Abstract
Purpose
To investigate the effects of various prostate biopsy protocols with reduced cores on the detection of clinically significant prostate cancer (csPCa) in individuals with MRI-visible lesions (Prostate Imaging Reporting and Data System ≥ 3).
Methods
A total of 464 patients with MRI-visible lesions were recruited. All patients underwent two or more targeted biopsies (TB) and systematic biopsies (SB). Several hypothetical biopsy schemes were set-up: TB alone, TB+ipsilateral SB, TB+contralateral SB, TB+SB of the targeted sector (TB+t-SB), and TB+SB of the non-targeted sector (TB+n-SB). A subgroup analysis of patients with multiple MRI-visible lesions was performed. The standard of reference was defined as TB+SB. McNemar test was used to compare csPCa detection rates between various sampling schemes.
Results
The detection rates for prostate cancer and csPCa were 72.8% (338 of 464) and 62.1% (288 of 464), respectively. There were 8.0%, 0.3%, 6.3%, 1.0%, and 4.5% cases in which TB alone, TB+ipsilateral SB, TB+contralateral SB, TB+t-SB, and TB+n-SB would have missed csPCa, respectively. All hypothetical schemes, with the exception of TB+contralateral SB (p = 0.063), significantly outperformed TB alone in terms of csPCa detection (p < 0.05). As for the multi-focus cohort, which included 48 cases, none of the non-index lesions had a higher Gleason grade than the index lesions within the same patients.
Conclusion
TB+ipsilateral SB might be the optimal biopsy scheme for detecting csPCa. As for the multi-focus cohort, the biopsy of the non-index lesions provided limited pathological information.
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Abbreviations
- PCa:
-
Prostate cancer
- csPCa:
-
Clinically significant prostate cancer
- mpMRI:
-
Multiparametric magnetic resonance imaging
- US:
-
Ultrasound
- TB:
-
Targeted biopsy
- PI-RADS v2.1:
-
Prostate Imaging Reporting and Data System version 2.1
- SB:
-
Systematic biopsy
- ciPCa:
-
Clinically insignificant prostate cancer
- TS:
-
Target saturation
- ipsi-SB:
-
Ipsilateral systematic biopsy
- n-SB:
-
Systematic biopsy of the non-targeted sector
- contra-SB:
-
Contralateral systematic biopsy
- t-SB:
-
Systematic biopsy of the targeted sector
- IL:
-
Index lesion
- PSA:
-
Prostate-specific antigen
- PSAD:
-
Prostate-specific antigen density
- PV:
-
Prostate volume
- DRE:
-
Digital rectal examination
- GS:
-
Gleason score
- PZ:
-
Peripheral zone
- TZ:
-
Transitional zone
- nIL:
-
Non-index lesion
- GG:
-
Grade group
- IQR:
-
Interquartile range
- NPV:
-
Negative predictive value
- ROC:
-
Receiver operating characteristic curve
- AUC:
-
Area under the receiver operating characteristic curve
- CI:
-
Confidence interval
References
Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin 2021;71:209–49. https://doi.org/10.3322/caac.21660.
Padhani AR, Weinreb J, Rosenkrantz AB, Villeirs G, Turkbey B, Barentsz J. Prostate Imaging-Reporting and Data System Steering Committee: PI-RADS v2 Status Update and Future Directions. Eur Urol 2019;75:385–96. https://doi.org/10.1016/j.eururo.2018.05.035.
Taneja SS. Comparison of MR/ultrasound fusion-guided biopsy with ultrasound-guided biopsy for the diagnosis of prostate cancer. J Urol 2015;194:112–5. https://doi.org/10.1016/j.juro.2015.04.062.
N. Mottet van den B, E. Briers PC, J. Grummet AMHMDSSFSG, T.H. van der Kwast HG van der PTBLMDM, D. Tilki TWOR, Guidelines Associates: T. Van den Broeck MC, et al. EAU - EANM - ESTRO - ESUR - SIOG Guidelines on Prostate Cancer 2019. Eur Assoc Urol Guidel 2019 2019;53:1–161.
Mri P. Prostate MRI, with or without MRI-targeted biopsy, and systematic biopsy for detecting prostate cancer (Review) 2019. https://doi.org/10.1002/14651858.CD012663.pub2.www.cochranelibrary.com.
