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Risk‐Stratified Gleason Upgrading in ISUP Grade Group 1 Prostate Cancer: Combined Analysis of TMPRSS2 ‐ ERG , PTEN , Ki‐67, and MRI ‐Derived Apparent Diffusion Coefficient Values

医学 前列腺 泌尿科 有效扩散系数 扩散 核医学 群(周期表) 前列腺癌 显著性差异 统计分析 前列腺疾病 变异系数
作者
Nursinem Alkan Vurğun,Nilay Şen Türk,Sercan Vurğun,Ahmet Baki Yağcı,Sinan ÇELEN,Mesut Berkan Duran
出处
期刊:International Journal of Urology [Wiley]
卷期号:33 (1): e70346-e70346
标识
DOI:10.1111/iju.70346
摘要

ABSTRACT Objective To evaluate molecular, immunohistochemical, and radiological parameters associated with pathological upgrading in patients with ISUP Grade Group 1 (GG1) prostate cancer who underwent radical prostatectomy (RP). Methods A total of 106 patients diagnosed with ISUP GG1 prostate adenocarcinoma via needle biopsy and treated with RP between 2012 and 2022 were retrospectively analyzed. Based on final pathology, patients were categorized into No Upgrade, Low‐risk Upgrade, and High‐risk Upgrade groups. Biopsy specimens were evaluated for PTEN, ERG, and Ki‐67 expression and TMPRSS2‐ERG gene fusion status, while radiological parameters, including PI‐RADS v2.1 scores and ADC values (ADC tumor and ADC ratio ), were assessed based on preoperative multiparametric MRI. Results TMPRSS2‐ERG fusion positivity and elevated ERG expression were significantly more common in the High‐risk Upgrade group ( p < 0.01 and p = 0.04, respectively). PI‐RADS scores showed a stepwise increase, and ADC tumor values decreased across risk groups ( p = 0.01 and p = 0.03). No significant differences were observed for PTEN loss, Ki‐67 index, or ADC ratio . Conclusion Certain immunohistochemical, radiological, and molecular parameters may be predictive of pathological upgrading in GG1 prostate cancer. Incorporation of these biomarkers into diagnostic evaluation and treatment planning may aid in refining risk stratification and avoiding overtreatment in clinically indolent cases. Although ADC tumor values were significantly associated with upgrading, their correlation with molecular markers such as PTEN, ERG, Ki‐67, and TMPRSS2‐ERG fusion were not statistically significant. Trial Registration Project No: 2023TIPF001
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