Applicability of PIRADs 2.1 scoring system to screen Prostate Cancer in a Ugandan population, a cross-sectional study.
DOI:
https://doi.org/10.51168/c3q1rs78Keywords:
Prostate, cancer, Magnetic Resonance Imaging (MRI), Sub-Saharan Africa, BI-Parametric Magnetic Resonance Imaging (MRI), Prostate Imaging Reporting and Data System (PIRADS), Prostate Cancer, UgandaAbstract
Background/Objectives:
Prostate Cancer (PCa) is highly prevalent in Africa. The Prostate Imaging Reporting and Data System (PIRADS) is used for detecting, staging, standardizing the acquisition, and reporting of BI-Parametric Magnetic Resonance Imaging (MRI) (Bp-MRI). The PIRADS is a “living” document and, through research, should be tested and validated for different healthcare settings. There is hardly any literature on the applicability and accuracy of the PIRADS 2.1 to screen for PCa in sub-Saharan Africa. The study sought to assess the applicability of the PIRADS 2.1 scoring system to screen PCa in sub-Saharan Africa.
Methods:
A retrospective review of imaging requisitions was done, including Bp-MRI, MRI reports, and histology reports, including the Gleason score, at an imaging institution in Uganda. The study assessed the ability of PIRADS alone, PIRADS and prostate specific antigen density (PSAD), PIRADS and Apparent Diffusion Coefficient (ADC), and PIRADS, PSAD, and ADC-combination to discriminate a positive histological prostate case. The study used the Area Under the Curve to determine the ability of PIRADS 2.1 to discriminate PCa.
Results:
The study reviewed 234 patient records, and of these, 99 were aged 65-74 years, and 48.7% were PCa histology-confirmed cases. PIRADS alone had an AUC 0.70, a combination of PIRADS V2.1 and PSAD had an AUC score 0.73, while a combination of PIRADS V2.1, PSAD, and ADC had an AUC 0.72.
Conclusions:
The accuracy of PIRADS for PCa discrimination is acceptable with an AUC 70%. Predominantly peripheral zone location, together with the low Gleason score and the background changes of chronic prostatitis, may account for the low PIRADS cancer prediction.
References
1. Wang, L., Lu, B., He, M., Wang, Y., Wang, Z., & Du, L. (2022). Prostate cancer incidence and mortality: global status and temporal trends in 89 countries from 2000 to 2019. Frontiers in Public Health, 10, 811044.
2. Okuku, F., Orem, J., Holoya, G., De Boer, C., Thompson, C. L., & Cooney, M. M. (2016). Prostate cancer burden at the Uganda cancer institute. Journal of global oncology, 2(4), 181–185.
3. Stenman, U.-H., Leinonen, J., Alfthan, H., Rannikko, S., Tuhkanen, K., & Alfthan, O. (1991). A complex between prostate-specific antigen and α1-antichymotrypsin is the major form of prostate-specific antigen in serum of patients with prostatic cancer: assay of the complex improves clinical sensitivity for cancer. Cancer research, 51(1), 222–226.
4. Murphy, G., Haider, M., Ghai, S., & Sreeharsha, B. (2013). The expanding role of MRI in prostate cancer. AJR Am J Roentgenol, 201(6), 1229–38.
5. Pesapane, F., Acquasanta, M., Meo, R. D., Agazzi, G. M., Tantrige, P., Codari, M., … Sardanelli, F. (2021). Comparison of sensitivity and specificity of biparametric versus multiparametric prostate mri in the detection of prostate cancer in 431 men with elevated prostate-specific antigen levels. Diagnostics, 11(7), 1223.
6. Bass, E. J., Pantovic, A., Connor, M., Gabe, R., Padhani, A. R., Rockall, A., … Ahmed, H. U. (2021). A systematic review and meta-analysis of the diagnostic accuracy of biparametric prostate MRI for prostate cancer in men at risk. Prostate Cancer and Prostatic Diseases, 24(3), 596–611.
7. Weinreb, J. C., Barentsz, J. O., Choyke, P. L., Cornud, F., Haider, M. A., Macura, K. J., … Tempany, C. M. (2016). PI-RADS prostate imaging–reporting and data system: 2015, version 2. European urology, 69(1), 16–40.
8. Park, K. J., Choi, S. H., Kim, M., Kim, J. K., & Jeong, I. G. (2021). Performance of Prostate Imaging Reporting and Data System Version 2.1 for Diagnosis of Prostate Cancer: A Systematic Review and Meta-Analysis. Journal of Magnetic Resonance Imaging, 54(1), 103–112.
9. Distler, F. A., Radtke, J. P., Bonekamp, D., Kesch, C., Schlemmer, H.-P., Wieczorek, K., … Hadaschik, B. A. (2017). The value of PSA density in combination with PI-RADSTM for the accuracy of prostate cancer prediction. The Journal of urology, 198(3), 575–582.
10. Jordan, E. J., Fiske, C., Zagoria, R., & Westphalen, A. C. (2018). PI-RADS v2 and ADC values: is there room for improvement? Abdominal Radiology, 43(11), 3109–3116.
11. Walker, S. M., Mehralivand, S., Harmon, S. A., Sanford, T., Merino, M. J., Wood, B. J., … Turkbey, B. (2020). Prospective evaluation of PI-RADS version 2.1 for prostate cancer detection. AJR. American journal of roentgenology, 1.
