BENITIONSClinical Trial Intelligence

BV-CHEP Chemotherapy for Adult T-cell Leukemia or Lymphoma

2期 已完成 NCT03264131

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)

18 weeks · Participants

Open-label, Multicenter, Single-Arm10 Participants
Open-label, Multicenter, Single-Arm4 Participants
Open-label, Multicenter, Single-Arm2 Participants

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。