A risk grouping algorithm for predicting factors of persistently elevated prostate‐specific antigen in patients following robot‐assisted radical prostatectomy. Issue 10 (22nd June 2021)

• Record Type: Journal Article
• Authors: Micoogullari, Uygar; Cakici, Mehmet Caglar; Kisa, Erdem; Canda, Abdullah Erdem; Kilic, Furkan Umut; Ardicoglu, Arslan; Altinova, Serkan; Atmaca, Ali Fuat; Akbulut, Ziya; Balbay, Mevlana Derya
• Is Part Of: International journal of clinical practice. Volume 75:Issue 10(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-06-22
• Subjects: BCR free survival -- persistent PSA -- prostate Cancer -- prostate specific antigen -- risk grouping algorithm -- robot assisted radical prostatectomy; Clinical medicine -- Periodicals; Medicine -- Periodicals; 610.5
• DOI: 10.1111/ijcp.14495
• Languages: English
• ISSNs: 1368-5031

Abstract

Abstract: Objective: After radical prostatectomy, prostate‐specific antigen(PSA) value measuring ≥0.1 ng/mL is defined as persistent PSA(pPSA) and in many studies, it was found to be associated with aggressive disease and poor prognosis. Our aim in this study is to point out the pathological and clinical factors affecting pPSA among the patients who underwent robot‐assisted radical prostatectomy(RARP) in an experienced academic centre and to make a useful risk grouping algorithm that can predict pPSA value based on operative data. Methods: We examined records of 1273 patients who underwent RARP retrospectively. Preoperative, operative and postoperative data were collected. Based on the PSA values (ng/mL) measured after 4‐to‐8 weeks of RARP, patients were divided into two groups as pPSA group (Group1)(n = 97) with PSA values ≥0.1 ng/mL and undetectable PSA group (Group2)(n = 778) with PSA values <0.1 ng/mL. Later on, Group1 was further divided into Group1a (PSA:0.1‐0.2 ng/mL) and Group 1b (PSA≥0.2 ng/mL) to evaluate biochemical recurrence(BCR). Results: Multivariate logistic regression analyses of the collected data revealed that preoperative PSA≥20 ng/mL, operation time, a postoperative international society of urological pathology (ISUP) grade of ≥4, pT 3‐4 and pN were independently associated with pPSA. Based on these results, a risk grouping algorithm predicting pPSA was developed. By looking at the risk grouping algorithm pPSA was found in 98.9% of the cases with a preoperative PSA value of ≥20 ng/mL, an operation time of 150 min, a postoperative ISUP grade of 4‐5, a positive lymphovascular invasion (LVI) status, pT3‐T4, and pN+; while pPSA was found in 25.5% of the cases with a preoperative PSA value of <20 ng/mL, an operation time of 100 min, a postoperative ISUP grade of <4‐5, a negative LVI status, pT<3‐4 and pN‐. The estimated BCR‐free survival time was 16.3 months in Group 1a and 57.0 months in Group2 ( P < .001). Adjuvant treatment ratio was 64.9% in Group1 and 7.1% in Group2 ( P < .001). Conclusion: For the patients who underwent RARP, factors associated with aggressive disease can predict the PSA persistence. To plan our treatment modalities accurately, an applicable risk grouping algorithm in daily practice would be useful.