Protocol for a Randomized Phase III Study of the Stanford V Regimen, Compared With ABVD for the Treatment of Advanced Hodgkin's Disease
OBJECTIVES:
- Compare relapse-free and overall survival of patients with previously untreated
advanced Hodgkin's lymphoma treated with bleomycin, doxorubicin, etoposide,
mechlorethamine, vinblastine, vincristine, and prednisone (Stanford V) vs doxorubicin,
bleomycin, vinblastine, and dacarbazine (ABVD).
- Compare the toxicity of these regimens in these patients.
OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2
treatment arms.
- Arm I (Stanford V): Patients receive mechlorethamine on weeks 1, 5, and 9; vinblastine
and doxorubicin on weeks 1, 3, 5, 7, 9, and 11; etoposide IV over 30-45 minutes for 2
consecutive days on weeks 3, 7, and 11; and vincristine and bleomycin on weeks 2, 4, 6,
8, 10, and 12. Patients also receive oral prednisone every other day on days 1-63
followed by a taper on days 64-84. Treatment continues for 12 weeks.
- Arm II (ABVD): Patients receive doxorubicin, bleomycin, vinblastine, and dacarbazine on
days 1 and 15. Treatment repeats every 28 days for 6-8 courses.
All patients achieving a complete remission or partial remission after chemotherapy undergo
involved field radiotherapy if they had initial bulky mediastinal disease, initial nodal
masses at least 5 cm in diameter, or initial splenic disease.
Patients are followed every 3 months for 1 year, every 4 months for 1 year, every 6 months
for 3 years, and then annually thereafter.
Peer Reviewed and Funded or Endorsed by Cancer Research UK
PROJECTED ACCRUAL: Approximately 700-850 patients will be accrued for this study.
Interventional
Allocation: Randomized, Primary Purpose: Treatment
Relapse-free survival
No
Peter J. Hoskin, MD
Study Chair
Mount Vernon Cancer Centre at Mount Vernon Hospital
United States: Federal Government
CDR0000069453
NCT00041210
October 2001
Name | Location |
---|