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Spots Global Cancer Trial Database for Comparison of Liposomal Doxorubicin Used Alone or in Combination With Bleomycin Plus Vincristine in the Treatment of Kaposi's Sarcoma in Patients With AIDS

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Trial Identification

Brief Title: Comparison of Liposomal Doxorubicin Used Alone or in Combination With Bleomycin Plus Vincristine in the Treatment of Kaposi's Sarcoma in Patients With AIDS

Official Title: Comparison Study of Liposomal Doxorubicin With or Without Bleomycin and Vincristine for the Treatment of Advanced AIDS-Associated Kaposi's Sarcoma

Study ID: NCT00001059

Study Description

Brief Summary: To evaluate the safety and efficacy of liposomal doxorubicin hydrochloride ( DOX-SL ) alone or in combination with bleomycin and vincristine in the long-term treatment of AIDS-related Kaposi's sarcoma. To determine whether the 3-drug combination enhances progression-free survival and quality of life. Liposomal formulations of chemotherapeutic agents increase drug accumulation in tumors, which permits disease palliation at relatively low doses and thus decreases some of the dose-limiting toxicity. Multi-agent therapy is considered to be more effective than single-agent therapy; therefore, DOX-SL will be combined with bleomycin and vincristine.

Detailed Description: Liposomal formulations of chemotherapeutic agents increase drug accumulation in tumors, which permits disease palliation at relatively low doses and thus decreases some of the dose-limiting toxicity. Multi-agent therapy is considered to be more effective than single-agent therapy; therefore, DOX-SL will be combined with bleomycin and vincristine. Patients are randomized to receive intravenous DOX-SL alone or in combination with vincristine/bleomycin every 2 weeks. Filgrastim ( granulocyte colony-stimulating factor; G-CSF ) may be given as needed for neutropenia. AS PER AMENDMENT 11/7/96: Based on interim review data, it is recommended that subjects receiving DOX-SL plus vincristine/bleomycin have vincristine/bleomycin discontinued and receive DOX-SL alone unless, in the opinion of the treating physician, they are benefitting from the DOX-SL plus vincristine/bleomycin regimen.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Alabama Therapeutics CRS, Birmingham, Alabama, United States

USC CRS, Los Angeles, California, United States

UCLA CARE Center CRS, Los Angeles, California, United States

Ucsf Aids Crs, San Francisco, California, United States

University of Colorado Hospital CRS, Aurora, Colorado, United States

Univ. of Miami AIDS CRS, Miami, Florida, United States

Queens Med. Ctr., Honolulu, Hawaii, United States

Univ. of Hawaii at Manoa, Leahi Hosp., Honolulu, Hawaii, United States

Northwestern University CRS, Chicago, Illinois, United States

Rush Univ. Med. Ctr. ACTG CRS, Chicago, Illinois, United States

Indiana Univ. School of Medicine, Infectious Disease Research Clinic, Indianapolis, Indiana, United States

Bmc Actg Crs, Boston, Massachusetts, United States

Beth Israel Deaconess - East Campus A0102 CRS, Boston, Massachusetts, United States

Massachusetts General Hospital ACTG CRS, Boston, Massachusetts, United States

Washington U CRS, St. Louis, Missouri, United States

SUNY - Buffalo, Erie County Medical Ctr., Buffalo, New York, United States

Memorial Sloan-Kettering Cancer Ctr., New York, New York, United States

Contact Details

Name: Mitsuyasu R

Affiliation:

Role: STUDY_CHAIR

Name: Krown S

Affiliation:

Role: STUDY_CHAIR

Name: Von Roenn JH

Affiliation:

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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