Assessment of the optimal number of positive biopsy cores to discriminate between cancer-specific mortality in high-risk versus very high-risk prostate cancer patients
Language English Country United States Media print-electronic
Document type Journal Article
PubMed
34312910
DOI
10.1002/pros.24202
Knihovny.cz E-resources
- Keywords
- NCCN, biopsy cores, high risk, prostate cancer, very high risk,
- MeSH
- Adenocarcinoma mortality pathology surgery MeSH
- Biopsy, Large-Core Needle MeSH
- Risk Assessment MeSH
- Middle Aged MeSH
- Humans MeSH
- Survival Rate MeSH
- Prostatic Neoplasms mortality pathology surgery MeSH
- SEER Program MeSH
- Prostate pathology MeSH
- Prostatectomy MeSH
- Retrospective Studies MeSH
- Aged MeSH
- Neoplasm Grading MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
BACKGROUND: Number of positive prostate biopsy cores represents a key determinant between high versus very high-risk prostate cancer (PCa). We performed a critical appraisal of the association between the number of positive prostate biopsy cores and CSM in high versus very high-risk PCa. METHODS: Within Surveillance, Epidemiology, and End Results database (2010-2016), 13,836 high versus 20,359 very high-risk PCa patients were identified. Discrimination according to 11 different positive prostate biopsy core cut-offs (≥2-≥12) were tested in Kaplan-Meier, cumulative incidence, and multivariable Cox and competing risks regression models. RESULTS: Among 11 tested positive prostate biopsy core cut-offs, more than or equal to 8 (high-risk vs. very high-risk: n = 18,986 vs. n = 15,209, median prostate-specific antigen [PSA]: 10.6 vs. 16.8 ng/ml, <.001) yielded optimal discrimination and was closely followed by the established more than or equal to 5 cut-off (high-risk vs. very high-risk: n = 13,836 vs. n = 20,359, median PSA: 16.5 vs. 11.1 ng/ml, p < .001). Stratification according to more than or equal to 8 positive prostate biopsy cores resulted in CSM rates of 4.1 versus 14.2% (delta: 10.1%, multivariable hazard ratio: 2.2, p < .001) and stratification according to more than or equal to 5 positive prostate biopsy cores with CSM rates of 3.7 versus 11.9% (delta: 8.2%, multivariable hazard ratio: 2.0, p < .001) in respectively high versus very high-risk PCa. CONCLUSIONS: The more than or equal to 8 positive prostate biopsy cores cutoff yielded optimal results. It was very closely followed by more than or equal to 5 positive prostate biopsy cores. In consequence, virtually the same endorsement may be made for either cutoff. However, more than or equal to 5 positive prostate biopsy cores cutoff, based on its existing wide implementation, might represent the optimal choice.
Department of Urology 2nd Faculty of Medicine Charles University Prag Czech Republic
Department of Urology Comprehensive Cancer Center Medical University of Vienna Vienna Austria
Department of Urology Policlinico San Martino Hospital University of Genova Genova Italy
Department of Urology University Hospital Frankfurt Frankfurt am Main Germany
Department of Urology University Hospital Hamburg Eppendorf Hamburg Germany
Department of Urology University of Texas Southwestern Dallas Texas USA
Departments of Urology Weill Cornell Medical College New York New York USA
Martini Klinik Prostate Cancer Center University Hospital Hamburg Eppendorf Hamburg Germany
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Mohler JL, Antonarakis ES, Armstrong AJ, et al. Prostate cancer, version 1.2020, NCCN clinical practice guidelines in oncology. J Natl Compr Canc Netw. 2020.
Sundi D, Wang VM, Pierorazio PM, et al. Very-high-risk localized prostate cancer: definition and outcomes. Prostate Cancer Prostatic Dis. 2014;17(1):57-63.
Wang Y, Song P, Wang J, Shu M, Wang Q, Li Q. Superior survival benefits of radical prostatectomy than external beam radiotherapy in aging 75 and older men with high-risk or very high-risk prostate cancer: a population-matched study. J Cancer. 2020;11(18):5371-5378.
Sakurai T, Takamatsu S, Shibata S, et al. Toxicity and clinical outcomes of single-fraction high-dose-rate brachytherapy combined with external beam radiotherapy for high-/very high-risk prostate cancer: a dosimetric analysis of toxicity. Jpn J Radiol. 2020;38(12):1197-1208.
Kasahara T, Ishizaki F, Kazama A, et al. High-dose-rate brachytherapy and hypofractionated external beam radiotherapy combined with long-term androgen deprivation therapy for very high-risk prostate cancer. Int J Urol. 2020;27(9):800-806.
