Last updated on September 2006
A Dose Study of Doxil in a Dose Dense 14 Day CDOP/Rituximab Regimen for Patients With Diffuse Large B-Cell Non-Hodgkin Lymphoma (NHL)> 60 Years or With Compromised Cardiac Status.
Are you eligible to participate in this study?
You may be eligible for this study if you meet the following criteria:
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Conditions: Diffuse Large B Cell Lymphoma | Lymphoma | Non-Hodgkin
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Age: Between 18 - 100 Years
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Gender: Male or Female
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Other:
60 years old and older or 18 years old and older with significant/potential cardiac morbidity Diagnosis of diffuse large B cell lymphoma, Ann Arbor stage I-IV, any International Prognostic Index (IPI) score. Previously untreated New York Heart Association (NYHA) classification of Class III or better Baseline ejection fraction (EF) > 25% Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-3 Unless attributable to NHL: absolute neutrophil count (ANC) > 1500/uL, platelets > 100,000/uL; hemoglobin > 9.0 g/dl Bilirubin < 1.5 mg/dL (unless related to lymphoma) Hepatic: transaminases < 2.5 x upper limit of normal (ULN) (unless related to lymphoma) Creatinine < 2.5 mg/dl (unless related to lymphoma)
You may not be eligible for this study if the following are true:
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No HIV+ individuals No primary central nervous system (CNS) lymphoma No pregnant or lactating women No serious active infection History of prior malignancy within the last 5 years other than subject's original cancer diagnosis listed in inclusion criteria with the exception of curatively treated basal cell carcinoma.