Combination Chemotherapy in Treating Patients With Newly Diagnosed Mantle Cell Lymphoma
Status: | Completed |
---|---|
Conditions: | Lymphoma |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 16 - Any |
Updated: | 11/16/2018 |
Start Date: | May 20, 1998 |
End Date: | April 18, 2007 |
Phase II CCOP Trial of High Dose Methotrexate/ARA-C and HCVAD for Newly Diagnosed Nodular and Diffuse Mantle Cell Lymphoma and Their Blastic Variants
RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing
so they stop growing or die. Combining more than one drug may kill more cancer cells.
PURPOSE: Phase II trial to study the effectiveness of different regimens of combination
chemotherapy in treating patients with newly diagnosed mantle cell lymphoma.
so they stop growing or die. Combining more than one drug may kill more cancer cells.
PURPOSE: Phase II trial to study the effectiveness of different regimens of combination
chemotherapy in treating patients with newly diagnosed mantle cell lymphoma.
OBJECTIVES:
- Evaluate the complete response rate and duration of response in patients with newly
diagnosed diffuse or nodular mantle cell lymphoma or their blastic variant treated with
high-dose methotrexate and cytarabine and high-dose cyclophosphamide, dexamethasone,
doxorubicin, and vincristine (HCVAD).
OUTLINE: This is a multicenter study. Patients may receive either regimen A or both regimen A
and regimen B, depending upon response.
- Regimen A: Patients receive methotrexate IV over 24 hours on day 1. Cytarabine is
administered IV over 2 hours every 12 hours on days 2 and 3. Filgrastim (G-CSF) is
administered subcutaneously (SC) daily beginning on day 4 and continuing until blood
counts recover. Treatment repeats every 21 days for up to 8 courses.
- Regimen B: Patients receive cyclophosphamide IV over 3 hours every 12 hours on days 1-3.
Doxorubicin is administered IV over 24 hours on days 4 and 5. Vincristine is
administered IV over 30 minutes on days 4 and 11. Dexamethasone is administered orally
or IV on days 1-4 and 11-14. G-CSF is administered SC beginning on day 6 and continuing
until blood counts recover. Treatment repeats every 21 days for up to 7 courses.
Patients are followed every 3 months for 1 year, every 4 months for 1 year, every 6 months
for 2 years, and then annually thereafter.
PROJECTED ACCRUAL: A total of 21-45 patients will be accrued for this study within 4 years.
- Evaluate the complete response rate and duration of response in patients with newly
diagnosed diffuse or nodular mantle cell lymphoma or their blastic variant treated with
high-dose methotrexate and cytarabine and high-dose cyclophosphamide, dexamethasone,
doxorubicin, and vincristine (HCVAD).
OUTLINE: This is a multicenter study. Patients may receive either regimen A or both regimen A
and regimen B, depending upon response.
- Regimen A: Patients receive methotrexate IV over 24 hours on day 1. Cytarabine is
administered IV over 2 hours every 12 hours on days 2 and 3. Filgrastim (G-CSF) is
administered subcutaneously (SC) daily beginning on day 4 and continuing until blood
counts recover. Treatment repeats every 21 days for up to 8 courses.
- Regimen B: Patients receive cyclophosphamide IV over 3 hours every 12 hours on days 1-3.
Doxorubicin is administered IV over 24 hours on days 4 and 5. Vincristine is
administered IV over 30 minutes on days 4 and 11. Dexamethasone is administered orally
or IV on days 1-4 and 11-14. G-CSF is administered SC beginning on day 6 and continuing
until blood counts recover. Treatment repeats every 21 days for up to 7 courses.
Patients are followed every 3 months for 1 year, every 4 months for 1 year, every 6 months
for 2 years, and then annually thereafter.
PROJECTED ACCRUAL: A total of 21-45 patients will be accrued for this study within 4 years.
DISEASE CHARACTERISTICS:
- Histologically confirmed previously untreated nodular or diffuse mantle cell lymphoma
or their blastic variant
- No CNS involvement
- Not a candidate for stem cell transplantation or refuses one
PATIENT CHARACTERISTICS:
Age:
- 16 and over
Performance status:
- Zubrod 0-2
Life expectancy:
- Not specified
Hematopoietic:
- Absolute neutrophil count greater than 1,000/mm^3*
- Platelet count greater than 100,000/mm^3* NOTE: * Unless lymphoma involvement
Hepatic:
- Bilirubin less than 1.5 mg/dL (unless lymphoma involvement)
Renal:
- Creatinine less than 2.0 mg/dL (unless lymphoma involvement)
Cardiovascular:
- Cardiac ejection fraction at least 50% (for patients over age 40)
Other:
- Must be willing to receive blood transfusion
- Not pregnant or nursing
- Fertile patients must use effective contraception
- HIV negative
- No other co-morbid medical or psychiatric illness that would preclude treatment
- No prior or concurrent malignancy with poor prognosis (less than 90% probability of
survival at 5 years)
PRIOR CONCURRENT THERAPY:
Biologic therapy
- See Disease Characteristics
Chemotherapy
- Not specified
Endocrine therapy
- Not specified
Radiotherapy
- Not specified
Surgery
- Not specified
We found this trial at
1
site
1515 Holcombe Blvd
Houston, Texas 77030
Houston, Texas 77030
713-792-2121
University of Texas M.D. Anderson Cancer Center The mission of The University of Texas MD...
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