Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 10:34 AM
Ignite Modification Date:
2025-12-26 @ 10:34 AM
NCT ID:
NCT00848328
Eligibility Criteria:
DISEASE CHARACTERISTICS:
* Histologically\* confirmed non-Hodgkin lymphoma, including one of the following subtypes:
* Grade 1, 2, or 3a (\> 15 centroblasts per high-power field with centrocytes present) follicular lymphoma according to WHO criteria
* Small lymphocytic lymphoma
* NOTE: \*Bone marrow biopsies as the sole means of diagnosis are not acceptable, but they may be submitted in conjunction with nodal biopsies or extra-nodal biopsies; fine-needle aspirates are not acceptable for diagnosis.
* At least one measurable lesion according to RECIST criteria
* Measurable lymphadenopathy to follow with serial exam and/or imaging
* Relapsed or refractory disease
* Must have evidence of disease progression during or after last treatment
* If previously treated with rituximab, must have disease progression within 6 months of last therapy OR if there was a prior response to rituximab, rituximab must not have been given within the past 6 months
* No evidence of CNS metastases
PATIENT CHARACTERISTICS:
* ECOG performance status 0-2
* Life expectancy \> 3 months
* Absolute neutrophil count ≥ 1,000/mm³
* Platelet count ≥ 75,000/mm³
* Serum creatinine ≤ 2.0 mg/dL
* Total bilirubin ≤ 2.0 mg/dL
* Not pregnant or nursing
* Negative pregnancy test
* Fertile patients must use effective double method contraception for ≥ 28 days before, during, and for ≥ 28 days after completion of study therapy
* HIV negative
* Able to swallow lenalidomide
* Able to take aspirin (81 or 325 mg) daily or low molecular weight heparin as prophylactic anticoagulation
* No neuropathy ≥ grade 2
* No known active hepatitis A, B, or C
* No other malignancies within the past 5 years except treated basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix or breast
* No serious medical condition, laboratory abnormality, or psychiatric illness that would preclude the patient from signing the informed consent form
* No condition, including the presence of laboratory abnormalities, that would preclude study participation or confound the ability to interpret study data
* No known hypersensitivity to thalidomide or rituximab
* No development of erythema nodosum, if characterized by a desquamating rash while taking thalidomide or similar drugs
PRIOR CONCURRENT THERAPY:
* See Disease Characteristics
* At least 4 weeks since prior anticancer therapy, including radiotherapy, hormonal therapy, or surgery
* More than 28 days since prior experimental drug or therapy
* No prior lenalidomide
* No other concurrent anticancer agents or treatments, including radiotherapy or thalidomide
* No other concurrent investigational agents
* No concurrent sargramostim (GM-CSF)
* No other concurrent antilymphoma therapy, including steroids (except for the treatment of hypersensitivity reactions)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00848328
Study Brief:
Protocol Section:
NCT00848328