High-Dose Therapy Treatment in Patients With Follicular Lymphoma
Follicular Lymphoma
About this trial
This is an interventional treatment trial for Follicular Lymphoma focused on measuring Phase III study patients with follicular lymphoma
Eligibility Criteria
Inclusion Criteria:
- Age 18-60 years old
- Follicular Lymphoma B, C or D (Working Formulation)
- No previous treatment
- Seronegativity HIV
- ECOG performance status less than or 2
- eligible for autologous stem-cell transplantation
- Stage II , III or IV Ann Arbor Classification
- criterias of high tumor burden
- Patient's written informed consent
Exclusion Criteria:
- Age less than 18 years old or more than 60 years old
- Other type of lymphoma
- Stage less than 3 or III-IV (faible masse)
- Seropositivity HIV
- Patients with a history of another malignancy except basal cell skin cancer or in situ uterus cancer
Sites / Locations
- Emmanuel GYAN
- Philippe COLOMBAT
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
1
2
standard chemotherapy arm, the CHVP (cyclophosphamide, low-dose doxorubicin, teniposide, and prednisone) regimen consisted of cyclophosphamide (600 mg/m2), doxorubicin (25 mg/m2), and teniposide (60 mg/m2), all administered intravenously on day 1, and prednisone (40 mg/m2), administered orally on days 1 to 5.4,12 Treatment consisted of a 6-course induction phase administered monthly, followed, for responders and patients presenting a stable disease, by a maintenance phase that consisted of 1 cycle every 2 months for 1 year. Concomitant subcutaneous interferon alfa-2b was administered at 5 x 106 3 times a week for 18 months.
VCAP (cyclophosphamide, high-dose doxorubicin, prednisone, and vincristine) regimen as a first-line therapy combining vindesine (3 mg/m2) on day 1, cyclophosphamide (1500 mg/m2) on day 2, doxorubicin (80 mg/m2) on day 2, and prednisolone (50 mg/m2) on days 1 to 5, every 3 weeks.19,31,32 Patients in CR, VGPR, or PR after the second or third VCAP cycle continued on to stem-cell harvesting and received, before transplantation, one course of IMVP16 (ifosfamide, methotrexate, and VP-16), which combined ifosfamide (1.5 g/m2) and VP16 (100 mg/m2) on days 1 through 3, and methotrexate (30 mg/m2) on days 1 and 10. Patients with less than PR after the VCAP cycles received, as salvage therapy, 2 to 3 courses of DHAP (dexamethasone, high-dose cytarabine, and cisplatin) combining cisplatine (100 mg/m2) on day 1, cytarabine (4 g/m2) on day 2, and dexamethasone (40 mg/m2) on days 1 through 4. If at least a PR was obtained after DHAP, stem cells were harvested or patients were considered as failures