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临床试验/NCT07624838
NCT07624838招募中不适用

Real-life Experience of Brentuximab Vedotin Plus CHP as First-line Treatment of CD30+ Peripheral T-cell Lymphomas in Spain

Grupo Español de Linfomas y Transplante Autólogo de Médula Ósea37 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2026年2月15日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
100
试验地点
37

研究概览

简要总结

The goal of this observational study is to evaluate how well brentuximab vedotin plus cyclophosphamide, doxorubicin, and prednisone (CHP) works and how safe it is when used as first-line treatment in adults with CD30-positive peripheral T-cell lymphoma in Spain during routine clinical care.

The main questions this study aims to answer are:

  • How long do participants live without their lymphoma getting worse after starting treatment?
  • How well does this treatment reduce or eliminate the lymphoma?
  • How long do participants live after receiving this treatment?
  • What side effects do participants experience, including nerve problems and low white blood cell counts?

Participants have already received brentuximab vedotin plus CHP as part of their usual medical care. Researchers will collect information from existing medical records to better understand treatment outcomes and safety in real-world clinical practice across multiple centers in Spain.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of CD30-positive peripheral T-cell lymphoma, including anaplastic large cell lymphoma (ALK-positive, ALK-negative, breast implant-associated), peripheral T-cell lymphoma not otherwise specified, angioimmunoblastic T-cell lymphoma, hepatosplenic T-cell lymphoma, or enteropathy-associated T-cell lymphoma.
  • Patients 18 years of age or older at the time of treatment with BV-CHP.
  • Patients treated with brentuximab vedotin plus CHP as first-line therapy between January 2019 and September 2024

排除标准

  • Patients who have received prior treatment for their lymphoma
  • Patients who have received the combination as part of a clinical trial.

研究者

发起方
Grupo Español de Linfomas y Transplante Autólogo de Médula Ósea
申办方类型
Other
责任方
Sponsor

研究点 (37)

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