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临床试验/NCT03423303
NCT03423303Enrolling By Invitation不适用

Randomized Population-Based Pragmatic Prostate Cancer Screening Trial Based on PSA, Kallikrein Panel, and MRI

Tampere University2 个研究点 分布在 1 个国家目标入组 17,400 人开始时间: 2018年4月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
17,400
试验地点
2
主要终点
Prostate cancer (PrCa) mortality

研究概览

简要总结

A population-based randomised trial of prostate cancer screening will be carried out. A total of approximately 117,200 men aged 50-63 in Helsinki and Tampere are randomised to intervention (screening) or control arm. A reduction in harms of screening in the form of overdiagnosis is sought, while retaining as much as possible of the mortality benefit (reduction in prostate cancer mortality). Novel methods that have been shown to increase specificity for clinically relevant prostate cancer but never tested in a randomised setting will be employed in screening and diagnostics. The main end-point is prostate cancer mortality at 10 and 15 years of follow-up.

详细描述

Frequent adverse effects have so far tipped the balance of benefits and harms against prostate cancer screening, and therefore the investigators will focus on employing the best possible means for reducing them. The project introduces a novel concept for PC screening that minimises overdiagnosis and overtreatment, while retaining the mortality benefit to shift the balance of screening benefits and harms to a favourable net effect. The strategy for implementation as a randomised screening trial utilises three levels of risk assessment (PSA, kallikrein panel and MRI) before the diagnostic procedure (prostate biopsy), each aimed at eliminating detection of indolent disease. The study hypothesis is that by virtue of the novel three-tiered screening algorithm, the beneficial screening effect (prostate cancer mortality reduction) can be retained, while the overdiagnosis can be largely eliminated. The impact of an integrative approach has never been evaluated - each of the methods has only been assessed in isolation. The breakthrough potential of the proposal lies in combining the three novel approaches and taking them to the forefront of applied research through a randomised trial. The key impact of the study is in defining whether the overall balance of benefits and harms of prostate cancer screening can be reversed by applying the best possible methods to detect only clinically important disease. If the study hypothesis is affirmed, it opens the way to introduction of prostate cancer screening. If the balance of harms and benefits is still unfavourable, the problem of overdiagnosis in prostate cancer may be intractable.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Screening
盲法
None

入排标准

年龄范围
50 Years 至 63 Years(Adult)
性别
Male
接受健康志愿者
是

入选标准

  • •50-63-year-old men (age in 2018) residing in Tampere or Helsinki

排除标准

  • •Prevalent prostate cancer

研究组 & 干预措施

Screening arm

Experimental

Invitation to prostate cancer screening and questionnaires.

干预措施: Prostate cancer screening (Diagnostic Test)

Control arm

No Intervention

Registry-based follow-up and a questionnaire.

结局指标

主要结局

Prostate cancer (PrCa) mortality

时间窗: At 10 years of follow-up.

An intention to screen analysis will be performed, with all men in the groups defined by random allocation, regardless of compliance. Follow-up starts at randomisation, and ends at death. Cox regression will be used with prostate cancer death as the outcome.

次要结局

  • Prostate cancer (PrCa) mortality - secondary analysis(At 10 years of follow-up.)
  • Cumulative incidence of advanced (T3-T4 or M1) prostate cancer(At approximately 5 years of follow-up.)
  • Cumulative incidence of low-risk cancer (Gleason<7)(At approximately 5 years of follow-up.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Anssi Auvinen

Professor

Tampere University

研究点 (2)

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