跳至主要内容
临床试验/NCT06461689
NCT06461689已完成不适用

Comparison of Changes in Tumor Burden (Toral Tumor Volume [TMTV] and Total Lesion Activity [TLA]) in 68Ga-PSMA-11 PET/CT and 177Lu-PSMA SPECT/CT in the Monitoring of Metastatic Castration-resistant Prostate Cancer Treated With 177Lutetium-PSMA-617

Central Hospital, Nancy, France2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年12月31日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
80
试验地点
2
主要终点
Measurement of TLA (total lesion activity)

研究概览

简要总结

To demonstrate the prognostic value of using post-therapy 177Lu-PSMA SPECT/CT versus 68Ga-PSMA-11 PET/CT in mCPRC patients progressing despite chemotherapy and treated with 177Lu-PSMA.

详细描述

Since few years, therapy by 177Lu-PSMA in nancy hospital began. A lot's of datas were collected. Prostate cancer is the number one killer in france and this is very important to find a diagnostic tool.

The hypothesis of this study is to demonstrate the prognostic value of using post-therapy 177Lu-PSMA SPECT/CT versus 68Ga-PSMA-11 PET/CT in mCPRC patients progressing despite chemotherapy and treated with 177Lu-PSMA.

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

  • patient who received a dose of 177lu-PSMA
  • patient who had imaging by 68Ga-PSMA
  • patient treated in Nancy hospital for its cancer prostate

排除标准

  • no social security
  • no acceptation to participating in retrospective study

研究组 & 干预措施

patient treated as part of mCPRC

All patients treated with 177Lu-PSMA had post-therapy 68Ga-PSMA PET and 177Lu-PSMA-617 SPECT/CT.

干预措施: 177Lu-PSMA-617 (Drug)

结局指标

主要结局

Measurement of TLA (total lesion activity)

时间窗: 12 months

Measurement of TLA (total lesion activity) on 68Ga-PSMA-11 PET/CT (pre-treatment, after 4th treatment and after 6th treatment) and on SPECT/CT (after each treatment).

Measurement of TMTV (total metabolic tumor volume)

时间窗: 12 months

Measurement of TMTV (total metabolic tumor volume) on 68Ga-PSMA-11 PET/CT (pre-treatment, after 4th treatment and after 6th treatment) and on SPECT/CT (after each treatment).

次要结局

未报告次要终点

研究者

发起方
Central Hospital, Nancy, France
申办方类型
Other
责任方
Principal Investigator
主要研究者

BOURSIER Caroline

Principal Investigator

Central Hospital, Nancy, France

研究点 (2)

Loading locations...

相似试验