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临床试验/NCT02745496
NCT02745496已完成不适用

Multiparametric Magnetic Resonance Imaging Characterization and Guided Biopsy of the Prostate in Men Suspected of Having Prostate Cancer

University of Dundee1 个研究点 分布在 1 个国家目标入组 603 人开始时间: 2014年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
603
试验地点
1
主要终点
Number of prostate cancers detected by MP-MRI when compared to gold standard prostatectomy specimen

研究概览

简要总结

The clinical trial aims to address the critical challenge of differentiating aggressive from indolent prostate cancers by correlating prospectively collected MultiParametric (MP) Magnetic Resonance Imaging (MRI) data (index test) with the histopathology of radical prostatectomy specimens (reference standard).

The study design incorporates pre-biopsy MRI, routine standard of care Transrectal Ultrasound guided (TRUS) biopsies and MRI/Ultrasound (US) image fusion techniques to guide biopsies to the suspicious areas identified by MRI.

The hypothesis is that MP-MRI will allow pre-treatment determination of prostate cancer aggressiveness and MRI/US image fusion is expected to accurately co-locate cancer foci within the prostate gland for guiding biopsies.

Pre-treatment prediction of Gleason grade as a marker of cancer aggressiveness will better inform clinicians and patients to improve risk stratification and facilitate decision making on subsequent treatment.

Image fusion will allow accurate targeting of the most suspicious areas on MP-MRI for biopsy, which could obviate the need for multiple biopsies.

详细描述

There is preliminary evidence suggesting that MultiParametric Magnetic Resonance Imaging (MP-MRI) can be a marker for prostate cancer (PCa) aggressiveness and could be used to plan treatment. Gleason grade (GG) is a critical predictor of the aggressiveness of PCa, but in up to one in three men, the histology of radical prostatectomy specimens is different from the histology of Transrectal Ultrasound (TRUS)-guided biopsies. This discrepancy contributes to- and is a sign of- poor risk stratification of men with localised PCa.

The research aims to answer the following questions:

  1. Can image-fusion techniques allow investigators to reliably target abnormal areas seen on MP-MRI?
  2. How reliable is pre-biopsy MP-MRI in correctly predicting aggressive disease?

The investigators envisage that MP-MRI information will reduce unnecessary biopsies and over-detection of indolent PCa, while improving the detection of aggressive disease.

Primary Objectives

研究设计

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

入排标准

年龄范围
40 Years 至 75 Years(Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •Males between the age of 40-75 at referral
  • •With at least 10 years life expectancy
  • •With clinically localised PCa: Prostate Specific Antigen (PSA) ≤20 ng/ml
  • •And/or abnormal Digital Rectal Examination (DRE) but < T3 disease
  • •Ability to informed consent

排除标准

  • •Unable to give informed consent
  • •Prior prostatic biopsy within 12 months
  • •Contraindications to biopsy
  • •Poor general health and life expectancy < 10 years
  • •Previous diagnosis of acute prostatitis within 12 months
  • •History of prostate cancer
  • •Prior transurethral prostatectomy
  • •Contraindications to MRI (cardiac pacemakers, allergic reaction to gadolinium based contrast, renal function with baseline eGRF 30 ml/min, intracranial clips, claustrophobia)
  • •Previous hip replacement

研究组 & 干预措施

TRUS Biopsy

Other

Standard of Care Treatment

干预措施: TRUS Biopsy (Procedure)

TRUS/FUSION Biopsy

Other

Interventional Treatment

干预措施: TRUS/FUSION Biopsy (Procedure)

结局指标

主要结局

Number of prostate cancers detected by MP-MRI when compared to gold standard prostatectomy specimen

时间窗: 5 years from first recruitment

Number of prostate cancers detected by MP-MRI when compared to gold standard

Number of clinically significant cancers detected by MP-MRI when compared to gold standard prostatectomy specimen

时间窗: 5 years from first recruitment

The definition of clinically significant disease will be based on the pathologic assessment of radical prostatectomy (RP) specimen and will include the presence of any the following three prognostic factors: o Gleason grade \>= 7 with pattern 4 or/and 5 Maximum cancer focus size more than 6mm measured in the axial plane Presence of extracapsular extension (ECE)

次要结局

  • Number of significant cancer detected in each randomised group, namely intervention group (TRUS/FUSION biopsy) versus standard of care (TRUS biopsy)(5 years from first recruitment)
  • Number of cancer detected in each randomised group, namely intervention group (TRUS/FUSION biopsy) versus standard of care (TRUS biopsy)(5 years from first recruitment)
  • Safety outcomes(death, post biopsy pain, bleeding, sepsis and hospitalization) of intervention (biopsy) in each of the two randomised groups.(4 years from first recruitment)
  • Comparison of MRI negative standard of care TRUS guided biopsies with MRI positive TRUS histopathology to facilitate analysis of diagnostic accuracy of MRI in men suspected with target condition.(5 years from first recruitment)

研究者

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

Ghulam Nabi

Professor in Surgical Uro-oncology

University of Dundee

研究点 (1)

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