Goldberg H, Ahmad AE, Chandrasekar T, Klotz L, Emberton M, Haider MA, et al. Comparison of Magnetic Resonance Imaging and Transrectal Ultrasound Informed Prostate Biopsy for Prostate Cancer Diagnosis in Biopsy Naïve Men: A Systematic Review and Meta-Analysis. J Urol 2020;203:1085–93. https://doi.org/10.1097/ju.0000000000000595.
Kasivisvanathan V, Rannikko AS, Borghi M, Panebianco V, Mynderse LA, Vaarala MH, et al. MRI-Targeted or Standard Biopsy for Prostate-Cancer Diagnosis. N Engl J Med 2018. https://doi.org/10.1056/nejmoa1801993.
van der Leest M, Cornel E, Israël B, Hendriks R, Padhani AR, Hoogenboom M, et al. Head-to-head Comparison of Transrectal Ultrasound-guided Prostate Biopsy Versus Multiparametric Prostate Resonance Imaging with Subsequent Magnetic Resonance-guided Biopsy in Biopsy-naive Men with Elevated Prostate-specific Antigen: A Large Prospective Mu. Eur Urol 2019;75:570–8. https://doi.org/10.1016/j.eururo.2018.11.023.
Stabile A, Giganti F, Rosenkrantz AB, Taneja SS, Villeirs G, Gill IS, et al. Multiparametric MRI for prostate cancer diagnosis: current status and future directions. Nat Rev Urol 2020;17:41–61. https://doi.org/10.1038/s41585-019-0212-4.
Tschirdewahn S, Wiesenfarth M, Bonekamp D, Püllen L, Reis H, Panic A, et al. Detection of Significant Prostate Cancer Using Target Saturation in Transperineal Magnetic Resonance Imaging/Transrectal Ultrasonography–fusion Biopsy. Eur Urol Focus 2020:1–8. https://doi.org/10.1016/j.euf.2020.06.020.
Dell P, Stabile A, Soligo M, Brembilla G, Esposito A, Gandaglia G, et al. There Is No Way to Avoid Systematic Prostate Biopsies in Addition to Multiparametric Magnetic Resonance Imaging Targeted Biopsies 2019:1–7. https://doi.org/10.1016/j.euo.2019.03.002.
D YFM, Xi Y, D NPM, D SWM, Mpas BH, D KGM, et al. Optimal sampling scheme in men with abnormal multiparametric MRI undergoing MRI-TRUS fusion prostate biopsy. Urol Oncol Semin Orig Investig 2018;000:1–6. https://doi.org/10.1016/j.urolonc.2018.10.009.
Bryk DJ, Llukani E, Taneja SS, Rosenkrantz AB, Huang WC, Lepor H. The Role of Ipsilateral and Contralateral Transrectal Ultrasound-guided Systematic Prostate Biopsy in Men With Unilateral Magnetic Resonance Imaging Lesion Undergoing Magnetic Resonance Imaging-ultrasound Fusion-targeted Prostate Biopsy. Urology 2017;102:178–82. https://doi.org/10.1016/j.urology.2016.11.017.
Shen WW, Cui LG, Ran WQ, Sun Y, Jiang J, Pei XL, et al. Targeted Biopsy With Reduced Number of Cores: Optimal Sampling Scheme in Patients Undergoing Magnetic Resonance Imaging/Transrectal Ultrasound Fusion Prostate Biopsy. Ultrasound Med Biol 2020;00:1–11. https://doi.org/10.1016/j.ultrasmedbio.2020.01.017.
Liu H, Ruan M, Wang H, Wang H, Li X, Song G. Can fewer transperineal systematic biopsy cores have the same prostate cancer detection rate as of magnetic resonance imaging / ultrasound fusion biopsy ? Prostate Cancer Prostatic Dis 2020. https://doi.org/10.1038/s41391-020-0260-0.
Turkbey B, Rosenkrantz AB, Haider MA, Padhani AR, Villeirs G, Macura KJ, et al. Prostate Imaging Reporting and Data System Version 2.1: 2019 Update of Prostate Imaging Reporting and Data System Version 2. Eur Urol 2019;76:340–51. https://doi.org/10.1016/j.eururo.2019.02.033.
