High-Dose Chemo-Radiotherapy for Patients With Primary Refractory and Relapsed Hodgkin's Disease
OBJECTIVES:
- Assess the efficacy of a high-dose chemoradiotherapy regimen in patients with
refractory or relapsed Hodgkin's lymphoma.
OUTLINE: Patients are stratified into 1 of 3 treatment arms (0-1 adverse prognostic factors
vs 2 adverse prognostic factors vs 3 adverse prognostic factors).
- Arm I (0-1 adverse prognostic factors): Patients receive ifosfamide by 24 hour infusion
on day 2. Carboplatin is administered on day 2. Etoposide IV is administered once daily
on days 1-3. Patients then receive filgrastim (G-CSF) subcutaneously or IV on days
5-12. Patients receive another course of ICE chemotherapy 2-3 weeks after the first
course.
Leukapheresis is performed once WBC reaches at least 3000/mm^3 and continues until enough
peripheral blood stem cells are collected.
Patients who have never received prior radiotherapy will receive accelerated
hyperfractionated total lymphoid irradiation (TLI) twice a day for 5 days (days -10 to -6).
Cyclophosphamide IV is then administered on days -5 and 4. Etoposide IV is administered by
continuous infusion over 4 days (days -5 to -2).
Patients who have had prior radiotherapy receive high dose chemotherapy. Cyclophosphamide IV
is administered on days -6 and -5. Etoposide IV is administered by continuous infusion over
4 days (days -6 to -3). Carmustine IV is administered on day -2.
Peripheral blood stem cells are infused 24-36 hours after high-dose chemotherapy. G-CSF is
administered beginning on day 1 and continuing until blood counts recover.
- Arm II (2 adverse prognostic factors): Patients receive the first course of ICE as in
Arm I.
Apheresis is performed once WBC is greater than 3000/mm^3 and continues until enough cells
are collected. The second course of ICE is then administered.
Ifosfamide is administered by 48 hour continuous infusion on days 1-2. Carboplatin is
administered on day 3. Etoposide IV is administered every 12 hours for 3 doses beginning on
day 1. Patients receive G-CSF on days 5-14.
Patients who have never received prior radiotherapy will receive accelerated
hyperfractionated TLI for 5 days (days -10 to -6). Cyclophosphamide IV is then administered
every 12 hours on days -5 to -2. Etoposide IV is administered by continuous infusion over 4
days (days -5 to -2).
Patients who have had prior radiotherapy receive high-dose chemotherapy. Cyclophosphamide IV
is administered every 12 hours on days -6 to -3. Etoposide IV is administered by continuous
infusion over 4 days (days -6 to -3). Carmustine IV is administered on day -2.
Peripheral blood stem cells are infused 24-36 hours after high dose chemotherapy. G-CSF is
administered beginning on day 1 and continuing until blood counts recover.
- Arm III (3 adverse prognostic factors): Patients receive cyclophosphamide IV daily for
2 days, then G-CSF beginning on day 4 until blood stem cells are collected.
Patients then undergo apheresis until enough cells are collected.
Patients receive high-dose chemotherapy. Ifosfamide IV is administered for 1 hour. Etoposide
is administered by continuous infusion for 12 hours. Carboplatin IV is administered for 1
hour. Etoposide is again administered by continuous infusion for 12 hours. Treatment is
repeated daily for 5 days.
Peripheral blood stem cells are reinfused 24-36 hours after the last dose of chemotherapy.
G-CSF is administered beginning on day 1 and continuing until blood counts recover.
Patients who have never received prior radiation will now receive accelerated
hyperfractionated TLI twice daily for 5 days. Patients receive a second course of high dose
chemotherapy 45-90 days after reinfusion of cells. Etoposide IV and cytarabine IV are
administered every 12 hours for 4 days (days -6 to -3). Melphalan IV is administered on day
-2.
Patients who have received prior radiation therapy receive a second course of high-dose
chemotherapy. Carmustine IV is administered on day -7. Etoposide IV and cytarabine IV are
administered every 12 hours for 4 days (days -6 to -3). Melphalan IV is administered on day
-2.
Peripheral blood stem cells are reinfused 24-48 hours after completion of second course
chemotherapy. G-CSF is administered beginning on day 1 and continuing until blood counts
recover.
Patients are followed every 3 months for the first 2 years, every 4 months during years 3-5,
and every 6 months thereafter.
PROJECTED ACCRUAL: This study will accrue 80 patients within 4 years.
Interventional
Primary Purpose: Treatment
Joachim Yahalom, MD
Study Chair
Memorial Sloan-Kettering Cancer Center
United States: Federal Government
CDR0000066714
NCT00003631
August 1998
Name | Location |
---|---|
Memorial Sloan-Kettering Cancer Center | New York, New York 10021 |