首页> 外文会议>International Symposium on Therapeutic Ultrasound (2002- ) >Ten-year Biochemical Disease-free Survival After High-intensity Focused Ultrasound (HIFU) for Localized Prostate Cancer: Comparison with Four Different Generation Devices
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Ten-year Biochemical Disease-free Survival After High-intensity Focused Ultrasound (HIFU) for Localized Prostate Cancer: Comparison with Four Different Generation Devices

机译:高强度聚焦超声(HIFU)局部前列腺癌的10年生化无病生存:与四种不同一代装置的比较

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HIFU has been recognized as a minimally invasive treatment option for localized prostate cancer. The purpose of the study was to assess with a long-term outcome of HIFU for prostate cancer. From January 1999, a total of 657 patients who had HIFU with at least 2 year follow-up were treated with four different types of Sonablate~R (Focus Surgery, Indianapolis, USA) devices. Thirty-three patients were treated with Sonablate~R 200 (S200) from 1999 to 2001, 406 patients with Sonablate~R 500 (S500) from 2001 to 2005, 200 patients with Sonablate~R 500 version 4 (V4) from 2005-2008 and 19 patients with Sonablate~R 500 TCM (TCM) from 2007. Biochemical disease-free survival rate (bDFS) in all patients was 59% in 8 years. bDFS in 8 years in patients with S200 and S500 groups were 55% and 56%, and bDFS in 4 and 2 years in patients with V4 and TCM group were 72% and 84 %, respectively. bDFS in low, intermediate, and high risk groups were 75%, 54%, and 43% in S200/S500 and 93%, 72%, and 58% in V4/TCM group. Negative prostate biopsy rate after HIFU was 97% in S200, 79% in S500, 94% in V4 and 100% in TCM group. HIFU as primary therapy for prostate cancer is indicated in patients with low- and intermediate-risk (T1-T2b N0M0 disease, a Gleason score of <=7, a PSA level of <20 ng/mL) and a prostate volume of less than 40 mL. The rate of clinical outcome has significantly improved over the years due to technical improvements in the device.
机译:HIFU已被认为是局部前列腺癌的微创治疗选择。该研究的目的是评估HIFU的长期结果用于前列腺癌。从1999年1月起,共有657名患者患有至少2年后的HIFU的患者进行了四种不同类型的超声〜R(专注手术,印第安纳波利斯,USA)设备。从1999年到2001年的Sonablate〜R 200(S200)处理了三十三名患者,从2001年到2005年的Sonableate〜R 500(S500)的406名患者,2005年从2005-2008左右患有Sonableate〜R 500版(V4)的200名患者和19例Sonablate〜R 500 TCM(TCM)的患者从2007年患者。所有患者的生物化学疾病存活率(BDFS)在8年内为59%。 S200和S500群患者8年内的BDF为55%和56%,V4和TCM组患者4和2年的BDF分别为72%和84%。低,中间体和高风险群体的BDF为75%,54%和43%,在V4 / TCM组中为93%,72%和58%。 HIFU后的负前列腺活组织检查率在S200中为97%,在S500中的79%,v4和100%在TCM组中为94%。患有低于和中期风险(T1-T2B N0M0疾病的患者的前列腺癌的主要疗法(T1-T2B N0M0疾病,<= 7的Gleason评分,PSA水平<20ng / ml)和前列腺体积小于40毫升。由于设备技术改进,多年来临床结果的速率显着提高。

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