Overview

Amifostine and High-Dose Combination Chemotherapy in Treating Patients With Acute Myeloid Leukemia or Chronic Myelogenous Leukemia

Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Chemoprotective drugs, such as amifostine, may protect normal cells from the side effects of chemotherapy. PURPOSE: Phase II trial to study the effectiveness of amifostine and high-dose combination chemotherapy in treating patients with acute myeloid leukemia or chronic myelogenous leukemia.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Rush University Medical Center
Collaborator:
National Cancer Institute (NCI)
Treatments:
Amifostine
Cytarabine
Mitoxantrone
Criteria
DISEASE CHARACTERISTICS: Newly diagnosed high risk acute myeloid leukemia (AML) defined as:
AML after myelodysplastic syndrome; refractory anemia with excess blasts in transformation
or "AML in evolution" also eligible AML following a chronic myeloproliferative disorder
(except chronic myelogenous leukemia) Therapy related AML or AML following exposure to a
known hematopoietic toxin Relapsed AML Age 70 or older OR AML in first relapse defined as:
AML in first relapse without treatment on protocol AML-9801 Relapsed following standard
chemotherapy Previously treated on AML-9701 and relapsed after at least 6 months of
remission OR Chronic myelogenous leukemia (CML) in blast crisis defined as: 20% or more
blast cells in the bone marrow or peripheral blood Pure lymphoid blastic crisis eligible if
resistant to an acute lymphocytic leukemia type treatment regimen or relapsed after initial
response to such a treatment

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: Karnofsky 60-100% Life
expectancy: Not specified Hematopoietic: Not specified Hepatic: Bilirubin less than 3 mg/dL
SGOT/SGPT no greater than 2.5 times upper limit of normal Renal: Creatinine less than 3
mg/dL Cardiovascular: No overt congestive heart failure or uncontrollable ventricular
arrhythmias No uncontrollable hypertension Neurologic: No cerebellar dysfunction Other: Not
pregnant or nursing Negative pregnancy test Fertile patients must use effective
contraception

PRIOR CONCURRENT THERAPY: See Disease Characteristics