this trial and for three months after completing therapy.

EXCLUSION CRITERIA:

1. Patients with uncontrolled hypertension

2. Pregnant and nursing patients are not eligible for the study as CSA crosses the placenta. Based on clinical use, premature births and low birth weight were consistently observed. Breast-feeding is contraindicated because CSA enters the blood milk and may possibly be administered to the child.

3. Underlying immunodeficiency state including HIV seropositivity.

4. Positive for antibodies to hepatitis C or positive for hepatitis B surface antigen,

5. Patients with serious intercurrent illnesses, concurrent hepatic, renal, cardiac, neurologic, pulmonary, infectious or metabolic disease of such severity that it would preclude the patients' ability to tolerate cyclopsorine.

6. Patients who received cyclosporine for LGL leukemia previously and failed to respond.

Trial Contact Information

Trial Lead Organizations/Sponsors

National Cancer Institute

Link to the current ClinicalTrials.gov record.
NLM Identifer NCT00363779
Information obtained from ClinicalTrials.gov on December 14, 2011

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