Multiparametric Ultrasound Imaging in Prostate Cancer
Primary Purpose
Prostate Cancer, Prostatic Neoplasms
Status
Unknown status
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
SonoVue
Sponsored by
About this trial
This is an interventional diagnostic trial for Prostate Cancer focused on measuring multiparametric ultrasound, prostate cancer, contrast ultrasound, CEUS, radical prostatectomy
Eligibility Criteria
Inclusion Criteria:
- age ≥ 18 years
- biopsy proven prostate carcinoma
- planned treatment by (robot laparoscopic) radical prostatectomy
- signed informed consent
Exclusion Criteria:
- Chemotherapy, radiotherapy or focal therapy of the prostate for prostate cancer
- Hormonal therapy for prostate cancer within last six months
- History of any clinically evidence of cardiac right-to-left shunts
- Receives treatment that includes dobutamine
- Severe pulmonary hypertension (pulmonary artery pressure >90 mmHg) or uncontrolled systemic hypertension or respiratory distress syndrome
- Has any medical condition or other circumstances which would significantly decrease the chances of obtaining reliable data, achieving study objectives, or completing the study
- Is incapable of understanding the language in which the information for the patient is given
Sites / Locations
- AMC University HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Experimental: Single Arm
Arm Description
All consenting patients will undergo mpUS imaging prior to surgery with the ultrasound contrast agent Sonovue for the CEUS specific mode.
Outcomes
Primary Outcome Measures
Validation of mpUS
Predictive accuracy in terms of sensitivity and specificity of mpUS imaging in the detection and localization of prostate cancer by qualitatively and semi-quantitatively correlation of mpUS imaging to corresponding radical prostatectomy histopathology
Secondary Outcome Measures
Differences in mpUS parameters between benign and malignant (low-grade and high-grade) prostate tissue
Parameters of mpUS (echogenicity, contrast-agent perfusion, contrast-agent dispersion, contrast-agent velocity, tissuedensity) will be assessed
mpUS and mpMRI comparison
Comparison of predictive accuracy in terms of sensitivity and specificity of mpMRI imaging and mpUS imaging
Full Information
NCT ID
NCT03101176
First Posted
March 23, 2017
Last Updated
January 16, 2019
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Collaborators
Amsterdam UMC, location VUmc
1. Study Identification
Unique Protocol Identification Number
NCT03101176
Brief Title
Multiparametric Ultrasound Imaging in Prostate Cancer
Official Title
Multiparametric Ultrasound (mpUS) as Imaging Modality for the Detection and Localization of Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
January 2019
Overall Recruitment Status
Unknown status
Study Start Date
September 7, 2017 (Actual)
Primary Completion Date
September 1, 2022 (Anticipated)
Study Completion Date
September 1, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Collaborators
Amsterdam UMC, location VUmc
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Rationale: The current limitations in prostate cancer diagnostics, due to lack of accuracy of the available techniques, lead to over- and undertreatment for a significant fraction of patients with prostate cancer. Multiparametric ultrasound (mpUS), a new imaging modality combining different ultrasound parameters, heralds the potential for an accurate imaging-based diagnostic approach accessible to the community at large but formal validation of mpUS against final pathology results are still lacking.
Objective: To validate mpUS as imaging modality for detection and localization of prostate cancer by direct correlation with histopathology of radical prostatectomy specimens
Detailed Description
Systematic transrectal ultrasound (TRUS)-guided biopsies in men with a clinical suspicion of prostate cancer, based on digital rectal examination (DRE) and/or prostate-specific antigen (PSA) has been the diagnostic strategy for years. However, this method has known limited sensitivity and risks, as many men without cancer undergo unnecessary biopsies, clinically insignificant cancers are often detected while significant cancers are missed or under-graded and the biopsy procedure itself carries discomfort and morbidity. Prostate imaging capable of identifying clinically significant disease for targeted biopsy with high accuracy and efficiency is thus of importance. mpMRI (multiparametric magnetic resonance imaging) and mpMRI-targeted biopsies are being increasingly used, and they have improved the ability to detect clinically significant cancers, while reducing the diagnosis of insignificant cancers compared to TRUS-guided biopsies. Nevertheless, mpMRI has been limited by inter-reader variability, high level of expertise requirements and heterogeneity in definitions while mpMRI-targeted biopsies alone still misses clinical significant cancers revealed by TRUS-guided biopsies.
There is an ongoing search for new cost-effective, manageable imaging technologies for adequate prostate cancer diagnosis. Various ultrasound modalities are in development striving to increase cancer detection among which contrast-enhanced ultrasound (CEUS) and elastography. Preliminary results of a multiparametric ultrasound (mpUS) approach, combining these different ultrasound modalities, seem promising. The number and quality of studies available, however, is relatively low, emphasizing the need for further work to define the role of mpUS.
