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高强度聚焦超声治疗放射性复发性前列腺癌:一项北美临床试验。

High Intensity Focused Ultrasound for Radiorecurrent Prostate Cancer: A North American Clinical Trial.

作者信息

Jones Tonye A, Chin Joseph, Mcleod David, Barkin Jack, Pantuck Allan, Marks Leonard S

机构信息

Department of Urology, David Geffen School of Medicine at University of California-Los Angeles, Los Angeles, California.

Division of Urology, London Health Sciences Center, Toronto, Ontario, Canada.

出版信息

J Urol. 2018 Jan;199(1):133-139. doi: 10.1016/j.juro.2017.06.078. Epub 2017 Jun 23.

Abstract

PURPOSE

We determined the safety and efficacy of whole gland high intensity focused ultrasound in men with radiorecurrent prostate cancer.

MATERIALS AND METHODS

A total of 100 men with clinically localized recurrent prostate cancer at least 2 years after external beam radiation therapy underwent whole gland high intensity focused ultrasound in an open label trial from 2009 to 2012. Treatments were performed at 16 sites, including 14 in the United States and 2 in Canada. The primary end point was the combination of a prostate specific antigen nadir of 0.5 ng/ml or less and negative biopsy at 12 months. Validated questionnaires were administered to monitor changes in urinary and sexual function.

RESULTS

Of the 100 treated men, in whom mean age was 70 years (range 53 to 83), 78 completed the 12-month biopsy, which was negative in 63 (81%). Mean prostate specific antigen was 4.9 ng/ml (range 0.4 to 14) and the median Gleason score was 7. The 1-year end point of a prostate specific antigen nadir of 0.5 ng/ml or less plus negative biopsy was achieved in 50 men. During post-trial followup mean prostate specific antigen at 2 years was 1.1 ng/ml (range 0.1 to 17) in 33 patients. Adverse events developed in 91 men through 12 months, which were CTCAE grade 1 in 67, grade 2 in 80 and grade 3 in 20. Treatment related grade 3 adverse events included rectal fistulas in 5 men, which required surgery in 3, osteitis pubis in 3 and hematuria requiring intervention in 3. Treatment related grade 3 adverse events developed early in the trial and appeared related to operator experience. There were no life threatening adverse events or treatment related deaths.

CONCLUSIONS

Whole gland high intensity focused ultrasound appears reasonably safe and effective to treat radiorecurrent prostate cancer. The rate of complications, which are potentially severe, was acceptable, especially considering the advanced, refractory nature of the disease and the limited treatment options.

摘要

目的

我们确定了全腺体高强度聚焦超声治疗放射性复发性前列腺癌男性患者的安全性和有效性。

材料与方法

2009年至2012年,共有100名在体外放疗后至少2年出现临床局限性复发性前列腺癌的男性患者,在一项开放标签试验中接受了全腺体高强度聚焦超声治疗。治疗在16个地点进行,包括美国的14个地点和加拿大的2个地点。主要终点是前列腺特异性抗原最低点为0.5 ng/ml或更低且12个月时活检阴性。使用经过验证的问卷来监测泌尿和性功能的变化。

结果

在100名接受治疗的男性患者中,平均年龄为70岁(范围53至83岁),78人完成了12个月的活检,其中63人(81%)活检结果为阴性。平均前列腺特异性抗原为4.9 ng/ml(范围0.4至14),Gleason评分中位数为7。50名男性患者达到了前列腺特异性抗原最低点为0.5 ng/ml或更低且活检阴性的1年终点。在试验后的随访中,33例患者在2年时的平均前列腺特异性抗原为1.1 ng/ml(范围0.1至17)。91名男性患者在12个月内出现了不良事件,其中67例为CTCAE 1级,80例为2级,20例为3级。与治疗相关的3级不良事件包括5名男性出现直肠瘘,其中3人需要手术治疗,3人出现耻骨炎,3人出现需要干预的血尿。与治疗相关的3级不良事件在试验早期出现,似乎与操作者经验有关。没有危及生命的不良事件或与治疗相关的死亡。

结论

全腺体高强度聚焦超声治疗放射性复发性前列腺癌似乎相当安全有效。并发症发生率虽可能较严重,但可以接受,尤其是考虑到该疾病的晚期、难治性本质以及有限的治疗选择。

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