Evidence map›Paper›PMID 40104315›Full record

ArticleTurkish journal of medical sciences2025

Predictors of Gleason score upgrading in patients with a biopsy diagnosis of grade group 1 prostate cancer.

Barış Esen, Bengi Gürses, Arif Özkan, Mert Kiliç, Yakup Kordan, Tarık Esen, Dilek Ertoy Baydar

Abstract read
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Article in Turkish journal of medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Barış EsenDepartment of Urology, Faculty of Medicine, Koç University, İstanbul, Turkiye.ORCID https://orcid.org/0000-0002-3117-4607
Bengi GürsesDepartment of Radiology, Faculty of Medicine, Koç University, İstanbul, Turkiye.ORCID https://orcid.org/0000-0002-2482-3445
Arif ÖzkanDepartment of Urology, Faculty of Medicine, Koç University, İstanbul, Turkiye.ORCID https://orcid.org/0000-0001-6534-5403
Mert KiliçDepartment of Urology, VKF AmericanHospital, İstanbul, Turkiye.ORCID https://orcid.org/0000-0003-1707-3890
Yakup KordanDepartment of Urology, Faculty of Medicine, Koç University, İstanbul, Turkiye.ORCID https://orcid.org/0000-0002-9947-848X
Tarık EsenDepartment of Urology, Faculty of Medicine, Koç University, İstanbul, Turkiye.ORCID https://orcid.org/0000-0002-0961-9374
Dilek Ertoy BaydarDepartment of Pathology, Faculty of Medicine, Koç University, İstanbul, Turkiye.ORCID https://orcid.org/0000-0003-0784-8605

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/aim: Transrectal ultrasound-guided biopsy is the most commonly used method in the diagnostic pathway of prostatic adenocarcinoma. The Gleason score of the tumor is the critical tissue-based determinant of patient management after diagnosis, and the main approach for low risk patients with grade group (GG) 1 disease is active surveillance rather than definitive interventions. However, a fair proportion of these cases are upgraded following radical prostatectomy (RP), if performed. We aimed to investigate the significance of clinicopathological parameters including phosphatase and tensin homolog (PTEN) protein in the prediction of higher final grade at RP in patients with a biopsy diagnosis of GG1 prostatic carcinoma. Materials and methods: Thirty-three patients who underwent robotic-assisted RP for grade GG1 disease at prostate biopsy were evaluated retrospectively. Their clinical, radiological, and pathological features were explored in addition to the final histological grade in RP. Upgrade was defined as any increase in Gleason score from the initial needle biopsy to pathological analysis of the entire surgical specimen. Expression of PTEN in prostate biopsy cores was evaluated through immunohistochemistry. Multivariate logistic regression was performed to detect independent predictors of tumor upgrading from biopsy to RP. Results: The final RP pathology revealed upgrading in 16 patients (48.5%) to GG2 disease. The statistics showed that Prostate Imaging Reporting and Data System score (≤3 vs. 4-5) of the index lesion and the number of involved cores in systematic biopsies (≤2 vs. >2) were the only independent predictors of the presence of a higher grade at RP (p < 0.05). The rate of PTEN loss for upgrading and nonupgrading patients was 25% and 5.9%, respectively, without statistical significance (p = 0.175). Conclusion: Multiparametric magnetic resonance imaging findings and number of tumor positive needle cores are useful parameters to apply for predicting higher grade disease in the RPs of patients with a GG1 tumor diagnosis after a prostate biopsy. Immunohistochemical PTEN analysis, on the other hand, does not provide significant information in this respect.

Indexed as

Prostatic NeoplasmsAgedHumansImage-Guided BiopsyMaleMiddle AgedNeoplasm GradingProstateProstatectomyPTEN PhosphohydrolaseRetrospective StudiesPTEN PhosphohydrolasePTEN protein, humanGleason scoregrade group 1immunohistochemistrymultiparametric magnetic resonance imagingphosphatase and tensin homologProstate cancerupgrade

Identifiers

PMID40104315
PMCPMC11913505

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.