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 transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more cancer cells. PURPOSE: Randomized phase III trial to compare the effectiveness of two regimens of combination chemotherapy in treating patients who have intermediate-grade or immunoblastic lymphoma.

Condition	Treatment or Intervention	Phase
Lymphoma	Procedure: chemotherapy  Procedure: biological response modifier therapy  Procedure: radiation therapy  Procedure: interferon therapy  Procedure: colony-stimulating factor therapy  Procedure: peripheral blood stem cell transplantation  Procedure: cytokine therapy  Drug: bone marrow ablation with stem cell support  Drug: bleomycin  Drug: carmustine  Drug: cisplatin  Drug: cyclophosphamide  Drug: cytarabine  Drug: etoposide  Drug: filgrastim  Drug: idarubicin  Drug: ifosfamide  Drug: interferon alfa  Drug: leucovorin calcium  Drug: melphalan  Drug: methotrexate  Drug: methylprednisolone  Drug: mitoxantrone  Drug: vincristine	Phase III

Further Study Details: 

OBJECTIVES: I. Compare the efficacy of early intensification vs alternating triple chemotherapy in patients with intermediate-grade or immunoblastic lymphoma with poor prognostic features. II. Compare, in a prospective manner, the cost/benefit ratio of these regimens in these patients. III. Determine the value of monitoring minimal residual disease detection via in vitro culture methods and polymerase chain reaction analysis of peripheral stem cell apheresis products and by longitudinal monitoring of blood and bone marrow samples in these patients treated with these regimens.

PROTOCOL OUTLINE: This is a randomized study. Patients are stratified according to tumor score (3 or 4 vs 5 or 6). During the first course of induction, patients receive IDSHAP comprising idarubicin (IDA) and cisplatin IV continuously on days 1-4, cytarabine (ARA-C) IV over 2 hours on day 5, and methylprednisolone (MePRDL) IV over 15 minutes on days 1-5. During the second course of induction, patients receive MBIDCOS comprising vincristine, bleomycin, and cyclophosphamide IV over 15 minutes on day 1, IDA IV continuously and MePRDL IV over 15 minutes on days 1-3, methotrexate (MTX) IV over 2 hours on day 10, and oral leucovorin calcium every 6 hours on days 11 and 12. Each course lasts 3 weeks in the absence of disease progression or unacceptable toxicity. Patients with stable or responding disease after induction are randomized to 1 of 2 treatment arms. Arm I: Patients receive the following 3 courses of early intensification. First course: Patients receive ifosfamide (IFF) IV continuously and etoposide (VP-16) IV over 2 hours every 12 hours on days 1-3. Filgrastim (G-CSF) is administered subcutaneously (SC) beginning on day 5 and continuing until blood counts recover and then autologous peripheral blood stem cells (PBSC) are harvested, selected for CD34 positive cells, and purged in vitro. If more than 5% of the WBC contains lymphoma cells after induction, then 2 courses of IFF and VP-16 are administered before PBSC harvest. Second course: Patients receive IFF IV continuously on days 1-3, mitoxantrone (DHAD) IV on day 1, and G-CSF SC as in the first course. Third course: Patients receive carmustine IV over 1 hour on day -6, ARA-C and VP-16 IV every 12 hours on days -5 to -2, and melphalan IV on day -1. PBSC are reinfused on day 0. G-CSF is administered SC beginning on day 0 and continuing until blood counts recover. Each course lasts 3 weeks in the absence of disease progression or unacceptable toxicity. Arm II: Patients receive IDSHAP during courses 2 and 5, MBIDCOS during courses 3 and 6, and IFF and VP-16 IV over 1 hour on days 1-3 and DHAD IV over 15 minutes on day 1 during courses 1, 4, and 7. Each course lasts 4 weeks in the absence of disease progression or unacceptable toxicity. Patients with residual disease after completion of arm I or II treatment undergo radiotherapy to areas of bulk disease if feasible. Patients on both arms with meningeal involvement receive ARA-C intrathecally (IT) alternated with MTX every other day until 1 week after clearing of CNS disease and then 2 IT injections during every course of chemotherapy thereafter. Patients with divergent histology who achieve complete response after completion of arm I or II treatment receive interferon alfa 3 times a week for 1 year. Patients are followed at 1 month, every 3 months for 1 year, every 6 months for 1 year, and then annually for 2 years.

PROJECTED ACCRUAL: A maximum of 136 patients will be accrued for this study within 4 years.

Ages Eligible for Study:  15 Years   -   59 Years

Criteria

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

Diagnosis of previously untreated intermediate-grade or immunoblastic lymphoma

• Tumor score of 3 or greater, defined by the presence of 3 or more of the following criteria: *Ann Arbor stage III or IV disease *B symptoms (fever, sweats, and weight loss greater than 10%) *At least 1 tumor mass greater than 7 cm or mediastinal mass visible on plain chest x-ray *Beta-2 microglobulin at least 3.0 *Lactic dehydrogenase at least 1.1 times the upper limit of normal
• T- and B-cell lymphomas allowed if intermediate grade or immunoblastic
• Divergent histologies, including bone marrow involvement, allowed
• CNS involvement allowed

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.

--Prior/Concurrent Therapy--

No prior therapy

--Patient Characteristics--

Age: 15 to 59

Performance status: Not specified

Life expectancy: Not specified

Hematopoietic: Not specified

Hepatic: Bilirubin less than 2.0 mg/dL (unless elevation due to lymphoma)

Renal: Creatinine no greater than 1.5 mg/dL (unless elevation due to lymphoma)

Cardiovascular:

• LVEF greater than 50% by echocardiogram if over age 45
• No congestive heart failure, angina, history of myocardial infarction, or arrhythmia unless cleared by principal investigator after cardiology consultation

Pulmonary:

• No history of chronic obstructive or restrictive lung disease
• Pulmonary consultation required for smokers or patients with questionable lung function

Other:

• HIV negative
• Not pregnant or nursing
• Fertile patients must use effective contraception
• No prior malignancy with poor prognosis (less than 90% probability of surviving for 5 years)
• No geographic, economic, emotional, or social condition that would preclude study

Texas
      University of Texas - MD Anderson Cancer Center, Houston,  Texas,  77030-4009,  United States

Study chairs or principal investigators

Richard E. Champlin,  Study Chair,  M.D. Anderson Cancer Center   

Study ID Numbers:  CDR0000065044; MDA-DM-95121; NCI-V96-1010
Record last reviewed:  April 2003
Last Updated:  October 13, 2004
Record first received:  November 1, 1999
ClinicalTrials.gov Identifier:  NCT00002835
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08