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临床试验/NCT06866782
NCT06866782招募中不适用

European Registry of Next Generation Imaging in Advanced Prostate Cancer

Fundacio Puigvert23 个研究点 分布在 8 个国家目标入组 600 人开始时间: 2024年9月17日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
600
试验地点
23
主要终点
Proportion of patients requiring NGI, conventional imaging, or a combination of both imaging tools.

研究概览

简要总结

The RING study is a European registry collecting real-world data on advanced prostate cancer (APC) imaging. It aims to evaluate the role of next-generation imaging (NGI), such as PET/CT and whole-body MRI, in detecting and monitoring the disease compared to conventional imaging.

Men aged 18 or older with histologically confirmed prostate cancer are eligible to participate in the study if they require imaging to assess potential metastases, either at diagnosis or after relapse and sign a consent form.

Patients will receive standard care with no experimental treatments. Imaging and treatment decisions will follow routine clinical practice. Data will be collected from medical records and analysed for research. This study will help doctors understand when NGI should be used, how it affects treatment decisions, and its impact on patient outcomes.

详细描述

This registry is intended to collect real-world data on patient demographics, medical history, clinical endpoints, histological tumour characteristics and imaging explorations of the patients with prostate cancer at high risk for harbouring metastatic deposits at the hormone-sensitive stage, who require imaging exploration (conventional, NGI, or their combination) either at the diagnostic workup of a "naïve" patient or at biochemical relapse/progression after local treatment.

Stage 1: cross-sectional observation

  1. To identify the proportion of patients for whom an imaging work-up with NGI at baseline may result beneficial, according to physician criteria.

  2. Assess management prompted by NGI vs. conventional imaging in usual clinical practice.

  3. To identify the proportion of patients for whom conventional imaging is considered informative enough for making a clinical decision, according to physician criteria.

  4. Stratification of metastatic prostate cancer patients by the number, volume, and location of deposits, according to the different imaging tools employed.

  5. Reclassification of HSPC (M0 vs low vs. high volume) based on NGI respect to CI when both imaging modalities are used. Stage 2: longitudinal observation

  6. Evaluation of survival outcomes and their relationship with the imaging pathway undertaken (overall and per subgroup of imaging modality). 2. Identification of prognostic factors related to treatment response and disease progression.

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
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •Adult male patients (≥18 years with no upper age limit).
  • •Histologically proven prostate cancer.
  • •Patients who require imaging exploration (conventional, Next-Generation Imaging (NGI), or their combination) at high risk for harbouring metastatic deposits at the hormone-sensitive stage, either at the diagnostic workout of a "naïve" patient or at biochemical relapse/progression after local treatment.
  • •Patients who authorize their participation in the study by signing a written informed consent form (ICF).

排除标准

  • •Patients participating in other interventional or non-interventional study which requires NGI as a triage test for metastatic assessment.
  • •Patients with evidence of any other clinically significant disease or condition which in the opinion of the investigator discourages their participation in the study.
  • •Patients who will not be able to complete the study.

结局指标

主要结局

Proportion of patients requiring NGI, conventional imaging, or a combination of both imaging tools.

时间窗: 4 - 6 weeks

Number of patients who require NGI, conventional imaging, or a combination of both imaging tools with the respect to local protocols

Proportion of patients with a change of treatment determined by the imaging test result, when multiple imaging tests have been realized

时间窗: 4-6 weeks

Number of patients who received multiple imaging tests for whom the result of the particular imaging test has lead to the change in management

次要结局

未报告次要终点

研究者

发起方
Fundacio Puigvert
申办方类型
Other
责任方
Principal Investigator
主要研究者

Francesco Sanguedolce

Chief Investigator

Fundacio Puigvert

研究点 (23)

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