Can Significant Prostate Cancer be Detected With a Short Non-contrast Enhanced Biparametric MRI (bpMRI)?
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 1,063
- 试验地点
- 2
- 主要终点
- Diagnostic accuracy of a bp-MRI in detection and ruling out significant PCa in biopsy-naive men
研究概览
简要总结
Our aim is to develop a new diagnostic approach to improve the diagnosis of men suspicious of having significant prostate cancer (sPCa). The current diagnostic technique (standard transrectal ultrasound-guided biopsies [TRUS-bx]) rely on multiple prostate biopsy cores (10-12 samples) and if negative repeated biopsy sessions. This increases both patient complications (severe infections, bleeding and anxiety) and the diagnosis of insignificant cancer causing overtreatment. Still, significant cancers are missed. In addition, worldwide antibiotic-resistant bacteria increase, while effective antibiotics are declining. Thus, a noninvasive diagnostic tool to improve selection of men with clinically suspicion of PCa who need a biopsy from those who can avoid one is strongly needed. Previous studies in our department show that MRI in a selected patient cohort with prior negative TRUS-bx can improve the detection rate of clinically significant PCa and allows for a more accurate assessment of cancer stage and aggressiveness. However, the value of an MRI used as a first-line tool in the diagnostic examination of men in suspicion of PCa is uncertain. Furthermore, a full scale MRI prostate examination recommended by the European Society of Urogenital Radiology includes intravenous contrast-media and multiple sequences. This is both time-consuming and cost full, which reduces its feasibility for more widespread clinical implementation. We believe that a simpler, faster biparametric MRI (bpMRI) using less scan sequences and circumvents intravenous contrast-media and anti-peristaltic drugs would decrease image acquisition time, reduce costs and is sufficient to preserve diagnostic accuracy for sPCa detection in biopsy-naive men. Consequently, we will include biopsy-naive men in a protocol-based research project. The objective is to assess the diagnostic accuracy of bpMRI to rule out sPCa and whether a bpMRI can be used as a diagnostic non-invasive screening tool to 1) improve the diagnosis of sPCa 2) assess cancer aggressiveness 3) increase precision of biopsies and 4) reduce the number of biopsy sessions and cores. We evaluate the clinical significance of the detected cancers and whether bpMRI could be used as a triage test to improve the diagnosis of sPCa and aid in the determination of which men could safely avoid unnecessary biopsies.
This new diagnostic approach has the potential to significantly reduce patient hazards and complications. We aim to reach 1000 included men. We believe that bpMRI used in the clinical decision-making has the potential to change the future management of PCa. However, we still miss the scientific evidence to substantiate its preliminary promising results before this technique can be widely used to benefit all men. This large research project is to the best of our knowledge powered to include the largest patient sample size published within this field.
详细描述
Purpose Our aim is to assess whether a screening bpMRI can be used as a diagnostic non-invasive screening tool to 1) improve the diagnosis of sPCa 2) predict cancer aggressiveness 3) increase precision of biopsies and 4) reduce the number of biopsy sessions and cores.
Trial subjects Subjects are recruited at the Department of Urology, Herlev Gentofte University Hospital. Annually, approx. 1.600 men are referred to the department due to clinical suspicion of PCa. Roughly 1.100 men further proceeds to standard TRUS-bx prostate biopsies. These men are invited to participate as subjects in this study and undergo a bpMRI before biopsies, if they fulfil the inclusion criteria. All subjects provide written informed consent and can withdraw their consent at any time with no consequence in relation to their standard treatment. Intended sample size calculations (power 0•9 and 2-sided significance 0•05) were based on estimates of diagnostic accuracy (sensitivity and specificity) and detection rates by biopsy techniques (SBx and TBx) from prior mpMRI studies assuming prevalence of sPCa of 30%. Target sample size was minimum 600 patient.
Study Design This study is designed as a prospective interventional study. All enrolled patients undergo a screening bpMRI of the prostate within 1-2 weeks after inclusion and prior to biopsies. All MRI data undergo blinded evaluation according to a modified PIRADS version 2 classification from the European Society of Urogenital Radiology (ESUR) 18 by an experienced physician who register and score all suspicious lesions on a five-point scale (1- very low, 2 - low, 3 - intermediate, 4- high and 5 - very high) according to the overall probability of having significant PCa. As the bpMRI protocol does not include dynamic contrast-enhanced (DCE) imaging, scoring of lesions in the peripheral zone relied solely on DWI findings. The bpMRI is within 4-weeks followed by standard 10-core TRUS-bx performed according to current standard practice and blinded to any MRI findings. The TRUS-operator then subsequently reviews the MRI data and rapport on a dedicated workstation in the biopsy room to identify suspicious lesions presented and outlined by the radiologist. Any suspicious lesions are then targeted by additional bpMRI-guided biopsies using bpMRI-TRUS image fusion based software. BpMRI suspicion scores and biopsy results from TRUS-bx and bpMRI-bx are compared.
Furthermore, all enrolled patients are clinically followed for 5 years after the initial biopsies to detect any subsequent diagnosis of PCa, treatment recurrence or metastasis.
MRI image acquisition:
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 85 Years(Adult, Older Adult)
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Age: 18 to 85 years.
- •Clinical suspicion of PCa based on: serum level of prostate-specific-antigen (PSA) from 2.5 ng/ml in two consecutive measurements and/or abnormal diagital rectal examination (DRE).
- •Mental status: Patients must be able to understand the objective of the study.
- •Informed consent: The patient must sign the local Ethics Committee (EC) approved informed consent documents in the presence of the designated staff.
排除标准
- •Previous prostate biopsies.
- •Previous diagnosis of PCa.
- •Acute prostatitis.
- •Contraindications to MRI (cardiac pacemaker, claustrophobia etc).
- •Infection (temperature > 38 degrees Celsius)
- •Hip replacement surgery or other metal implants in the pelvic area.
研究组 & 干预措施
Biparametric MRI before biopsy
Biparametric MRI is a reduced Multiparametric MRI using less scan sequences and no intravenous contrast.
All men will have standard transrectal ultrasound guided biopsies
干预措施: Biparametric MRI before biopsy (Device)
结局指标
主要结局
Diagnostic accuracy of a bp-MRI in detection and ruling out significant PCa in biopsy-naive men
时间窗: 24 months
All included men undergo bp-MRI at inclusion followed by diagnostic standard TRUS biopsies (current diagnostic standard). Men with any suspicious lesions on bpMRI undergo additional bpMRI-guided biopsies (bpMRI-bx) using bpMRI-TRUS image fusion based software. BpMRI suspicion scores and biopsy results ( detection of any PCa and sPCa) from standard TRUS-bx and bpMRI-bx are compared using combined biopsy results as standard reference. Sensitivity and negative predictive value of bpMRI to detect and rule out sPCa will be determined
次要结局
未报告次要终点
研究者
Karen-Cecilie Duus Thestrup
Cand. med.
Herlev Hospital