Wang S-C, Ting W-C, Chang Y-C, et al. Whole pelvic radiotherapy with stereotactic body radiotherapy boost vs. conventionally fractionated radiotherapy for patients with high or very high-risk prostate cancer. Front Oncol. 2020;10:814.
Ranasinghe W, Reichard CA, Nyame YA, et al. Downgrading from biopsy grade group 4 prostate cancer in patients undergoing radical prostatectomy for high or very high risk prostate cancer. J Urol. 2020;204(4):748-753.
Kliment J, Elias B, Baluchova K, Kliment J. The long-term outcomes of radical prostatectomy for very high-risk prostate cancer pT3b-T4 N0-1 on definitive histopathology. Cent European J Urol. 2017;70(1):13-19.
Stattin P, Sandin F, Thomsen FB, et al. Association of radical local treatment with mortality in men with very high-risk prostate cancer: a semiecologic, nationwide, population-based study. Eur Urol. 2017;72(1):125-134.
Koo KC, Jung DC, Lee SH, et al. Feasibility of robot-assisted radical prostatectomy for very-high risk prostate cancer: surgical and oncological outcomes in men aged ≥70 years. Prostate Int. 2014;2(3):127-132.
Shilkrut M, McLaughlin PW, Merrick GS, Vainshtein JM, Hamstra DA. Treatment Outcomes in Very High-risk Prostate Cancer Treated by Dose-escalated and Combined-Modality Radiation Therapy. Am J Clin Oncol. 2016;39(2):181-188.
Reichard CA, Hoffman KE, Tang C, et al. Radical prostatectomy or radiotherapy for high- and very high-risk prostate cancer: a multidisciplinary prostate cancer clinic experience of patients eligible for either treatment. BJU Int. 2019;124(5):811-819.
Pompe RS, Karakiewicz PI, Tian Z, et al. Oncologic and functional outcomes after radical prostatectomy for high or very high risk prostate cancer: European validation of the current NCCN® Guideline. J Urol. 2017;198(2):354-361.
Sundi D, Tosoian JJ, Nyame YA, et al. Outcomes of very high-risk prostate cancer after radical prostatectomy: validation study from 3 centers. Cancer. 2019;125(3):391-397.
Saad A, Goldstein J, Lawrence YR, et al. Classifying high-risk versus very high-risk prostate cancer: is it relevant to outcomes of conformal radiotherapy and androgen deprivation? Radiat Oncol. 2017;12(1):5.
About the SEER Program [Internet]. SEER. 2021. https://seer.cancer.gov/about/overview.html
Wenzel M, Würnschimmel C, Collà Ruvolo C, et al. Increasing rates of NCCN high and very high-risk prostate cancer vs. number of prostate biopsy cores. Prostate. In press.
Wenzel M, Würnschimmel C, Chierigo F, et al. Non-cancer mortality in elderly prostate cancer patients treated with combination of radical prostatectomy and external beam radiation therapy. Prostate. 2021;81:728-735. https://doi.org/10.1002/pros.24169
Knipper S, Karakiewicz PI, Heinze A, et al. Definition of high-risk prostate cancer impacts oncological outcomes after radical prostatectomy. Urol Oncol. 2020;38(4):184-190.
Tilki D, Mandel P, Karakiewicz PI, et al. The impact of very high initial PSA on oncological outcomes after radical prostatectomy for clinically localized prostate cancer. Urol Oncol. 2020;38(5):379-385.
Knipper S, Pecoraro A, Palumbo C, et al. A 25-year period analysis of other-cause mortality in localized prostate cancer. Clin Genitourin Cancer. 2019;17(5):395-401.
Bandini M, Preisser F, Nazzani S, et al. The effect of other-cause mortality adjustment on access to alternative treatment modalities for localized prostate cancer among african american patients. Eur Urol Oncol. 2018;1(3):215-222.
Bernatz S, Ackermann J, Mandel P, et al. Comparison of machine learning algorithms to predict clinically significant prostate cancer of the peripheral zone with multiparametric MRI using clinical assessment categories and radiomic features. Eur Radiol. 2020;30(12):6757-6769. https://doi.org/10.1007/s00330-020-07064-5
Preisser F, Theissen L, Wenzel M, et al. Performance of combined magnetic resonance imaging/ultrasound fusion-guided and systematic biopsy of the prostate in biopsy-naïve patients and patients with prior biopsies. Eur Urol Focus. 2021;7(1):39-46. https://doi.org/10.1016/j.euf.2019.06.015
Rührup J, Preisser F, Theißen L, et al. MRI-fusion targeted vs. systematic prostate biopsy-how does the biopsy technique affect gleason grade concordance and upgrading after radical prostatectomy? Front Surg. 2019;6:55. https://doi.org/10.3389/fsurg.2019.00055