RATIONALE: Amifostine may be effective in helping blood counts return to normal in treating patients with myelodysplastic syndrome. PURPOSE: Phase II trial to study the effectiveness of amifostine in treating patients with advanced myelodysplastic syndrome.
OBJECTIVES: I. Determine the overall hematologic response rate to amifostine in patients with advanced myelodysplastic syndrome. II. Determine the toxic effects of amifostine in these patients. OUTLINE: This is an open label study. Patients receive intravenous amifostine over 15 minutes three times a week. Patients failing to respond by 8 weeks undergo dose escalation. Nonresponding patients are removed from the study by 12 weeks. Therapy is continued for up to six months in responding patients. Patients are observed for duration of response upon therapy discontinuation. Patients who relapse will have therapy resumed at the previous dose. Patients will be followed until death. PROJECTED ACCRUAL: A maximum of 36 patients will be accrued.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
Enrollment
36
Osteopathic Medical Oncology and Hematology, P.C.
Clinton Township, Michigan, United States
Barbara Ann Karmanos Cancer Institute
Detroit, Michigan, United States
Henry Ford Hospital
Detroit, Michigan, United States
Garden City Hospital
Garden City, Michigan, United States
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Marquette General Hospital
Marquette, Michigan, United States
Providence Hospital Cancer Center
Southfield, Michigan, United States
Cleveland Clinic Cancer Center
Cleveland, Ohio, United States