Comparison of Liposomal Doxorubicin Used Alone or in Combination With Bleomycin Plus Vincristine in the Treatment of Kaposi's Sarcoma in Patients With AIDS
Sarcoma, Kaposi, HIV Infections
About this trial
This is an interventional treatment trial for Sarcoma, Kaposi focused on measuring Vincristine, Sarcoma, Kaposi, Liposomes, Doxorubicin, Drug Therapy, Combination, Granulocyte Colony-Stimulating Factor, Acquired Immunodeficiency Syndrome, Bleomycin, Drug Carriers
Eligibility Criteria
Inclusion Criteria Concurrent Medication: Allowed: G-CSF. Licensed or Treatment IND-approved antiretrovirals ( AZT, ddI, ddC, d4T ). PCP prophylaxis (required if CD4 count < 200 cells/mm3). Chemoprophylaxis or maintenance for bacterial infections, candidiasis, MAC, and herpes simplex. Up to 14 days of metronidazole. Recombinant erythropoietin. Patients must have: Documented HIV infection. Advanced stage Kaposi's sarcoma. No active acute opportunistic infection. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: Significant pulmonary insufficiency (unless due to pulmonary KS). Significant cardiac insufficiency. Other active malignancies except for basal or squamous cell carcinoma of the skin or in situ cervical cancer. Grade 2 or worse peripheral neuropathy. Altered mental status that prevents informed consent. Active Mycobacterium tuberculosis. Hypersensitivity or allergic reaction to any study drugs or E. coli-derived medications such as filgrastim (G-CSF). Concurrent Medication: Excluded: GM-CSF. Drugs associated with peripheral neuropathy (other than approved antiretrovirals and vincristine). Multi-drug therapy for active Mycobacterium tuberculosis (although isoniazid and pyridoxine is allowed as treatment for a positive PPD, with permission of study chair). Concurrent Treatment: Excluded: Radiation therapy to study marker lesions. Patients with the following prior condition are excluded: Neuropsychiatric history. Prior Medication: Excluded: Any anti-KS therapy within 21 days prior to study entry. Prior systemic therapy with any anthracycline (including liposomal anthracyclines), vincristine, or bleomycin. Any investigational drug (other than those available through Treatment IND and used for FDA-sanctioned purposes) within 14 days prior to study entry. PER AMENDMENT 11/29/95: No more than 2 cycles of any systemic chemotherapy for Kaposi's sarcoma.
Sites / Locations
- Alabama Therapeutics CRS
- USC CRS
- UCLA CARE Center CRS
- Ucsf Aids Crs
- University of Colorado Hospital CRS
- Univ. of Miami AIDS CRS
- Queens Med. Ctr.
- Univ. of Hawaii at Manoa, Leahi Hosp.
- Northwestern University CRS
- Rush Univ. Med. Ctr. ACTG CRS
- Indiana Univ. School of Medicine, Infectious Disease Research Clinic
- Bmc Actg Crs
- Beth Israel Deaconess - East Campus A0102 CRS
- Massachusetts General Hospital ACTG CRS
- Washington U CRS
- SUNY - Buffalo, Erie County Medical Ctr.
- Memorial Sloan-Kettering Cancer Ctr.