Effect of the PI-RADS score on adverse surgical outcomes in patients with prostate cancer after radical prostatectomy
https://doi.org/10.17650/1726-9776-2024-20-4-24-32
Abstract
Background. Multiparametric magnetic resonance imaging and Prostate Imaging Reporting and Data System (PI-RADS) are widely used to diagnose clinically significant prostate cancer. Meanwhile, PI-RADS diagnostic accuracy varies between 30 % for PI-RADS score 3 to 80 % for PI-RADS score 5. The value of PI-RADS scores in patients already diagnosed with prostate cancer remains unclear.
Aim. To evaluate the impact of PI-RADS score on adverse surgical outcomes: prostate cancer upstaging, increased Gleason score, lymph node metastases, positive surgical margin, and oncological outcomes in patients of the ISUP grade 1 group per the International Society of Urological Pathology (ISUP) scale who underwent radical prostatectomy.
Materials and methods. Forty patients with ISUP grade 1 prostate cancer underwent radical prostatectomy (robotic or laparoscopic). All patients underwent diagnostic multiparametric magnetic resonance imaging with PI-PADS score v2 (v2.1) prior to radical prostatectomy. PI-RADS 3 was determined in 14 (35 %), PI-RADS 4 – in 10 (25 %) and PI-RADS 5 – in 16 (40 %) patients, respectively. The age of patients was 62.7 ± 6.6 years. Stage cT2a was diagnosed in 19 (47.5 %), cT2b – in 5 (12.5 %), cT2c – in 11 (27.5 %), cT3a – in 5 (12.5 %) patients, respectively. Pelvic lymph node dissection was performed in 23 (57.5 %) cases. The median follow-up was 12.6 months.
Results. Upstaging events to pT3a occurred in 2 (15.2 %) patients with PI-RADS 3 lesions, in 5 (31.3 %) patients with PI-RADS 5 lesions; upstaging events to pT3b occurred in 1 (10 %) patient with PI-RADS 4 lesions, and in 1 (6.25 %) patient with PI-RADS 5 lesions. Increased Gleason score (GS) was observed in 22 (55 %) patients: GS increase ≥2 was diagnosed in 8 (57.1 %) patients with PI-RADS 3 lesions, in 3 (30 %) patients with PI-RADS 4 lesions, in 11 (68.7 %) patients with PI-RADS 5 lesions, respectively. Lymph node metastases were observed only in 1 (4.3 %) patient with PI-RADS 5 lesions. Positive surgical margin (>3 mm) was observed in 2 (12.4 %) patients with PI-RADS 5 lesions. Biochemical recurrence occurred in 1 (2.5 %) patient with PI-RADS 3 lesions. One-year biochemical recurrence-free survival was 97.5 %.
Conclusion. Increased PI-RADS score from 3 to 5 is accompanied by increased frequency of prostate cancer upstaging and Gleason score increase in patients with ISUP grade 1 prostate cancer. PI-RADS scores 3–5 can be important in selecting patients for nerve-sparing prostatectomy, pelvic lymph node dissection, and play a part in prediction of biochemical recurrence and lymph node metastasis.
About the Authors
A. M. PopovRussian Federation
15 Marshala Timoshenko St., Moscow 121359
Competing Interests:
None
E. V. Anikanova
Russian Federation
Ekaterina V. Anikanova.
