Filgrastim and Chemotherapy Followed by Peripheral Stem Cell Transplant in Treating Patients With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma

• Status: Completed
• Trial end date: 2007-02-01
• Target enrollment: 0
• Participant gender: All

Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining chemotherapy with peripheral stem cell transplant may allow the doctor to give higher doses of chemotherapy drugs and kill more cancer cells. Colony-stimulating factors such as filgrastim may increase the number of immune cells found in bone marrow or peripheral blood and may help a person's immune system recover from the side effects of chemotherapy.

PURPOSE: This phase II trial is studying how well giving filgrastim together with chemotherapy and peripheral stem cell transplant works in treating patients with Hodgkin's lymphoma or non-Hodgkin's lymphoma.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Masonic Cancer Center, University of Minnesota
• Treatments: Carmustine; Cyclophosphamide; Cytarabine; Dexamethasone; Etoposide; Lenograstim; Mitoxantrone

Criteria

DISEASE CHARACTERISTICS:

• One of the following histologically confirmed diagnoses

• High grade non-Hodgkin's lymphoma:

• Immunoblastic or small noncleaved cell lymphoma (Burkitt's or non-Burkitt's) in complete or partial remission after initial therapy

• Localized (stage I or Zeigler stage A) small noncleaved (Burkitt's or non-Burkitt's) after relapse or incomplete response to initial therapy

• Lymphoblastic lymphoma in second or greater complete or partial response

• High risk lymphoblastic lymphoma in first complete remission or after initial therapy (high risk factors include stage IV disease, LDH greater than 2 times normal, and 2 or more extranodal sites)

• Intermediate grade non-Hodgkin's lymphoma:

• Diffuse large cell lymphoma

• Diffuse mixed cell lymphoma

• Diffuse small cleaved cell lymphoma

• Follicular large cell lymphoma

• In second or greater complete or partial remission OR

• High risk in first complete remission or after initial therapy

• High risk features include:

• No complete response after 12 weeks of initial combination chemotherapy

• Bulky disease (greater than 10 cm nodal masses or mediastinal disease involving greater than 1/3 of the chest diameter

• Malignant pleural effusion

• Liver involvement

• LDH greater than 2 times upper limit of normal at diagnosis

• At least 2 extranodal sites

• Low grade non-Hodgkin's lymphoma:

• Follicular small cleaved cell lymphoma

• Follicular mixed cell lymphoma

• Diffuse small lymphocytic lymphoma

• In first or greater complete response OR

• Following initial treatment if complete response is not achieved

• In second or greater complete or partial response if treated at diagnosis without clinical symptoms necessitating treatment

• T-cell lymphoma (nonlymphoblastic, intermediate, or high grade lymphomas) after initial therapy whether or not complete response is achieved

• Hodgkin's lymphoma

• Stage I and II disease treated with primary radiotherapy and failure of at least one combination chemotherapy regimen

• Stage III and IV disease with failure on mechlorethamine, vincristine, procarbazine, and prednisone (MOPP)-like regimen, alternative noncross resistant regimen (e.g., doxorubicin, bleomycin, vinblastine, and dacarbazine [ABVD]), or a combination (e.g., MOPP-ABV)

• High risk features allowed including:

• Failure to achieve initial complete remission with MOPP and/or ABVD and crossover or hybrid therapy

• Relapse within 6 months after initial therapy

• Relapse after initial radiotherapy with complete response longer than 1 year since initial therapy and subsequent failure on MOPP and/or ABVD or hybrid

• Bulky mediastinal disease after initial therapy and residual mass of at least 5 cm with other features of persisting disease (e.g., Gallium scan positive, high LDH, enlarging on serial x-rays, or positive biopsy)

• No HIV or HTLV-1 associated lymphomas

• No resistant or refractory lymphoma (no partial response following up to 3 courses of combination chemotherapy)

• No active ischemic or degenerative CNS disease NOTE: A new classification scheme for adult non-Hodgkin's lymphoma has been adopted by PDQ. The terminology of "indolent" or "aggressive" lymphoma will replace the former terminology of "low", "intermediate", or "high" grade lymphoma. However, this protocol uses the former terminology.

PATIENT CHARACTERISTICS:

Age:

• 70 and under

Performance status:

• Age 65-70 years:

• Karnofsky 80-100%

• Under 65 years:

• ECOG 0-1 (2 allowed if symptoms are directly related to lymphoma)

Life expectancy:

• Greater than 8 weeks

Hematopoietic:

• Not specified

Hepatic:

• No prior or current chronic liver disease

• Bilirubin no greater than 1.5 mg/dL

• AST and alkaline phosphatase less than 2 times normal

Renal:

• Age 65-70 years:

• Creatinine clearance greater than 60 mL/min (if creatinine at least 1.5 mg/dL)

• Under 65 years:

• Creatinine no greater than 1.5 mg/dL OR

• Creatinine clearance greater than 50 mL/min

Cardiovascular:

• LVEF at least 45% by MUGA

• No symptoms of cardiac disease

• No active ischemic heart disease

• No uncontrolled hypertension

Pulmonary:

• Age 65-70 years:

• If history of smoking or respiratory symptoms, spirometry and DLCO must be greater than 50% of predicted

• All ages:

• No obstructive airway disease

• No resting hypoxemia (PO_2 less than 80)

• DLCO at least 50% of predicted

Other:

• No poorly controlled diabetes

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• Not specified

Chemotherapy:

• See Disease Characteristics

• Must have prior chemotherapy to attempt to achieve complete response

Endocrine therapy:

• Not specified

Radiotherapy:

• See Disease Characteristics

• No radiotherapy to residual disease prior to transplantation

Surgery:

• Not specified

Other:

• Concurrent IV antibiotic therapy allowed for fever or signs of infection