跳至主要内容
临床试验/NCT07309497
NCT07309497招募中不适用

Pragmatic Geriatric Assessment (pGA) Before Bispecific Antibody and CAR-T-Cell Therapy (GA-ACT Trial) for the Prediction of Toxicity and Outcomes in Older Patients Scheduled for Chimeric Antigen Receptor T-Cell Therapy (CAR-T-Cell-Therapy) or Bispecific Antibody (bsAB) Treatment

University of Zurich2 个研究点 分布在 1 个国家目标入组 208 人开始时间: 2025年12月12日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
208
试验地点
2
主要终点
treatment toxicity

研究概览

简要总结

CAR-T cell or bispecific antibody therapies are a new treatment option for adult patients with aggressive forms of lymphoma or so-called plasma cell diseases ('multiple myeloma', 'plasma cell myeloma') that could not be cured with other, less intensive approaches. However, these are intensive therapies that can be associated with severe and potentially life-threatening side effects. Although there is no age limit for these therapies, we know little about the short- and long-term side effects of these treatments in people of advanced age.

Although a small number of patients in the pivotal studies were even over 80 years old, their number was too small to be able to assess the tolerability and success specifically in people over 65. At present, the treating physicians decide whether and, if so, which patients are considered 'fit' enough for this therapy. An objective assessment of the kind we want to investigate in our study does not currently exist on a regular basis. In this study, we therefore want to use simple clinical methods to investigate the effects of these forms of therapy in different areas of everyday function that are important for people in older age (mobility, memory, self-care skills, nutrition). We want to find out whether these investigations help to predict the risk of severe and/or long-term side effects. Based on the results, a pragmatic geriatric assessment could be introduced as standard before these therapies. Older patients could thus expect an improvement in their quality of life thanks to more predictable risks and side effects. Standardized screening could lead to lower healthcare costs for treatment and aftercare for both forms of therapy.

研究设计

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

入排标准

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

入选标准

  • male or female patients age ≥ 65 years,
  • scheduled for CAR-T-cell or bsAB treatments
  • signed informed consent
  • sufficient knowledge of the German or French language

排除标准

  • inability to understand or sign informed consent
  • refuse to consent

结局指标

主要结局

treatment toxicity

时间窗: From enrollment to 3 month after end of treatment

primary endpoint will be the composite rate of death or any one of ≥ grade 3 toxicity

次要结局

  • health related quality of life(From enrollment to 3 month after end of treatment)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验