“…MRI-guided biopsy more accurately characterizes whole-organ pathology than conventional US-guided biopsy 7–9 . In previous studies, we and others have found that MRI-guided biopsy including target and template samples 10 , helps to detect clinically significant disease (csCaP) in men being screened for AS 11,12 .…”
Purpose
To determine rate of upgrading to Gleason score (GS) ≥ 4+3, using targeted biopsy for diagnosis and monitoring, in men undergoing active surveillance (AS) of prostate cancer (CaP).
Materials and Methods
Subjects were all 259 men (196 with GS 3+3 and 63 with GS 3+4) who were diagnosed by MRI/US fusion-guided biopsy (2009–2015) and who underwent subsequent fusion biopsy for as long as 4 years of AS. Primary endpoint was discovery of GS ≥ 4+3 CaP. Follow-up biopsies included targeting of positive sites, which were tracked in an Artemis device. Kaplan-Meier curves were generated to determine rates of upgrading, stratified by initial GS and PSA density.
Results
Based on a Cox proportional hazard model, men with GS 3+4 were 4.65 more likely to have upgrading than men with initial GS 3+3 (3yr, p < 0.01). 63% of men with GS 3+4 had upgraded by the third surveillance year, compared with 18.0% of men starting with GS 3+3 (p < 0.01). 97% of all upgrades (32/33) occurred within an MRI-visible or a tracked site of tumor, rather than a previously-negative systematic site. Independent predictors of upgrading were GS 3+4, PSA density ≥ 0.15 ng/ml/cm3, and a grade 5 lesion on MRI. The incidence-rate ratio of upgrading (GS 3+4 vs. GS 3+3) was 4.25 per year of patient follow-up (p < 0.01).
Conclusions
During AS of CaP, targeting of tracked tumor foci by MRI/US fusion biopsy allows heightened detection of GS ≥ 4+3 cancers. Baseline variables directly related to important upgrading and warranting increased vigilance include GS 3+4, PSA density ≥ 0.15, and grade 5 lesions on MRI.
“…MRI-guided biopsy more accurately characterizes whole-organ pathology than conventional US-guided biopsy 7–9 . In previous studies, we and others have found that MRI-guided biopsy including target and template samples 10 , helps to detect clinically significant disease (csCaP) in men being screened for AS 11,12 .…”
Purpose
To determine rate of upgrading to Gleason score (GS) ≥ 4+3, using targeted biopsy for diagnosis and monitoring, in men undergoing active surveillance (AS) of prostate cancer (CaP).
Materials and Methods
Subjects were all 259 men (196 with GS 3+3 and 63 with GS 3+4) who were diagnosed by MRI/US fusion-guided biopsy (2009–2015) and who underwent subsequent fusion biopsy for as long as 4 years of AS. Primary endpoint was discovery of GS ≥ 4+3 CaP. Follow-up biopsies included targeting of positive sites, which were tracked in an Artemis device. Kaplan-Meier curves were generated to determine rates of upgrading, stratified by initial GS and PSA density.
Results
Based on a Cox proportional hazard model, men with GS 3+4 were 4.65 more likely to have upgrading than men with initial GS 3+3 (3yr, p < 0.01). 63% of men with GS 3+4 had upgraded by the third surveillance year, compared with 18.0% of men starting with GS 3+3 (p < 0.01). 97% of all upgrades (32/33) occurred within an MRI-visible or a tracked site of tumor, rather than a previously-negative systematic site. Independent predictors of upgrading were GS 3+4, PSA density ≥ 0.15 ng/ml/cm3, and a grade 5 lesion on MRI. The incidence-rate ratio of upgrading (GS 3+4 vs. GS 3+3) was 4.25 per year of patient follow-up (p < 0.01).
Conclusions
During AS of CaP, targeting of tracked tumor foci by MRI/US fusion biopsy allows heightened detection of GS ≥ 4+3 cancers. Baseline variables directly related to important upgrading and warranting increased vigilance include GS 3+4, PSA density ≥ 0.15, and grade 5 lesions on MRI.
“…Han et al showed that using ultrasound alone, even skilled and experienced urologists are often unable to match their planned core location to the actual site to be sampled within the prostate (14). With the advent of image-fusion devices, recording and later resampling of specific sites containing tumor foci became possible (5,15,16). Some tumors are found outside of MRI-visible lesions or ROIs (12); they can still be tracked.…”
The tracking function of magnetic resonance imaging-ultrasound fusion biopsy warrants further study. When specific sites are resampled in men undergoing active surveillance of prostate cancer, upgrading is detected more often than by nontracking biopsy.
“…Multiparametric MRI (mpMRI) is established in the UK as a useful tool to aid prostate cancer diagnosis, and it is recommended in the 2014 NICE guidelines for the assessment of men, both early in surveillance, and during follow‐up . The exact role of mpMRI in AS is under discussion, including the possibility that it can be used to avoid repeat biopsies in some men . Trials with long‐term follow‐up incorporating mpMRI within AS protocols, such as the SPCG17: Prostate Cancer Active Surveillance Trigger Trial (clinicaltrials.gov identifier NCT02914873), are ongoing.…”
Objectives
To develop a consensus statement on current best practice of active surveillance (AS) in the UK, informed by patients and clinical experts.
Subjects and Methods
A consensus statement was drafted on the basis of three sources of data: systematic literature search of national and international guidelines; data arising from a Freedom of Information Act request to UK urology departments regarding their current practice of AS; and survey and interview responses from men with localized prostate cancer regarding their experiences and views of AS. The Prostate Cancer UK Expert Reference Group (ERG) on AS was then convened to discuss and refine the statement.
Results
Guidelines and protocols for AS varied significantly in terms of risk stratification, criteria for offering AS, and protocols for AS between and within countries. Patients and healthcare professionals identified clinical, emotional and process needs for AS to be effective. Men with prostate cancer wanted more information and psychological support at the time of discussing AS with the treating team and in the first 2 years of AS, and a named healthcare professional to discuss any questions or concerns they had. The ERG agreed 30 consensus statements regarding best practice for AS. Statements were grouped under headings: ‘Inclusion/Exclusion Criteria’; ‘AS follow‐up protocol’ and ‘When to stop AS’.
Conclusion
Significant variation currently exists in the practice of AS in the UK and internationally. Men have clear views on the level of involvement in treatment decisions and support from their treating professionals when receiving AS. The Prostate Cancer UK AS ERG has developed a set of consensus statements for best practice in AS. Evidence for best practice in AS, and the use of multiparametric magnetic resonance imaging in AS, is still evolving, and further studies are needed to determine how to optimize AS outcomes.
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