Wimper Yvonne, Te Molder Lauren P W, Sedelaar J P Michiel, Bomers Joyce G R, Overduin Christiaan G, Fütterer Jurgen J
Department of Medical Imaging, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Department of Medical Imaging, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
J Vasc Interv Radiol. 2025 May;36(5):795-804. doi: 10.1016/j.jvir.2025.01.043. Epub 2025 Jan 28.
To investigate the feasibility and safety of magnetic resonance (MR) imaging-guided focal laser ablation (FLA) in localized, International Society of Urological Pathology (ISUP) Grade 1-3, prostate cancer (PCa) using an integrated system.
Ten consecutive males (mean age, 66 years [SD ± 7]) with low-to-intermediate-risk PCa were prospectively included (April 2022-May 2023) and treated with MR imaging-guided FLA using an integrated system for laser energy control and MR thermometry monitoring. Primary end points were technical success, procedure-related adverse events (AEs) following Society of Interventional Radiology (SIR) classification, and 12-month local tumor progression-free survival, defined as no evident residual/recurrent disease on follow-up imaging or histopathology at the treatment site. Secondary end points included MR imaging-derived volumetric tumor coverage percentage, prostate-specific antigen (PSA) levels, and sexual and urinary function response measured by the Sexual Health Inventory for Men (SHIM) and International Prostate Symptom Score (IPSS) index questionnaires, respectively.
Technical success was achieved in all 10 (100%) patients (ISUP Grade 1, n = 1; Grade 2, n = 8; and Grade 3, n = 1). Three AEs were observed: urinary tract infection (n = 2; SIR Grade 2) and acute urinary retention (n = 1; SIR Grade 3). Cumulative 12-month local tumor progression-free survival was 80% (8/10 patients). Median tumor coverage was 100% (IQR, 95%-100%). Compared with baseline, the mean PSA level decreased, but did not reach statistical significance (6.6 vs 4.4 ng/mL; P = .06), and mean urinary (8.6 vs 7.3; P = 0.60) and sexual function (11.3 vs 10.5; P = 1.00) scores were nonsignificantly altered at 12-month follow-up.
MR imaging-guided FLA in patients with low-to-intermediate-risk PCa using an integrated system was feasible and safe and resulted in promising short-term oncologic and functional outcomes.
使用集成系统研究磁共振(MR)成像引导下聚焦激光消融(FLA)治疗局限性国际泌尿病理学会(ISUP)1 - 3级前列腺癌(PCa)的可行性和安全性。
前瞻性纳入10例连续的低至中危PCa男性患者(平均年龄66岁[标准差±7])(2022年4月至2023年5月),使用集成系统进行激光能量控制和MR温度监测,接受MR成像引导下的FLA治疗。主要终点为技术成功、按照介入放射学会(SIR)分类的与手术相关的不良事件(AE)以及12个月局部肿瘤无进展生存率,定义为随访成像或治疗部位组织病理学检查未发现明显残留/复发病变。次要终点包括MR成像得出的肿瘤体积覆盖百分比、前列腺特异性抗原(PSA)水平,以及分别通过男性性健康量表(SHIM)和国际前列腺症状评分(IPSS)指数问卷测量的性功能和排尿功能反应。
所有10例(100%)患者均取得技术成功(ISUP 1级,n = 1;2级,n = 8;3级,n = 1)。观察到3例AE:尿路感染(n = 2;SIR 2级)和急性尿潴留(n = 1;SIR 3级)。12个月累积局部肿瘤无进展生存率为80%(8/10例患者)。肿瘤覆盖中位数为100%(四分位间距,95% - 100%)。与基线相比,平均PSA水平下降,但未达到统计学意义(6.6 vs 4.4 ng/mL;P = 0.06),12个月随访时平均排尿功能评分(8.6 vs 7.3;P = 0.60)和性功能评分(11.3 vs 10.5;P = 1.00)无显著变化。
使用集成系统对低至中危PCa患者进行MR成像引导下的FLA是可行且安全的,并产生了有前景的短期肿瘤学和功能学结果。