RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with peripheral stem cell transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more tumor 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: Phase II trial to study the effectiveness of filgrastim and chemotherapy followed by peripheral stem transplantation in treating patients who have Hodgkin's lymphoma or non-Hodgkin's lymphoma.

Condition	Treatment or Intervention	Phase
Hodgkin's lymphoma adult T-cell leukemia and lymphoma Non-Hodgkin's Lymphoma	Drug: carmustine  Drug: cyclophosphamide  Drug: cytarabine  Drug: dexamethasone  Drug: etoposide  Drug: filgrastim  Drug: mitoxantrone  Procedure: biological response modifier therapy  Procedure: bone marrow ablation with stem cell support  Procedure: chemotherapy  Procedure: colony-stimulating factor therapy  Procedure: cytokine therapy  Procedure: peripheral blood stem cell transplantation  Procedure: radiation therapy	Phase II

Further Study Details: 

OBJECTIVES:

• Assess the clinical outcomes, survival, and morbidity of transplantation in patients with Hodgkin's lymphoma or non-Hodgkin's lymphoma when treated with filgrastim (G-CSF) followed by high dose chemotherapy plus G-CSF followed by autologous peripheral blood stem cell (PBSC) transplantation.
• Determine whether sufficient PBSC can be collected for use in autologous transplantation in these patients when mobilized with hematopoietic growth factor alone compared to chemotherapy plus growth factor.
• Determine whether these primed PBSC support prompt lymphoid and myeloid hematopoietic recovery after transplantation in these patients.
• Compare the numbers of committed progenitor cells and/or primitive, pluripotential hematopoietic stem cells with these two priming techniques.
• Compare the numbers of tumor cells in cryopreserved PBSC following these priming techniques.
• Evaluate response and extended relapse free survival in conjunction with rapid hematopoietic reconstitution and limited transplant associated morbidity and mortality in these patients when treated with these regimens.

OUTLINE: In the first priming phase, patients receive filgrastim (G-CSF) subcutaneously (SQ) daily on days 1-7 and peripheral blood stem cells are collected on days 6-8.

At least 48 hours after the last dose of G-CSF and after the third leukapheresis, patients receive the second priming, which consists of cyclophosphamide IV over 2 hours on day 1 and cytarabine IV over 1 hour every 12 hours for a total of 2 doses on day 1. Patients also receive mitoxantrone IV over 1 hour daily and dexamethasone IV every 12 hours for a total of 4 doses on days 1-2. Patients receive G-CSF SQ daily beginning on day 4 and continuing until the completion of leukapheresis. PBSC are collected on 3 consecutive days after blood counts recover.

In the transplant phase, patients with non-Hodgkin's lymphoma who have not exceeded pretransplant radiotherapy limits receive cyclophosphamide IV over 2 hours on days -7 and -6 and total body irradiation twice daily on days -4 through -1. Autologous PBSC are reinfused on day 0. Patients receive G-CSF IV daily beginning on day 0 and continuing until day 21 or until blood counts recover.

Patients with Hodgkin's lymphoma or patients with non-Hodgkin's lymphoma who have exceeded pretransplant radiotherapy limits receive cyclophosphamide IV over 2 hours daily on days -6 through -3, carmustine IV over 1 hour on day -6, and etoposide IV over 4 hours every 12 hours for a total of 6 doses on days -6 through -4. Autologous PBSC are reinfused on day 0. Patients also receive G-CSF IV daily beginning on day 0 and continuing until day 21 or until blood counts recover.

All patients receive radiotherapy for any residual nodal masses measuring at least 2 cm 5 days a week beginning on day 28.

Patients are followed at day 100, then every 3 months for 1 year, then every 6 months for 2 years, and then annually thereafter.

PROJECTED ACCRUAL: A total of 30 patients will be accrued for this study over 18-24 months.

Ages Eligible for Study:  up to  70 Years,  Genders Eligible for Study:  Both

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

Minnesota
      University of Minnesota Cancer Center, Minneapolis,  Minnesota,  55455,  United States; Recruiting

Study chairs or principal investigators

Daniel J. Weisdorf, MD,  Study Chair,  University of Minnesota Cancer Center   

Study ID Numbers:  CDR0000067973; UMN-MT-9527; UMN-MT-1995-27; NCT00005985
Record last reviewed:  October 2000
Last Updated:  April 4, 2005
Record first received:  July 5, 2000
ClinicalTrials.gov Identifier:  NCT00005985
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08