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MRI and Fusion biopsies K Sahadevan
Consultant Urologist
MRI in Prostate Cancer Diagnosis
Traditionally used for staging purposes 70 to 90% accurate detection of extra capsular disease on
MRI (cornud 2002)
3T MRI, Endorectal coil, MR spectroscpy for improved staging
Currently Diagnostic scan T1,T2, DWI, MRS, DCE Scoring systems Standards of technique
PIRADS
BI-RADS for breast cancer imaging Liberman 2002
ESUR- PIRADS v1, 2012
ESUR-ACR- PIRADS v2, 2015
Hamoen 2015; Metaanalysis Sensitivity 70 to 85 NPV 58 to 95
PIRADS V1 vs V2
Dominant sequence T2W for TZ, DWI for PZ
DCE To downgrade or upgrade PIRADS 3 in PZ
No MRS
New sectoral map
Sectoral map for reporting PIRADS 2
How reliable is MRI?
How reliable is MRI: Heterogeneity Heterogenous studies
Definition of clinically sig disease UCL1: Gleason 4+3 or higher and / or CCL >6mm UCL2: Any Gleason 4 and / or CCL 4mm Epstein criteria +/- ADC <850 mm2/s Gleason score 7 Gleason score 8 PSA >10 ng/ml, PSA density >0.15, clinical stage T2b,
Gleason 4 or 5, total CCL 10 mm Gleason 6–7 with 5% Gleason 4 + either 30% of cores positive
or CCL >8 mm Radiologist experience Variable comparator (extended bx, TR, TP, RRP)
How reliable is MRI?
Futterer 2015 Cancer detection rates of 44% to 87%, NPV 63 to 98%
Ref pts std CSig sens spec PPv NPV
2013 538 fusion G7 94 28 38 91
2015 150 fusion G7, >5% or CCL 8mm
96 50 50 96
2015 115 RRP Epstein 96 46 66 92
PROMIS
Paired cohort, mpMRI follwed by TRUS and template bx
576 pts
TPM detected 40% clinically significant cancers (UCL1)
2% clinically significant cancers missed on MRI
27% may avoid biopsy
UCL1 = Gl 4+3 +/->6mm CCL
Ref sens NPV
MRI 93 89
TRUS 48 74
How reliable is MRI: vs RRP specimen
Delongchamos 2015 14/ 137 (10%) foci of significant cancer (G7/ G6+>0.5ml) missed on mri 4% of tumour missed by targeted biopsy but detected by mrI
Baco 2015 135 pts 5%index lesions (some G6) invisible on MRI 10% index lesions missed on targetted bx
Le 2015 122 pts, 80% index lesion detection 5% targeted bx missed index lesion
Branger 2016: RRP in pts with a negative MRI 17% T3, 14% Primary Gleason 4 or above, 47.5% had secondary Gleason 4 But when MRI expertly re-read, only 4% T3, 4% primary 4
MRI can identify high volume or higher grade tumours in 80-95% of the cases
Evasive lesions!
Targetted biopsies
MR targetted biopsies In bore Not much literature Sensitivities 50 to 80% Expensive, time consuming
Cognitive Less expensive, readily available, do need expertise Variable results but negative sensitivity up to 97% 3D
Software aided
Fusion vs TRUS
Siddiqui 2015: Fusion bx showed 30 higher incidence of high risk 17% lower incidence of low risk cases
Schhots 2015 Metaanalysis approx 2000 pts Higher detection of high risk and lower detection of low risk with
targetted compared to TRUS Sensitivity of MR T bx vs TRUS bx is 91 vs 74%
Wegelin 2016: Systematic TRUS vs Cog Fusion, software fusion, MRI in bore No significant different between modalities, (? In bore >software
fusion>cognitive) Targetted bx higher yield for clinically significant prostate cancer RCT b/w cognitive vs fusion vs in bore on going
Fusion Vs TRUS in RRPSiddiui JAMA
Issues with Fusion
Radiologist Acquisition (angles, pulses, sequences etc) Interpretation (PIRADS)
Urologist Registration/fusion (deformation, position) Identification Needle track/target
Pathologist Inter observer variability
Patient Movement, bowel prep
MRI Fusion: Ideal parameters
Compatibility: In house US probes and with PACS
Suitable for transrectal and trans perineal approaches
Easy workflow and short learning curve
Rigid and elastic registration
Ability to use record needle track
Cost!
MRI/TRUS fusion platforms
Many european and American systems
Usually with own US systems
TR and TP options
Slight variation in physical form
Manual vs robotic arm
Electromagenetic vs visual tracking
Validation studies
Uronav: Philips
Uronav
Support for both transperineal and transrectal biopsy approaches -
Ultrasound-only work flow for guided navigation without the need for pre-biopsy MR data
Display of prior biopsy core locations and data from previous procedures performed with UroNav
Robust, 3D gland segmentation modeling and flexibility to perform dynamic adjustments of the ultrasound segmentation boundary
Elastic (deformable) and rigid registration options -
On-the-fly registration adjustments
Biopsee
Biopsee
Fusion with MRI Spectroscopy, dynamic MRI, PET, PET-CT, SPECT (fusion with any DICOM image type)
3D, elastography, DCE abilities
Automatic 3D ultrasound image acquisition (minimum 1mm slices)
Superb tools for delineating target areas and structures in any image set
Stereotactic biopsy planning module for plotting exact needle paths
Live stereotactic needle navigation with practical guidance tools
Automatic recording of all significant data: exact biopsy coordinates, ultrasound parameters and patient data
Documentation and reporting tool for follow-up
Artemis: Hitachi Aloka
Artemis
Prostate mapping via needle navigation and tracking
Revisit previous sample sites/overlay previous gland volumes
Integrated motion compensation
Automatic recording of all biopsy locations
Automatic 2D to 3D image conversion
BK Fusion BioJet
Triplane Transducer is the only urology transducer that allows you to shift between simultaneous biplane and endfire imaging modes at the touch of a button and without removing the transducer from the patient.
Koelis: available in US
Easote: Virtual navigator
Multiparametric US Sensitivity up to
90%
PPV 50-90%
NPV 60-100%
CEUS
Strain elastography
Shear wave elastography
Summary
MRI is good at detecting high grade, high volume CaP
MRI can influence your biopsy and therapy strategy
TRUS bx or MR guided bx only could miss significant CaP
Experience of the operator plays a major role, standardisation and audit essential
There is a role for fusion biopsy systems and TRUS bx
Biopsy Strategies
MRI can detect high risk CaP but not all
Where do you draw the line for clinically significant CaP?
Do you access to a dedicated uro-radiologist?
Is your finance director friendly?
How much spare theatre capacity do you have?
Any colleagues with interest in taking prostate cancer daignostic pathway further?
Diagnostic pathway strategy
Thank you
Pitfalls MR prostate reporting Panebianco 2015
Diagnostic Bilateral basal hypointense zones (moustache sign) Median posterior hypointense area at the middle third of the gland Transition zone prostate cancer versus BPH foci of stromal hyperplasia Ectopic BPH nodule Granulomatous prostatitis after intravesical instillation of BCG Hypertrophic anterior fibromuscular stroma Periprostatic venous plexus and neurovascular bundle
Staging T3 versus T2 (overlapping with pitfalls in primary diagnosis: granulomatous
prostatitis, periprostatic venous plexus and neurovascular bundle) Bone findings Controversial on lymph nodes
Artifacts Mispositioned endorectal coil Post-biopsy changes Lymphoceles