Abstract
Purpose
To assess the feasibility, safety, and outcomes of an expedited One-Stop prostate cancer (PCa) diagnostic pathway.
Patients and methods
We identified 370 consecutive patients who underwent multiparametric magnetic resonance imaging (mpMRI) and transrectal ultrasound fusion prostate biopsy (MRI/TRUS-PBx) from our institutional review board-approved database. Patients were divided according to diagnostic pathway: One-Stop (n = 74), with mpMRI and same-day PBx, or Standard (n = 296), with mpMRI followed by a second visit for PBx. mpMRIs were performed and interpreted according to Prostate Imaging-Reporting and Data System (PI-RADS v2). Grade group ≥ 2 PCa defined clinically significant PCa (csPCa). Statistical significance was considered when p < 0.05.
Results
Age (66 vs 66 years, p = 0.59) and PSA density (0.1 vs 0.1 ng/mL2, p = 0.26) were not different between One-Stop vs Standard pathway, respectively. One-Stop patients lived further away from the hospital than Standard patients (163 vs 31 km; p < 0.01), and experienced shorter time from mpMRI to PBx (0 vs 7 days; p < 0.01). The number (p = 0.56) and distribution of PI-RADS lesions (p = 0.67) were not different between the groups. All procedures were completed successfully with similar perioperative complications rate (p = 0.24). For patients with PI-RADS 3–5 lesions, the csPCa detection rate (49% vs 41%, p = 0.55) was similar for One-Stop vs Standard, respectively. The negative predictive value of mpMRI (PI-RADS 1–2) for csPCa was 78% for One-Stop vs 83% for Standard (p = 0.99). On multivariate analysis, age, prostate volume and PI-RADS score (p < 0.01), but not diagnostic pathway, predicted csPCa detection.
Conclusion
A One-Stop PCa diagnostic pathway is feasible, safe, and provides similar outcomes in a shorter time compared to the Standard two-visit diagnostic pathway.
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Abbreviations
- ADC:
-
Apparent diffusion coefficient
- AS:
-
Active surveillance
- CI:
-
Confidence interval
- csPCa:
-
Clinically significant prostate cancer
- DCE:
-
Dynamic contrast-enhanced
- DRE:
-
Digital rectal examination
- DWI:
-
Diffusion-weighted images
- IQR:
-
Interquartile range
- ISUP:
-
International Society of Urological Pathology
- mpMRI:
-
Multiparametric magnetic resonance imaging
- MRI/TRUS-PBx:
-
Magnetic resonance imaging transrectal ultrasound fusion-guided prostate biopsy
- NPV:
-
Negative predictive value
- OR:
-
Odds ratio
- PBx:
-
Prostate biopsy
- PCa:
-
Prostate cancer
- PI-RADS v.2:
-
Prostate Imaging-Reporting and Data System Version 2
- PPV:
-
Positive predictive value
- PSA:
-
Prostatic specific antigen
- UTI:
-
Urinary tract infection
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Acknowledgements
This study was funded by the R01 Grant CA205058-01 from the National Institutes of Health/National Cancer Institute (M. C. S, I. S. G. and A. L. D. C. A.) and in part by the Australasian Urological Foundation Scholarship (A. N. A).
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AA, AT, ANA, SP: project development, analysis interpretation, manuscript writing. AS: data collection, manuscript writing and language revision. JC: statistical analysis. AI, TI, AS, CG, LGM: data collection. GEC: data collection and analysis interpretation. MCS, VD, MA, ISG: other (supervision and critical revision).
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The authors declare that they have no conflict of interest. This study was funded by the R01 Grant CA205058-01 from the National Institutes of Health/National Cancer Institute (M. C. S, I. S. G. and A. A.) and in part by the Australasian Urological Foundation Scholarship (A. N. A). Dr. Vinay Duddalwar is a consultant for Intuitive Surgical and Radmetrix, sits on the advisory board for DeepTek, and received grant support from Samsung Healthcare.
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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
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Tafuri, A., Ashrafi, A.N., Palmer, S. et al. One-Stop MRI and MRI/transrectal ultrasound fusion-guided biopsy: an expedited pathway for prostate cancer diagnosis. World J Urol 38, 949–956 (2020). https://doi.org/10.1007/s00345-019-02835-2
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DOI: https://doi.org/10.1007/s00345-019-02835-2