NCT03525665已完成不适用
Study on the Role of FDG-PET in Patients With Follicular Lymphoma at Time of Relapse/Progression
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 175
- 试验地点
- 27
- 主要终点
- PFS
研究概览
简要总结
The study is designed as a retrospective analysis of patients with relapsed/refractory FL identified by the hematological centers of Italy.
详细描述
The study does not require any intervention on the patient, but it involves the simple collection of data that are already present in the medical record. Since this is a retrospective study, it will not require further analysis or diagnostic investigations than those already made.
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
- 否
入选标准
- •Patients with initial diagnosis of follicular lymphoma since 2001
- •Histological confirmation of follicular lymphoma, grade I, II, III according to WHO 2008 classification, at the time of initial diagnosis
- •Systemic first-line treatment with immuno-chemotherapy
- •PET availability at the time of response after first-line treatment (optional)
- •Clinical and radiological evidence of FL relapse or progression
- •Histological confirmation of relapse (strongly recommended)
- •PET availability of at the time of relapse/progression and images available for central assessment
- •Availability of clinical, laboratory and therapeutic treatment data at the time of initial diagnosis and relapse/progression
- •Follow up of at least 12 months after relapse/progression
排除标准
- 未提供
结局指标
主要结局
PFS
时间窗: 24 months
Progression free survival from time of relapse/progression
次要结局
- OS(24 months)
研究者
研究点 (27)
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