Baco Eduard, Gelet Albert, Crouzet Sébastien, Rud Erik, Rouvière Olivier, Tonoli-Catez Hélène, Berge Viktor, Chapelon Jean-Yves, Eggesbø Heidi B
Division of Surgery and Cancer Medicine, Department of Urology Oslo University Hospital, Aker, Norway.
BJU Int. 2014 Oct;114(4):532-40. doi: 10.1111/bju.12545. Epub 2014 Apr 16.
To report the oncological and functional outcomes of hemi salvage high-intensity focused ultrasound (HSH) in patients with unilateral radiorecurrent prostate cancer.
Between 2009 and 2012, 48 patients were prospectively enrolled in two European centres. Inclusion criteria were biochemical recurrence (BCR) after primary radiotherapy (RT), positive magnetic resonance imaging and ≥1 positive biopsy in only one lobe. BCR was defined using Phoenix criteria (a rise by ≥2 ng/mL above the nadir prostate specific antigen [PSA] level). The following schemes and criteria for functional outcomes were used: Ingelman-Sundberg score using International Continence Society (ICS) questionnaire (A and B), International prostate symptom score (IPSS), International Index of Erectile Function-5 (IIEF-5) points, the European Organisation for the Research and Treatment of Cancer (EORTC) quality of life questionnaires (QLQ C-30). HSH was performed under spinal or general anaesthesia using the Ablatherm® Integrated Imaging device. Patients with obstructive voiding symptoms at the time of treatment underwent an endoscopic bladder neck resection or incision during the same anaesthesia to prevent the risk of postoperative obstruction.
After HSH the mean (sd) PSA nadir was 0.69 (0.83) ng/mL at a median (interquartile range) follow-up of 16.3 (10.5-24.5) months. Disease progression occurred in 16/48 (33%). Of these, four had local recurrence in the untreated lobe and four bilaterally, six developed metastases, and two had rising PSA levels without local recurrence or radiological confirmed metastasis. Progression-free survival rates at 12, 18, and 24 months were 83%, 64%, and 52%. Severe incontinence occurred in four of the 48 patients (8%), eight (17%) required one pad a day, and 36/48 (75%) were pad-free. The ICS questionnaire showed a mean (sd) deterioration from 0.7 (2.0) to 2.3 (4.5) for scores A and 0.6 (1.4) to 1.6 (3.0) for B. The mean (sd) IPSS and erectile function (IIEF-5) scores decreased from a mean (sd) of 7.01 (5.6) to 8.6 (5.1) and from 11.2 (8.6) to 7.0 (5.8), respectively. The mean (sd) EORTC QLC-30 scores before and after HSH were 35.7 (8.6) vs 36.8 (8.6).
HSH is a feasible therapeutic option in patients with unilateral radiorecurrent prostate cancer, which offers limited urinary and rectal morbidity, and preserves health-related quality of life.
报告半挽救性高强度聚焦超声(HSH)治疗单侧放射性复发前列腺癌患者的肿瘤学和功能结局。
2009年至2012年间,48例患者前瞻性纳入两个欧洲中心。纳入标准为初次放疗(RT)后生化复发(BCR)、磁共振成像阳性且仅一个叶有≥1次阳性活检。BCR采用Phoenix标准定义(前列腺特异性抗原[PSA]水平较最低点升高≥2 ng/mL)。使用以下方案和功能结局标准:采用国际尿控协会(ICS)问卷的英格曼-桑德伯格评分(A和B)、国际前列腺症状评分(IPSS)、国际勃起功能指数-5(IIEF-5)评分、欧洲癌症研究与治疗组织(EORTC)生活质量问卷(QLQ C-30)。使用Ablatherm®集成成像设备在脊髓麻醉或全身麻醉下进行HSH。治疗时出现梗阻性排尿症状的患者在同一次麻醉期间接受内镜膀胱颈切除术或切开术,以预防术后梗阻风险。
HSH治疗后,在中位(四分位间距)随访16.3(10.5 - 24.5)个月时,PSA最低点的均值(标准差)为0.69(0.83)ng/mL。48例患者中有16例(33%)疾病进展。其中,4例在未治疗的叶出现局部复发,4例双侧复发,6例发生转移,2例PSA水平升高但无局部复发或影像学证实的转移。12、18和24个月时的无进展生存率分别为83%、64%和52%。48例患者中有4例(8%)出现严重尿失禁,8例(17%)每天需要一片尿垫,36/48例(75%)无需使用尿垫。ICS问卷显示,A评分的均值(标准差)从0.7(2.0)降至2.3(4.5),B评分从0.6(1.4)降至1.6(3.0)。IPSS和勃起功能(IIEF-5)评分的均值(标准差)分别从7.01(5.6)降至8.6(5.1),从11.2(8.6)降至7.0(5.8)。HSH前后EORTC QLC-30评分的均值(标准差)分别为35.7(8.6)和36.8(8.6)。
HSH是单侧放射性复发前列腺癌患者的一种可行治疗选择,其泌尿和直肠发病率有限,并能保留与健康相关的生活质量。