Myelodysplastic Syndrome Clinical Trial

Lenalidomide Safety/Efficacy in Myelodysplastic Syndromes (MDS) Associated With a Deletion (Del)(5q) Cytogenetic Abnormality

Summary

This study is a multicenter, single-arm, open-label study of oral lenalidomide monotherapy administered to red blood cell (RBC) transfusion-dependent subjects with low- or intermediate-1-risk Myelodysplastic Syndromes (MDS) associated with a del (5q31-33) cytogenetic abnormality. Screening procedures will take place within 28 days of the first day of lenalidomide treatment. Subjects will receive lenalidomide in 28-day cycles for up to 6 cycles, or until bone marrow disease progression or progression/relapse following erythroid hematologic improvement is documented. Study visits will occur every cycle (every 28 days) and laboratory monitoring to assess hematological parameters will occur every 14 days. Safety and efficacy assessments to be performed during the study are outlined in the Schedule of Study Assessments.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Must understand and voluntarily sign an informed consent form
Age 18 years or older at the time of signing the informed consent
Must be able to adhere to the study visit schedule and other protocol requirements.
Diagnosis of low or intermediate-1-risk International Prognostic Scoring System (IPSS) Myelodysplastic Syndromes (MDS) without an abnormality of chromosome 5 involving a deletion between bands q31 and q33.
Red blood cell (RBC) transfusion-dependent anemia defined as having received greater than or equal to 2 units of RBCs within 8 weeks of the first day of study drug treatment.
Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1 or 2.
Women of childbearing potential (WCBP) must have a negative serum or urine pregnancy test within 7 days of starting study drug.
Sexually active WCBP must agree to use adequate contraceptive methods (oral, injectable, or implantable hormonal contraceptive; tubal ligation; intra-uterine device; barrier contraceptive with spermicide; or vasectomized partner) while on study drug.
WCBP must agree to have pregnancy tests every 4 weeks while on study drug.

Exclusion Criteria:

Pregnant or lactating females
Prior therapy with lenalidomide.
An abnormality of chromosome 5 involving a deletion between bands q31 and q33.
Lab Abnormality: Absolute neutrophil count (ANC) <500 cellmm^3 (0.5*10^9L)
Lab Abnormality: Platelet count <50,000/mm^3 (50*10^9/L)
Lab Abnormality: Serum creatinine >2.5 mg/dL (221 mmol/L)
Lab Abnormality: Serum total bilirubin >2.0 mg/dL (34 mmol/L)
Prior greater than or equal to grade 3 National Cancer Institute (NCI) Common Toxicity Criteria (CTC) allergic reaction/hypersensitivity to thalidomide.
Clinically significant anemia due to factors such as iron, B12 or folate deficiencies, autoimmune or hereditary hemolysis or gastrointestinal bleeding
If a marrow aspirate is not evaluable for storage iron, transferrin saturation must be > 20% and serum ferritin not less than 50 ng/mL
Use of hematopoietic growth factors within 7 days of the first day of study drug treatment.
Prior greater than or equal to grade 3 NCI CTC rash or any desquamation (blistering) while taking thalidomide.
Chronic use (>2 weeks) of greater than physiologic doses of a corticosteroid agent (dose equivalent to >10 mg/day of prednisone) within 28 days of the first day of study drug treatment.
Use of experimental or standard drugs (i.e. chemotherapeutic, immunosuppressive, and cytoprotective agents) for the treatment of MDS within 28 days of the first day of study drug treatment.
Prior history of malignancy other than MDS (except basal cell or squamous cell carcinoma or carcinoma in situ of the cervix or breast) unless the subject has been free of disease for greater than or equal to 3 years.
Use of any other experimental therapy within 28 days of the first day of study drug treatment.

Study is for people with:

Myelodysplastic Syndrome

Phase:

Phase 2

Estimated Enrollment:

148

Study ID:

NCT00065156

Recruitment Status:

Completed

Sponsor:

Celgene

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There are 30 Locations for this study

See Locations Near You

Arizona Cancer Center
Scottsdale Arizona, 85258, United States
Mayo Clinic
Scottsdale Arizona, 85259, United States
Arizona Cancer Center
Tucson Arizona, 85724, United States
Desert Hematology & Oncology Medical Group
Rancho Mirage California, 92270, United States
Stanford University Medical Center
Stanford California, 94305, United States
Mayo Clinic
Jacksonville Florida, 32224, United States
Cancer & Blood Disease Center
Lecanto Florida, 34461, United States
University of Miami Sylvester Comp Cancer Center
Miami Florida, 33136, United States
H. Lee Moffitt Cancer Center and Research Institute
Tampa Florida, 33612, United States
Northwest Georgia Oncology - Wellstar Cancer Research
Marietta Georgia, 30060, United States
Rush-Presbyterian- St. Luke's Medical Center
Chicago Illinois, 60612, United States
University of Chicago Medical Center
Chicago Illinois, 60637, United States
Midwest Cancer Research Group
Skokie Illinois, 60077, United States
Johns Hopkins Oncology Center
Baltimore Maryland, 21287, United States
Dana-Farber Cancer Institute
Boston Massachusetts, 02115, United States
Wayne State University School of Medicine
Detroit Michigan, 48201, United States
Mayo Clinic
Rochester Minnesota, 55905, United States
University of Nebraska Medical Center
Omaha Nebraska, 68198, United States
Roswell Park Cancer Institute
Buffalo New York, 14263, United States
New York Hospital-Cornell
New York New York, 10021, United States
Memorial Sloan-Kettering Cancer Center
New York New York, 10021, United States
Mt. Sinai Medical Center
New York New York, 10029, United States
University of Rochester- James P. Wilmot Cancer Center
Rochester New York, 14642, United States
Wake Forest University School of Medicine
Winston-Salem North Carolina, 27157, United States
The Cleveland Clinic Foundation
Cleveland Ohio, 44195, United States
Oregon Health & Science University
Portland Oregon, 97201, United States
Kaiser Permanente Northwest Region
Portland Oregon, 97227, United States
Western Pennsylvania Cancer Institute
Pittsburgh Pennsylvania, 15224, United States
MD Anderson Cancer Center
Houston Texas, 77030, United States
Swedish Cancer Institute
Seattle Washington, 98104, United States
Fred Hutchinson Cancer Research Center
Seattle Washington, 98109, United States
St. Johannes Hospital
Duisburg , , Germany

How clear is this clinincal trial information?

Study is for people with:

Myelodysplastic Syndrome

Phase:

Phase 2

Estimated Enrollment:

148

Study ID:

NCT00065156

Recruitment Status:

Completed

Sponsor:


Celgene

How clear is this clinincal trial information?

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