Masatomo Kaneko, Lorenzo Storino Ramacciotti, Yuta Inoue, Samuel Peretsman, Jessica Cummins, Jie Cai, Pierre Halteh, Suzanne Palmer, Manju Aron, Osamu Ukimura, Inderbir S. Gill, Andre Luis Abreu
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The primary endpoint was treatment failure (TF), defined as Grade Group (GG) ≥ 2 on follow-up PBx (FU-PBx), any whole-gland treatment, systemic therapy, metastases or PCa-specific mortality. Kaplan–Meier and Cox regression analyses were performed. Statistically significant if p < 0.05.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>A total of 156 patients met the inclusion criteria being 96 (62%) high-visibility and 59 (38%) low-visibility groups on baseline MRI. The baseline characteristics were as follows: median age 65yo, prostate-specific antigen (PSA) 6.0 ng/ml, 22% with PIRADS 1–2, 16% with PIRADS 3, 44% with PIRADS 4 and 17% with PIRADS 5. The 3-year free-survival rates for high-visible vs low-visible were: TF 57% vs 83% (p = 0.002); biochemical failure (PSA nadir + 2 ng/ml) 81% vs 72% (p = 0.5); GG ≥ 2 on FU-PBx 57% vs 85% (p < 0.001); and Radical Treatment 87% vs 85% (p = 0.9), respectively. After adjusting for confounders, the independent predictors for TF were PSA density, PSA reduction and high visibility (hazard ratio 4.83, 95% confidence interval 1.81–12.90).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>MRI visibility is an independent prognosticator for outcomes following focal therapy for prostate cancer. Patients with higher MRI visibility (PIRADS ≥4) are at an increased risk of treatment failure.</p>\n </section>\n </div>","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"6 8","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12328995/pdf/","citationCount":"0","resultStr":"{\"title\":\"Impact of magnetic resonance imaging visibility of prostate cancer on partial gland ablation\",\"authors\":\"Masatomo Kaneko, Lorenzo Storino Ramacciotti, Yuta Inoue, Samuel Peretsman, Jessica Cummins, Jie Cai, Pierre Halteh, Suzanne Palmer, Manju Aron, Osamu Ukimura, Inderbir S. Gill, Andre Luis Abreu\",\"doi\":\"10.1002/bco2.70065\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Objectives</h3>\\n \\n <p>To evaluate the outcomes of partial gland ablation (PGA) according to prostate cancer (PCa) visibility on magnetic resonance imaging (MRI).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Subjects and Methods</h3>\\n \\n <p>Consecutive patients with localized PCa diagnosed by MRI-informed prostate biopsy (PBx), who underwent hemi-gland Cryoablation (CRYO) or hemi-gland High-Intensity Focused Ultrasound (HIFU), were identified from a multicentric database. High-visibility was defined as Prostate Imaging–Reporting and Data System (PIRADS) ≥ 4. The primary endpoint was treatment failure (TF), defined as Grade Group (GG) ≥ 2 on follow-up PBx (FU-PBx), any whole-gland treatment, systemic therapy, metastases or PCa-specific mortality. Kaplan–Meier and Cox regression analyses were performed. 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引用次数: 0
摘要
目的:根据前列腺癌(PCa)在磁共振成像(MRI)上的可见性,评价部分腺体消融(PGA)的治疗效果。研究对象和方法:从一个多中心数据库中识别出连续的经mri前列腺活检(PBx)诊断为局部PCa的患者,这些患者接受了半腺体冷冻消融(CRYO)或半腺体高强度聚焦超声(HIFU)。高可见性定义为前列腺成像报告和数据系统(PIRADS)≥4。主要终点是治疗失败(TF),定义为随访PBx (FU-PBx)分级组(GG)≥2,任何全腺体治疗,全身治疗,转移或pca特异性死亡率。Kaplan-Meier和Cox回归分析。结果:156例患者符合纳入标准,其中基线MRI高能见度组96例(62%),低能见度组59例(38%)。基线特征如下:中位年龄65岁,前列腺特异性抗原(PSA) 6.0 ng/ml, PIRADS 1-2为22%,PIRADS 3为16%,PIRADS 4为44%,PIRADS 5为17%。高可见与低可见的3年自由生存率分别为:TF 57% vs 83% (p = 0.002);生化失败(PSA nadir + 2 ng/ml) 81% vs 72% (p = 0.5);结论:MRI可见性是前列腺癌局灶治疗后预后的独立预测指标。MRI可见性较高(PIRADS≥4)的患者治疗失败的风险增加。
Impact of magnetic resonance imaging visibility of prostate cancer on partial gland ablation
Objectives
To evaluate the outcomes of partial gland ablation (PGA) according to prostate cancer (PCa) visibility on magnetic resonance imaging (MRI).
Subjects and Methods
Consecutive patients with localized PCa diagnosed by MRI-informed prostate biopsy (PBx), who underwent hemi-gland Cryoablation (CRYO) or hemi-gland High-Intensity Focused Ultrasound (HIFU), were identified from a multicentric database. High-visibility was defined as Prostate Imaging–Reporting and Data System (PIRADS) ≥ 4. The primary endpoint was treatment failure (TF), defined as Grade Group (GG) ≥ 2 on follow-up PBx (FU-PBx), any whole-gland treatment, systemic therapy, metastases or PCa-specific mortality. Kaplan–Meier and Cox regression analyses were performed. Statistically significant if p < 0.05.
Results
A total of 156 patients met the inclusion criteria being 96 (62%) high-visibility and 59 (38%) low-visibility groups on baseline MRI. The baseline characteristics were as follows: median age 65yo, prostate-specific antigen (PSA) 6.0 ng/ml, 22% with PIRADS 1–2, 16% with PIRADS 3, 44% with PIRADS 4 and 17% with PIRADS 5. The 3-year free-survival rates for high-visible vs low-visible were: TF 57% vs 83% (p = 0.002); biochemical failure (PSA nadir + 2 ng/ml) 81% vs 72% (p = 0.5); GG ≥ 2 on FU-PBx 57% vs 85% (p < 0.001); and Radical Treatment 87% vs 85% (p = 0.9), respectively. After adjusting for confounders, the independent predictors for TF were PSA density, PSA reduction and high visibility (hazard ratio 4.83, 95% confidence interval 1.81–12.90).
Conclusion
MRI visibility is an independent prognosticator for outcomes following focal therapy for prostate cancer. Patients with higher MRI visibility (PIRADS ≥4) are at an increased risk of treatment failure.