Randomized, Comparative Trial of DOX-SL (Stealth Liposomal Doxorubicin Hydrochloride) Versus Bleomycin and Vincristine in the Treatment of AIDS-Related Kaposi's Sarcoma

Last updated: June 23, 2005
Sponsor: Sequus Pharmaceuticals
Overall Status: Completed

Phase

3

Condition

Hiv Infections

Kaposi's Sarcoma

Sarcoma

Treatment

N/A

Clinical Study ID

NCT00002105
134B
LTI-30-11
  • Ages > 18
  • All Genders

Study Summary

To determine the efficacy of Stealth liposomal doxorubicin hydrochloride (DOX-SL) in the treatment of moderate to severe AIDS-related Kaposi's sarcoma (KS) by comparison with the established therapy BV (bleomycin/vincristine). To evaluate the safety and tolerance of DOX-SL compared to BV in a population of AIDS patients with moderate to severe KS.

Eligibility Criteria

Inclusion

Inclusion Criteria

Concurrent Medication:

Allowed:

  • Prophylaxis for PCP, cryptococcal, and herpes infections, and antiretroviral therapy (e.g., AZT, ddC, ddI) provided these doses have been stable for at least 1 month.

  • Maintenance therapy for tuberculosis, fungal, and herpes infections.

  • Therapy for new episodes of tuberculosis, fungal, and herpes infection except with potentially myelotoxic chemotherapy.

  • Foscarnet for cytomegalovirus infection.

  • Erythropoietin.

Patients must have:

  • Biopsy-proven, progressive, AIDS-related Kaposi's sarcoma, with any of the following:

  • At least 15 mucocutaneous lesions.

  • Six or more new lesions in the prior month.

  • Documented visceral disease with at least five accessible cutaneous lesions.

  • Documented anti-HIV antibody.

  • No active opportunistic infection with mycobacteria, cytomegalovirus, toxoplasma, Pneumocystis carinii, or other microorganisms (if REQUIRING treatment with myelotoxic drugs).

  • Life expectancy > 4 months.

NOTE:

  • Patients who fail the BV combination or who relapse are eligible to enter the Liposome Technology open trial using DOX-SL alone.

Exclusion Criteria

Co-existing Condition:

Patients with the following symptoms or conditions are excluded:

  • Clinically significant cardiac disease.

  • Confusion, disorientation, CNS symptoms, or peripheral neuropathy.

Concurrent Medication:

Excluded:

  • Other cytotoxic chemotherapy.

  • Colony-stimulating factors.

  • Ganciclovir.

Patients with the following prior conditions are excluded:

  • Prior neoplasms treated with extensive chemotherapy that, in the investigator's opinion, has led to irreversibly compromised bone marrow function.

  • History of idiosyncratic or allergic reaction to anthracyclines, bleomycin, or vincristine.

  • History of major psychiatric illness.

Prior Medication:

Excluded:

  • Cytotoxic chemotherapy or interferon therapy within the past 4 weeks.

  • More than one prior cycle of bleomycin/vincristine at any time.

Prior Treatment:

Excluded:

  • Radiation or electron beam therapy within the past 3 weeks.

Study Design

Total Participants: 220
Study Start date:
Estimated Completion Date:

Study Description

Patients are randomized to receive either DOX-SL or the BV combination. Infusions are given on day 1 and every 3 weeks for a total of six cycles. Kaposi's sarcoma lesions are evaluated prior to every cycle, at the end of the last treatment cycle, and 4 weeks following the end of the last treatment. Patients who respond to therapy will be followed every 2 months for up to 1 year. Patients must agree to have one or more representative KS lesions biopsied.

Connect with a study center

  • Beth Israel Hosp

    Boston, Massachusetts 02215
    United States

    Site Not Available

  • Mount Sinai Med Ctr

    New York, New York 10029
    United States

    Site Not Available

  • Twelve Oaks Hosp

    Houston, Texas 77074
    United States

    Site Not Available

  • Virginia Mason Research Center / Clinical Trial Unit

    Seattle, Washington 98101
    United States

    Site Not Available

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