Barentsz JO, Weinreb JC, Verma S, Thoeny HC, Tempany CM, Shtern F, et al. Synopsis of the PI-RADS v2 Guidelines for Multiparametric Prostate Magnetic Resonance Imaging and Recommendations for Use. Eur Urol 2016;69:41–9. https://doi.org/10.1016/j.eururo.2015.08.038.
Song G, Ruan M, Wang H, Fan Y, He Q, Lin Z, et al. How Many Targeted Biopsy Cores are Needed for Clinically Significant Prostate Cancer Detection during Transperineal Magnetic Resonance Imaging Ultrasound Fusion Biopsy? J Urol 2020. https://doi.org/10.1097/ju.0000000000001302.
Epstein JI, Egevad L, Amin MB, Delahunt B, Srigley JR, Humphrey PA. The 2014 international society of urological pathology (ISUP) consensus conference on gleason grading of prostatic carcinoma definition of grading patterns and proposal for a new grading system. Am J Surg Pathol 2016;40:244–52. https://doi.org/10.1097/PAS.0000000000000530.
Kasivisvanathan V, Rannikko AS, Borghi M, Panebianco V, Mynderse LA, Vaarala MH, et al. MRI-targeted or standard biopsy for prostate-cancer diagnosis. N Engl J Med 2018;378:1767–77. https://doi.org/10.1056/NEJMoa1801993.
Andreoiu M, Cheng L. Multifocal prostate cancer: biologic, prognostic, and therapeutic implications. Hum Pathol 2010;41:781–93. https://doi.org/10.1016/j.humpath.2010.02.011.
Karavitakis M, Winkler M, Abel P, Livni N, Beckley I, Ahmed HU. Histological characteristics of the index lesion in whole-mount radical prostatectomy specimens: Implications for focal therapy. Prostate Cancer Prostatic Dis 2011;14:46–52. https://doi.org/10.1038/pcan.2010.16.
Stamatakis L, Siddiqui MM, Nix JW, Logan J, Rais-Bahrami S, Walton-Diaz A, et al. Accuracy of multiparametric magnetic resonance imaging in confirming eligibility for active surveillance for men with prostate cancer. Cancer 2013;119:3359–66. https://doi.org/10.1002/cncr.28216.
Johnson DC, Raman SS, Mirak SA, Kwan L, Bajgiran AM, Hsu W, et al. Detection of Individual Prostate Cancer Foci via Multiparametric Magnetic Resonance Imaging. Eur Urol 2019;75:712–20. https://doi.org/10.1016/j.eururo.2018.11.031.
Patel N, Halpern JA, Kasabwala K, Cricco-lizza E, Herman M, Margolis D, et al. Multiple regions of interest on multi-parametric magnetic resonance imaging are not associated with increased detection of clinically significant prostate cancer on fusion biopsy. J Urol 2018. https://doi.org/10.1016/j.juro.2018.03.002.
Stabile A, Barletta F, Motterle G, Pellegrino F, Sorce G, Mazzone E, et al. Optimizing prostate-targeted biopsy schemes in men with multiple mpMRI visible lesions: should we target all suspicious areas? Results of a two institution series. Prostate Cancer Prostatic Dis 2021. https://doi.org/10.1038/s41391-021-00371-y.
Funding
This study was supported by funding from Capital’s Funds for Health Improvement and Research (Grant No. 2022-3-40714).
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All authors contributed to the study conception and design. Material preparation, data collection, and analysis were performed by MR, HW, XL, and GS. The first draft of the manuscript was written by MR and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript. Conceptualization: GS and MR; Methodology: GS and MR; Formal analysis and investigation: MR and HW, XL; Writing—original draft preparation: MR; Writing—review and editing: GS; Funding acquisition: GS; Resources: GS and HW; Supervision: GS.
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Ruan, M., Wang, H., Li, X. et al. Novel sampling scheme with reduced cores in men with multiparametric MRI-visible lesions undergoing prostate biopsy. Abdom Radiol 48, 2139–2147 (2023). https://doi.org/10.1007/s00261-023-03894-1
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DOI: https://doi.org/10.1007/s00261-023-03894-1