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Spots Global Cancer Trial Database for A Phase III Randomized Trial of Low-Dose Versus Standard-Dose mBACOD Chemotherapy With rGM-CSF for Treatment of AIDS-Associated Non-Hodgkin's Lymphoma

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Trial Identification

Brief Title: A Phase III Randomized Trial of Low-Dose Versus Standard-Dose mBACOD Chemotherapy With rGM-CSF for Treatment of AIDS-Associated Non-Hodgkin's Lymphoma

Official Title: A Phase III Randomized Trial of Low-Dose Versus Standard-Dose mBACOD Chemotherapy With rGM-CSF for Treatment of AIDS-Associated Non-Hodgkin's Lymphoma

Study ID: NCT00000658

Study Description

Brief Summary: To determine the impact of dose intensity on tumor response and survival in patients with HIV-associated non-Hodgkin's lymphoma (NHL). HIV-infected patients are at increased risk for developing intermediate and high-grade NHL. While combination chemotherapy for aggressive B-cell NHL in the absence of immunodeficiency is highly effective, the outcome of therapy for patients with AIDS-associated NHL has been disappointing. Treatment is frequently complicated by the occurrence of multiple opportunistic infections, as well as the presence of poor bone marrow reserve, making the administration of standard doses of chemotherapy difficult. A recent study was completed using a low-dose modification of the standard mBACOD (cyclophosphamide, doxorubicin, vincristine, bleomycin, dexamethasone, methotrexate ) treatment. A 46 percent response rate was observed in patients treated with this combination of chemotherapeutic agents, with a number of durable remissions and reduced toxicity when compared to previous experience with more standard treatments. A subsequent study showed similar effectiveness using a lower dose of methotrexate administered on day 15. It is hoped that the use of sargramostim (granulocyte-macrophage colony-stimulating factor; GM-CSF) will improve bone marrow function and allow for administration of a higher dose of chemotherapy.

Detailed Description: HIV-infected patients are at increased risk for developing intermediate and high-grade NHL. While combination chemotherapy for aggressive B-cell NHL in the absence of immunodeficiency is highly effective, the outcome of therapy for patients with AIDS-associated NHL has been disappointing. Treatment is frequently complicated by the occurrence of multiple opportunistic infections, as well as the presence of poor bone marrow reserve, making the administration of standard doses of chemotherapy difficult. A recent study was completed using a low-dose modification of the standard mBACOD (cyclophosphamide, doxorubicin, vincristine, bleomycin, dexamethasone, methotrexate ) treatment. A 46 percent response rate was observed in patients treated with this combination of chemotherapeutic agents, with a number of durable remissions and reduced toxicity when compared to previous experience with more standard treatments. A subsequent study showed similar effectiveness using a lower dose of methotrexate administered on day 15. It is hoped that the use of sargramostim (granulocyte-macrophage colony-stimulating factor; GM-CSF) will improve bone marrow function and allow for administration of a higher dose of chemotherapy. Patients are randomized to one of two treatment groups. Patients are stratified for (1) presence or absence of a prior AIDS diagnosis, (2) Karnofsky performance status of 70 or greater and lower than 70. Treatment includes prophylaxis for meningeal lymphoma and Pneumocystis carinii pneumonia. Patients on low-dose mBACOD who experience neutropenia may be given rGM-CSF until the absolute neutrophil count improves. AZT may be initiated at the completion of chemotherapy for all patients in complete remission at that time. PER AMENDMENT 5/30/95: This trial was closed to accrual on 11/7/94 on the recommendation of the Data and Safety Monitoring Board (DSMB), because the non-significant difference in survival between the 2 treatment groups was not expected to change with further enrollment.

Eligibility

Minimum Age: 12 Years

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

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

Johns Hopkins Adult AIDS CRS, Baltimore, Maryland, United States

Beth Israel Deaconess Med. Ctr., ACTG CRS, Boston, Massachusetts, United States

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

Bmc Actg Crs, Boston, Massachusetts, United States

Washington U CRS, Saint Louis, Missouri, United States

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

Beth Israel Med. Ctr. (Mt. Sinai), New York, New York, United States

NY Univ. HIV/AIDS CRS, New York, New York, United States

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

Univ. of Rochester ACTG CRS, Rochester, New York, United States

Unc Aids Crs, Chapel Hill, North Carolina, United States

Case CRS, Cleveland, Ohio, United States

The Ohio State Univ. AIDS CRS, Columbus, Ohio, United States

Hosp. of the Univ. of Pennsylvania CRS, Philadelphia, Pennsylvania, United States

Pitt CRS, Pittsburgh, Pennsylvania, United States

Contact Details

Name: L Kaplan

Affiliation:

Role: STUDY_CHAIR

Name: AA Levine

Affiliation:

Role: STUDY_CHAIR

Name: DJ Straus

Affiliation:

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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