BV-CHEP Chemotherapy for Adult T-cell Leukemia or Lymphoma
| 适应症 | Lymphoma, Adult T-Cell Leukemia/Lymphoma, Lymphatic Diseases |
|---|---|
| 分期 | 2期 |
| 申办方 | UNC Lineberger Comprehensive Cancer Center |
| 状态 | 已完成 |
| 受试者人数 | 16 人 |
| 干预(药物) | Brentuximab Vedotin, CHEP |
| 开始日期 | 2018年10月11日 |
| 完成日期 | 2023年12月15日 |
| 结果公布日 | 2025年2月10日 |
摘要
Adult T-cell leukemia/lymphoma (ATLL) is a rare form of cancer found mostly among people from the Caribbean islands, Western Africa, Brazil, Iran, and Japan. Most cases of this disease in the United States occur along the East Coast due to emigration from the Caribbean islands. There is currently no standard treatment for ATLL. Research shows that patients who go into first time remission (respond completely or partially to treatment) and have a bone marrow transplant have the best outcomes. Traditional chemotherapy treatments have generally not worked well in patients with ATLL. Additionally, not all patients will be eligible for a bone marrow transplant. The purpose of this study is to see how well individuals with ATLL respond to an investigational cancer treatment. This investigational treatment combines a drug called brentuximab vedotin with a standard chemotherapy treatment made up of cyclophosphamide, doxorubicin, etoposide, and prednisone. This treatment is considered investigational because it is not approved by the United States Food and Drug Administration (FDA) for the treatment of ATLL. Brentuximab vedotin, also known as Adcetris, is approved by the United States Food
Complete Response Rate After 2-6 Cycles of Brentuximab Vedotin in Combination With Cyclophosphamide, Doxorubicin, Etoposide, and Prednisone (BV-CHEP)
| Open-label, Multicenter, Single-Arm | 10 Participants |
|---|---|
| Open-label, Multicenter, Single-Arm | 4 Participants |
| Open-label, Multicenter, Single-Arm | 2 Participants |
在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文
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