12. Danneman, D., Drevin, L., Robinson, D., Stattin, P., & Egevad, L. (2015). Gleason inflation 1998–2011: a registry study of 97 168 men. BJU International, 115(2), 248–255. https://doi.org/10.1111/bju.12671
13. Rawla, P. (2019). Epidemiology of prostate cancer. World journal of oncology, 10(2), 63.
14. Vickers, A. J., Sjoberg, D. D., Ulmert, D., Vertosick, E., Roobol, M. J., Thompson, I., … Scardino, P. T. (2014). Empirical estimates of prostate cancer overdiagnosis by age and prostate-specific antigen. BMC medicine, 12(1), 1–7.
15. Schröder, F. H., Hugosson, J., Carlsson, S., Tammela, T., Määttänen, L., Auvinen, A., … Roobol, M. J. (2012). Screening for prostate cancer decreases the risk of developing metastatic disease: findings from the European Randomized Study of Screening for Prostate Cancer (ERSPC). European urology, 62(5), 745–752.
16. ACR. (2019). Prostate Imaging – Reporting and Data System Version 2.1. Retrieved from https://www.acr.org/-/media/ACR/Files/RADS/Pi-RADS/PIRADS-V2-1.pdf
17. Yu, X., Liu, R., Song, L., Gao, W., Wang, X., & Zhang, Y. (2023). Differences in the pathogenetic characteristics of prostate cancer in the transitional and peripheral zones and the possible molecular biological mechanisms. Frontiers in Oncology, 13, 1165732.
18. Danneman, D., Drevin, L., Robinson, D., Stattin, P., & Egevad, L. (2015). Gleason inflation 1998–2011: a registry study of 97 168 men. BJU international, 115(2), 248–255.
19. Manetta, R., Palumbo, P., Gianneramo, C., Bruno, F., Arrigoni, F., Natella, R., … Di Cesare, E. (2019). Correlation between ADC values and Gleason score in evaluation of prostate cancer: multicentre experience and review of the literature. Gland surgery, 8(Suppl 3), S216.
20. Nagarajan, R., Margolis, D., Raman, S., Sheng, K., King, C., Reiter, R., & Thomas, M. A. (2012). Correlation of Gleason scores with diffusion-weighted imaging findings of prostate cancer. Advances in urology, 2012.
21. Anwar, S. S. M., Anwar Khan, Z., Shoaib Hamid, R., Haroon, F., Sayani, R., Beg, M., & Khattak, Y. J. (2014). Assessment of apparent diffusion coefficient values as predictor of aggressiveness in peripheral zone prostate cancer: comparison with Gleason score. International Scholarly Research Notices, 2014.
22. Fine, S. W., Al-Ahmadie, H. A., Vertosick, E., Vickers, A. J., Chen, Y.-B., Gopalan, A., … Reuter, V. E. (2022). Impact of Zone of Origin in Anterior Dominant Prostate Cancer: Long-Term Biochemical Recurrence-Free Survival in an Anatomically Well-Characterized Cohort. Urology Practice, 9(5), 459–465. https://doi.org/10.1097/UPJ.0000000000000322
23. Kasel-Seibert, M., Lehmann, T., Aschenbach, R., Guettler, F. V., Abubrig, M., Grimm, M.-O., … Franiel, T. (2016). Assessment of PI-RADS v2 for the detection of prostate cancer. European journal of radiology, 85(4), 726–731.
24. Cai, G.-H., Yang, Q.-H., Chen, W.-B., Liu, Q.-Y., Zeng, Y.-R., & Zeng, Y.-J. (2021). Diagnostic Performance of PI-RADS v2, Proposed Adjusted PI-RADS v2 and Biparametric Magnetic Resonance Imaging for Prostate Cancer Detection: A Preliminary Study. Current Oncology, 28(3), 1823–1834.
25. Hötker, A. M., Blüthgen, C., Rupp, N. J., Schneider, A. F., Eberli, D., & Donati, O. F. (2020). Comparison of the PI-RADS 2.1 scoring system to PI-RADS 2.0: Impact on diagnostic accuracy and inter-reader agreement. Plos one, 15(10), e0239975.
26. Nadler, R. B., Collins, M. M., Propert, K. J., Mikolajczyk, S. D., Knauss, J. S., Landis, J. R., … Network, C. P. C. R. (2006). Prostate-specific antigen test in diagnostic evaluation of chronic prostatitis/chronic pelvic pain syndrome. Urology, 67(2), 337–342.
27. Stevens, E., Truong, M., Bullen, J. A., Ward, R. D., Purysko, A. S., & Klein, E. A. (2020). Clinical utility of PSAD combined with PI-RADS category for the detection of clinically significant prostate cancer. In Urologic Oncology: Seminars and Original Investigations (Vol. 38, pp. 846-e9). Elsevier.
28. Lin, W. C., Westphalen, A. C., Silva, G. E., Chodraui Filho, S., Reis, R. B. dos, & Muglia, V. F. (2016). Comparison of PI-RADS 2, ADC histogram-derived parameters, and their combination for the diagnosis of peripheral zone prostate cancer. Abdominal Radiology, 41(11), 2209–2217.
29. Yu, J., Fulcher, A. S., Turner, M. A., Cockrell, C. H., Cote, E. P., & Wallace, T. J. (2014). Prostate cancer and its mimics at multiparametric prostate MRI. The British journal of radiology, 87(1037), 20130659.
30. Wen, J., Liu, W., Shen, X., & Hu, W. (2024). PI-RADS v2. 1 and PSAD for the prediction of clinically significant prostate cancer among patients with PSA levels of 4–10 ng/ml. Scientific Reports, 14(1), 6570.
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