Monoclonal Antibody Therapy and Combination Chemotherapy in Treating Patients With Stage II, Stage III, or Stage IV Diffuse Large B-Cell Lymphoma

You may be eligible if

• DISEASE CHARACTERISTICS:
• Histologically confirmed diffuse large B-cell lymphoma
• * B-cell phenotype (CD20+) as determined by immunohistochemistry (IHC) or flow cytometry
• * Stage II, III, or IV disease
• CD22+ tumor by IHC\*
• NOTE: \*CD22 status may be determined after study enrollment
• Measurable disease, defined as at least 1 lesion ≥ 1.5 cm by CT scan or physical exam
• No relapsed or refractory non-Hodgkin's lymphoma
• No history of transformed lymphoma
• No CNS lymphoma
• * CNS symptoms or bone marrow or sinus involvement must have absence of CNS lymphoma confirmed by lumbar puncture
• PATIENT CHARACTERISTICS:
• Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-3
• \- For patients with ECOG PS 3, the PS must be disease related
• Absolute neutrophil count ≥ 1,500/mm\^3
• Platelet count ≥ 100,000/mm\^3
• Total bilirubin ≤ 2 mg/dL (if total bilirubin \> 2 mg/dL, direct bilirubin should be within normal limits)
• AST ≤ 3 times upper limit of normal (ULN) (5 times ULN if there is liver involvement)
• Creatinine ≤ 2 times ULN
• Life expectancy ≥ 12 weeks
• Negative pregnancy test
• Not pregnant or nursing
• Fertile patients must use effective contraception during and for 12 months after completion of study treatment
• No active serious infection requiring antibiotics
• No New York Heart Association class III or IV heart disease
• No other primary malignancy within the past 5 years, except for squamous cell or basal cell carcinoma of the skin, in situ carcinoma of the cervix, or previously treated prostate cancer with a stable prostate-specific antigen
• No known HIV positivity
• No known hepatitis B or C infection
• Ejection fraction ≥ 45% by MUGA or echocardiogram (required if patients has a history of heart disease or is ≥ 50 years old)
• Willing to provide blood and tissue samples for mandatory translational research component of study
• PRIOR CONCURRENT THERAPY:
• No prior therapy for diffuse large B-cell lymphoma, including the following:
• * Chemotherapy
• * Immunotherapy
• * Biologic therapy
• * Radiotherapy
• Prior short course (≤ 14 days) of corticosteroids allowed
• Prior splenectomy allowed
• No prior pelvic irradiation
• No other concurrent investigational agents
• No concurrent chemotherapy, immunotherapy, or radiotherapy
• No concurrent enrollment on another treatment study involving a pharmacologic agent (e.g., drugs, biologics, immunotherapy, or gene therapy)