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Focal therapy for localized unifocal and multifocal prostate cancer: a prospective development study using real time MR guided Focused Ultrasound

机译:局灶性疗法局部大焦和多焦点前列腺癌:使用实时的前瞻性发展研究MR引导焦点超声

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To assess safety and feasibility of non-invasive high intensity 3T MR guided focused ultrasound (MRgFUS) treatment of localized prostate cancer in an exploratory designed study. Men aged 45-80 years were eligible for this prospective study if they had low-risk localized prostate cancer (prostate specific antigen [PSA] ≤10 ng/mL, Gleason score ≤ 3 + 3), with no previous androgen deprivation or treatment for prostate cancer, and who could safely undergo multiparametric MRI (Discovery 750, GE; Gd-Bopta, Bracco) and have a spinal anesthetic. Patients underwent focal therapy using real time MR guided high intensity focused ultrasound (MRgFUS), delivered to all known cancer lesions, with a margin of normal tissue. Primary endpoints were adverse events (serious and otherwise) and urinary symptoms and erectile function assessed using patient questionnaires. 8 men were recruited between June 2011 and June 2012. After treatment, one man was admitted to hospital for acute urinary retention. Another patient had self-resolving, mild, intermittent dysuria (median duration 5.0 days). Urinary tract infection was not reported. Urinary debris occurred in 6 men (75%), with a median duration of 12 days. Median overall International Index of Erectile Function-15 (IIEF-15) scores were similar at baseline and at 6 to 12 months (p=0.060), as were median IIEF-15 scores for intercourse satisfaction (p=0.433), sexual desire (p=0.622), and overall satisfaction (p=0.256). There was an improvement in lower urinary tract symptoms, assessed by International Prostate Symptom Score (IPSS), between baseline and 6 to 12 months (p=0.026). All 8 men with no baseline urinary incontinence were leak-free and pad-free by 9 months. No histological evidence of cancer was identified in 7 of 8 men biopsied at 6 months (87,5%); overall, the entire population (8 patients) was free of clinically significant cancer and had no evidence of disease on multi-parametric MRI at 6 to 12 months. MR guided Focused Ultrasound focal therapy of individual prostate cancer lesions, whether multifocal or unifocal, leads to a low rate of genitourinary side-effects and an encouraging rate of early absence of clinically significant prostate cancer.
机译:评估安全性和非侵入性的高强度3T MR引导聚焦超声(MRgFUS)治疗局限性前列腺癌中的可行性在一项探索性研究设计。男性年龄45-80年有资格获得这项前瞻性研究,如果他们有低风险局限性前列腺癌(前列腺特异性抗原[PSA]≤10毫微克/毫升,Gleason评分≤3 + 3),没有以前的雄激素剥夺或治疗前列腺癌,以及谁可以安全地进行多参数MRI(发现750,GE;钆BOPTA,布拉科),并有脊椎麻醉剂。患者接受使用实时MR引导的高强度聚焦超声(MRgFUS)聚焦治疗,传递到所有已知的癌病灶,与正常组织边缘。主要终点是不良事件(严重和其他)和泌尿系统症状,并使用患者问卷勃起功能评估。 8名男子进行了2011年6月和2012年6月之间招募的治疗后,一人被送往医院接受急性尿潴留。另一名患者有自我解决,轻度,间歇性排尿困难(中位持续时间5.0天)。没有报道尿路感染。尿碎屑发生在男性6(75%),以12天的中位数持续时间。勃起的中位总国际指数函数-15(IIEF-15)的分数在基线相似,在6至12个月(p值= 0.060),因为是为性交满意度(p值= 0.433),性欲平均IIEF-15得分( p值= 0.622),和整体满意度(p值= 0.256)。有在下尿路症状的改善,由国际前列腺症状评分(IPSS)评估,基线和6至12个月(p值= 0.026)之间。所有8名男子没有基线尿失禁是无泄漏和9个月的免费垫。癌症的无组织学证据在8人在6个月(87.5%)活检7鉴定;总体而言,整个人口(8例)是免费的临床显著癌,不得不在6〜12个月没有在多参数MRI疾病的证据。 MR引导聚焦超声个体前列腺癌病变,多灶性是否或单焦,导致的泌尿生殖副作用的低速率和早期临床缺席显著前列腺癌的鼓励率聚焦治疗。

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