Department of Urology and Pediatric Urology, University Medical Center, Mainz, Germany;Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA;Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Department of Urology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Diagn Interv Radiol. 2021 May;27(3):394-400. doi: 10.5152/dir.2021.20095.
We aimed to assess post-interventional and 36-month follow-up results of a single-center, single-arm, in-bore phase I trial of focal laser ablation (FLA) guided by multiparametric magnetic resonance imaging (mpMRI).
FLA procedures were done in-bore MRI using a transperineal approach. Primary endpoints were feasibility and safety expressed as lack of grade 3 complications. Secondary endpoints were changes in international prostate symptom score (IPSS), sexual health inventory for men (SHIM), quality of life (QoL) scores, and serum prostate specific antigen (PSA) levels. Treatment outcomes were assessed by combined mpMRI-ultrasound fusion-guided and extended sextant systematic biopsy after 12, 24, and optionally after 36 months.
Fifteen participants were included. Seven patients (46.67%) had Gleason 3+3 and 8 patients (53.33%) had Gleason 3+4 cancer. All patients tolerated the procedure well, and no grade 3/4 complications occurred. All grade 1 and 2 complications were transient and resolved completely. There was no significant change in mean IPSS from baseline (-1, p = 0.460) and QoL (0, p = 0.441) scores following FLA but there was a significant drop in mean SHIM scores (-2, p = 0.010) compared to pretreatment baselines. Mean PSA significantly decreased after FLA (-2.5, p < 0.001). Seven out of 15 patients (46.67%) had residual cancer in, adjacent, or in close proximity to the treatment area (1 × 4+3=7, 1 × 3+4=7, and 5 × 3+3=6). Four out of 15 patients (26.67%) underwent salvage therapy (2 repeat FLA, 2 radical prostatectomy).
After 3 years of follow-up we conclude focal laser ablation is safe and feasible without significant complications.
我们旨在评估单中心、单臂、腔内一期试验中多参数磁共振成像(mpMRI)引导下的局灶性激光消融(FLA)的介入后和 36 个月随访结果。
FLA 手术在腔内 MRI 下经会阴入路进行。主要终点为缺乏 3 级并发症的可行性和安全性。次要终点为国际前列腺症状评分(IPSS)、男性性功能健康问卷(SHIM)、生活质量(QoL)评分和血清前列腺特异性抗原(PSA)水平的变化。治疗结果通过 12、24 个月后和选择性 36 个月后联合 mpMRI-超声融合引导和扩展六分系统活检进行评估。
共纳入 15 名参与者。7 名患者(46.67%)患有 Gleason 3+3 癌,8 名患者(53.33%)患有 Gleason 3+4 癌。所有患者均能很好地耐受该手术,且无 3/4 级并发症发生。所有 1/2 级并发症均为一过性,完全缓解。与 FLA 前相比,平均 IPSS(-1,p=0.460)和 QoL(0,p=0.441)评分无显著变化,但平均 SHIM 评分显著下降(-2,p=0.010)。与 FLA 前相比,平均 PSA 显著下降(-2.5,p<0.001)。15 名患者中有 7 名(46.67%)在治疗区域内、相邻区域或附近有残留癌症(1×4+3=7,1×3+4=7,5×3+3=6)。15 名患者中有 4 名(26.67%)接受了挽救性治疗(2 次重复 FLA,2 次根治性前列腺切除术)。
随访 3 年后,我们得出结论,局灶性激光消融是安全可行的,无明显并发症。