15 Marshala Timoshenko St., Moscow 121359
Competing Interests:
None
O. V. Kryuchkova
Russian Federation
15 Marshala Timoshenko St., Moscow 121359
Competing Interests:
None
A. A. Sokolov
Russian Federation
15 Marshala Timoshenko St., Moscow 121359
Competing Interests:
None
E. F. Abdryakhimov
Russian Federation
15 Marshala Timoshenko St., Moscow 121359
Competing Interests:
None
E. V. Zarya
Russian Federation
15 Marshala Timoshenko St., Moscow 121359
Competing Interests:
None
References
1. Thompson J.E., Moses D., Shnier R. et al. Multiparametric magnetic resonance imaging guided diagnostic biopsy detects significant prostate cancer and could reduce unnecessary biopsies and over detection: a prospective study. J Urol 2014;192:67. DOI: 10.1016/j.juro.2014.08.118
2. Tan N., Lin W.C., Khoshnoodi P. et al. In-bore 3-T MR-guided transrectal targeted prostate biopsy: Prostate Imaging Reporting and Data System Version 2-based diagnostic performance for detection of prostate cancer. Radiology 2017;283:130–9. DOI: 10.1148/radiol.2016152827
3. Turkbey B., Rosenkrantz A.B., Haider M.A. 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(3):340–51. DOI: 10.1016/j.eururo.2019.02.033
4. Sonn G.A., Fan R.E., Ghanouni P. et al. Prostate magnetic resonance imaging interpretation varies substantially across radiologists. Eur Urol Focus 2019;5:592. DOI: 10.1016/j.euf.2017.11.010
5. Benjamin P., Kristian D.S., Molly P. et al. MRI PI-RADS scores are associated with prostate cancer upstaging on surgical pathology. Prostate 2022;82(3):352–8. DOI: 10.1002/pros.24280
6. Sung K.H., Sang H.S., Hak J.K. et al. Temporal changes of PIRADS scoring by radiologists and correlation to radical prostatectomy pathological outcomes. Prostate Int 2022;10(4):188–93. DOI: 10.1016/j.prnil.2022.07.001
7. Sokolov E.A., Veliev E.I., Veliev R.A. et al. Oncological results of radical prostatectomy depending on the data of multiparametric magnetic resonance imaging and patient selection for nerve-sparing technique. Onkourologiya = Cancer Urology 2020;16(2):74–81. (In Russ.). DOI: 10.17650/1726-9776-2020-16-2-74-81
8. O’Connor L., Wang A., Walker S.M. et al. Use of multiparametric magnetic resonance imaging (mpMRI) in localized prostate cancer. Expert Rev Med Devices 2020;17(5):435–42. DOI: 10.1080/17434440.2020.1755257
9. Somford D.M., Hamoen E.H., Futterer J.J. et al. The predictive value of endorectal 3 Tesla multiparametric magnetic resonance imaging for extraprostatic extension in patients with low, intermediate and high risk prostate cancer. J Urol 2013;190:1728–34. DOI: 10.1016/j.juro.2013.05.021
10. Izak F., Amirali S., Neil M. et al. PI-RADS version 2 category on 3 Tesla multiparametric prostate magnetic resonance imaging predicts oncologic outcomes in Gleason 3+4 prostate cancer on biopsy. J Urol 2019;201(1):91–7. DOI: 10.1016/j.juro.2018.08.043
11. Hassan O., Han M., Zhou A. et al. Incidence of extraprostatic extension at radical prostatectomy with pure Gleason score 3 + 3 = 6 (Grade Group 1) cancer: implications for whether Gleason score 6 prostate cancer should be renamed “not cancer” and for selection criteria for active surveillance. J Urol 2018;199(6):1482–7. DOI: 10.1016/j.juro.2017.11.067
12. Yossepowitch O., Briganti A., Eastham J.A. et al. Positive surgical margins after radical prostatectomy: a systematic review and contemporary update. Eur Urol 2014; 65:303–13. DOI: 10.1016/j.eururo.2013.07.039
13. Preston M.A., Blute M.L. Positive surgical margins after radical prostatectomy: does it matter? Eur Urol 2014;65:314–31. DOI: 10.1016/j.eururo.2013.08.037
14. Abdollah F., Abdo A., Sun M. et al. Pelvic lymph node dissection for prostate cancer: adherence and accuracy of the recent guidelines. Int J Urol 2013;20:405–10. DOI: 10.1111/j.1442-2042.2012.03171.x
15. Huang C., Song G., Wang H. et al. Multiparametric magnetic resonance imaging-based nomogram for predicting prostate cancer and clinically significant prostate cancer in men undergoing repeat prostate biopsy. Biomed Res Int 2018:6368309. DOI: 10.1155/2018/6368309
16. Cookson M.S., Aus G., Burnett A.L. et al. Variation in the definition of biochemical recurrence in patients treated for localized prostate cancer: the American Urological Association Prostate Guidelines for Localized Prostate Cancer Update Panel report and recommendations for a standard in the reporting of surgical outcomes. J Urol 2007;177:540–5. DOI: 10.1016/j.juro.2006.10.097
17. Rajwa P., Mori K., Huebner N.A. et al. The prognostic association of prostate MRI PI-RADS v2 assessment category and risk of biochemical recurrence after definitive local therapy for prostate cancer: a systematic review and meta-analysis. J Urol 2021;206(3):507–16. DOI: 10.1097/JU.0000000000001821
Review
For citations:
Popov A.M., Anikanova E.V., Kryuchkova O.V., Sokolov A.A., Abdryakhimov E.F., Zarya E.V. Effect of the PI-RADS score on adverse surgical outcomes in patients with prostate cancer after radical prostatectomy. Cancer Urology. 2024;20(4):24-32. (In Russ.) https://doi.org/10.17650/1726-9776-2024-20-4-24-32