This is an investigator-initiated, prospective in-vivo validation study in humans to validate mpUS as imaging modality for detection and localization of prostate cancer by direct correlation with histopathology. Biopsy-proven prostate cancer patients scheduled for radical prostatectomy will be approached and consented to enter this study. Information about the study will be provided both verbally and in written form.
Participants will undergo a mpUS imaging prior to their surgery. For the contrast enhanced mode of the mpUS an additional infusion of an ultrasound contrast agent through an intravenous cannula will be used during transrectal ultrasound scanning for the purpose of the study.
The mpUS imaging data will be evaluated qualitatively and semi-quantitatively using parametric maps by prostate ultrasound experts blinded for radical prostatectomy histopathology. Histopathology will be evaluated qualitatively by an uro-pathologist blinded for mpUS imaging results. Hence, imaging data will be correlated with histopathology in a blinded fashion using a 3D registration system and 3D reconstruction model. Predictive accuracy of mpUS imaging for detection and localization of prostate cancer on histopathology will be analyzed.
At a later stage, a mpUS classifier, most optimally combining the most relevant ultrasound parameters of each modality in one single resulting mpUS parameter will be developed. Furthermore, the additional clinical value of mpUS imaging in prostate cancer diagnostics will be determined by comparing mpUS results with that of available mpMRI data. mpMRI imaging data will be evaluated by an uro-radiologist using the PI-RADS (Prostate Imaging Reporting and Data System) criteria blinded for radical prostatectomy results.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer, Prostatic Neoplasms
Keywords
multiparametric ultrasound, prostate cancer, contrast ultrasound, CEUS, radical prostatectomy
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental: Single Arm
Arm Type
Experimental
Arm Description
All consenting patients will undergo mpUS imaging prior to surgery with the ultrasound contrast agent Sonovue for the CEUS specific mode.
Intervention Type
Drug
Intervention Name(s)
SonoVue
Other Intervention Name(s)
sulphur hexafluoride
Intervention Description
The ultrasound contrast agent used for the CEUS specific ultrasound mode
Primary Outcome Measure Information:
Title
Validation of mpUS
Description
Predictive accuracy in terms of sensitivity and specificity of mpUS imaging in the detection and localization of prostate cancer by qualitatively and semi-quantitatively correlation of mpUS imaging to corresponding radical prostatectomy histopathology
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Differences in mpUS parameters between benign and malignant (low-grade and high-grade) prostate tissue
Description
Parameters of mpUS (echogenicity, contrast-agent perfusion, contrast-agent dispersion, contrast-agent velocity, tissuedensity) will be assessed
Time Frame
5 years
Title
mpUS and mpMRI comparison
Description
Comparison of predictive accuracy in terms of sensitivity and specificity of mpMRI imaging and mpUS imaging
Time Frame
5 years
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age ≥ 18 years
biopsy proven prostate carcinoma
planned treatment by (robot laparoscopic) radical prostatectomy
signed informed consent
Exclusion Criteria:
Chemotherapy, radiotherapy or focal therapy of the prostate for prostate cancer
Hormonal therapy for prostate cancer within last six months
History of any clinically evidence of cardiac right-to-left shunts
Receives treatment that includes dobutamine
Severe pulmonary hypertension (pulmonary artery pressure >90 mmHg) or uncontrolled systemic hypertension or respiratory distress syndrome
Has any medical condition or other circumstances which would significantly decrease the chances of obtaining reliable data, achieving study objectives, or completing the study
Is incapable of understanding the language in which the information for the patient is given
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
H. Wijkstra, Prof dr ir
Phone
+31 20 5666379
Email
h.wijkstra@amc.uva.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
H. Wijkstra, Prof dr ir
Organizational Affiliation
AMC University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
AMC University Hospital
City
Amsterdam
ZIP/Postal Code
1105 AZ
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
H. Wijkstra, Prof dr ir
Phone
+31 20 5666379
Email
h.wijkstra@amc.uva.nl
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
23485507
Citation
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Results Reference
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Citation
Ukimura O, Coleman JA, de la Taille A, Emberton M, Epstein JI, Freedland SJ, Giannarini G, Kibel AS, Montironi R, Ploussard G, Roobol MJ, Scattoni V, Jones JS. Contemporary role of systematic prostate biopsies: indications, techniques, and implications for patient care. Eur Urol. 2013 Feb;63(2):214-30. doi: 10.1016/j.eururo.2012.09.033. Epub 2012 Sep 25.
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27543165
Citation
Borghesi M, Ahmed H, Nam R, Schaeffer E, Schiavina R, Taneja S, Weidner W, Loeb S. Complications After Systematic, Random, and Image-guided Prostate Biopsy. Eur Urol. 2017 Mar;71(3):353-365. doi: 10.1016/j.eururo.2016.08.004. Epub 2016 Aug 17.
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PubMed Identifier
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Citation
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PubMed Identifier
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Citation
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Multiparametric Ultrasound Imaging in Prostate Cancer
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