EPOCH and Rituximab to Treat Non-Hodgkin's Lymphoma in Patients With HIV Infection
2期
已完成
NCT00006436
| 适应症 | Lymphoma, AIDS-related, Lymphoma, Large B-Cell, Diffuse |
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| 分期 | 2期 |
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| 申办方 | National Cancer Institute (NCI) |
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| 状态 | 已完成 |
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| 受试者人数 | 68 人 |
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| 干预(药物) | Rituximab, Filgrastim, EPOCH |
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| 开始日期 | 2001年1月29日 |
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| 完成日期 | 2020年11月30日 |
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| 结果公布日 | 2022年6月28日 |
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摘要
Background: * Human immunodeficiency virus (HIV)-infected patients have a weakened immune system, and chemotherapy, which is used to treat lymphoma, probably causes further damage to the immune system. * Limiting the amount of immune damage due to chemotherapy might decrease the number of infections and the risk of developing cancer in the future in HIV-infected patients with non-Hodgkin's lymphoma. Objectives: * To determine whether reducing the total amount of chemotherapy using a specific combination of drugs called EPOCH-R (etoposide, doxorubicin, vincristine, cyclophosphamide and rituximab) will rid the body of lymphoma quickly while decreasing the risk of infections and future cancers. * To determine whether the lymphoma will remain undetectable for at least one year if treatment is stopped one cycle after the patient enters remission. Eligibility: -Patients with non-Hodgkin's lymphoma and HIV infection 4 years of age and older who have not been treated previously with rituximab or cytotoxic chemotherapy. Design: * Patients receive EPOCH-R in 3-week treatment cycles for at least three and no more than six cycles. * The lymphoma is evaluated using computed tomography (CT) and
Median Progression Free Survival (PFS)
The participants were followed for a median of 15.4 years. · years
| Arm 1-Combination Chemo and Biological Therapy | 13.8 years |
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Progression Free Survival at 1 Year
1 year · percentage of participants
| Arm 1-Combination Chemo and Biological Therapy | 79.1 percentage of participants |
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