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经直肠高强度聚焦超声治疗对前列腺癌的局部控制:初步结果。

Local control of prostate cancer by transrectal high intensity focused ultrasound therapy: preliminary results.

作者信息

Gelet A, Chapelon J Y, Bouvier R, Pangaud C, Lasne Y

机构信息

Urology Department, Edouard Herriot Hospital and INSERM Unité 281, Lyon, France.

出版信息

J Urol. 1999 Jan;161(1):156-62.

Abstract

PURPOSE

We conducted a phase I/II study to evaluate the efficacy of transrectal high intensity focused ultrasound in the treatment of localized prostate cancer and to assess associated complications. The efficacy of a new high intensity ultrasound device was evaluated using post-treatment prostate specific antigen (PSA) levels and histological results from prostate biopsies as end points.

MATERIALS AND METHODS

A total of 113 transrectal high intensity focused ultrasound sessions were performed in 50 patients with localized prostate cancer, who were not suitable candidates for radical prostatectomy. Of these patients 2 underwent salvage ultrasound treatment for locally recurrent cancer following definitive radiation therapy. Mean plus or minus standard deviation patient age, PSA and prostate volume were 70.7+/-4.54 years, 9.61+/-7.42 ng./ml. and 37.3+/-19.1 cc. The 2 different high intensity ultrasound prototypes were successfully used, and the latter prototype included several safety devices to reduce morbidity. Median followup was 24 months (range 3 to 46). Control parameters were changes in PSA and random control sextant biopsies at 1 to 3, 3 to 12, 12 to 24, 24 to 36 and 36 to 48 months.

RESULTS

For the evaluation of therapy patients were divided into 4 groups. Group 1 (complete response) included 28 patients (56%) with no residual cancer and PSA less than 4 ng./ml. (mean 0.93), group 2 (biochemical failure) 3 patients (6%) with no residual cancer and PSA greater than 4 ng./ml. (mean 6.22), group 3 (biochemical control) 9 patients (18%) with residual cancer (mean positive biopsy 1.1 of 6) and PSA less than 4 ng./ml. (mean 0.90), and group 4 (failures) 10 patients (20%) with residual cancer (mean positive biopsies 1.9 of 6) and PSA greater than 4 ng./ml. (mean 8.9). Of the 10 cases in group 4 hormone therapy was required in 3 and radiotherapy in 5. Complication rate with the first prototype device was 50% and it decreased to 17% with the second prototype.

CONCLUSIONS

Morbidity associated with high intensity focused ultrasound treatment is currently minimal. Local control of the localized prostate cancer was observed in groups 1, 2 and 3 (80%). Repeat sessions were deferred in groups 2 and 3 based on changes in PSA. These preliminary data suggest that high intensity focused ultrasound represents a valid alternative treatment strategy for patients with localized prostate cancer who are unsuitable for surgery.

摘要

目的

我们开展了一项I/II期研究,以评估经直肠高强度聚焦超声治疗局限性前列腺癌的疗效,并评估相关并发症。使用治疗后的前列腺特异性抗原(PSA)水平以及前列腺活检的组织学结果作为终点,评估一种新型高强度超声设备的疗效。

材料与方法

对50例局限性前列腺癌患者进行了总共113次经直肠高强度聚焦超声治疗,这些患者不适合进行根治性前列腺切除术。其中2例患者在确定性放射治疗后因局部复发性癌症接受了挽救性超声治疗。患者的平均年龄(标准差)、PSA水平和前列腺体积分别为70.7±4.54岁、9.61±7.42 ng/ml和37.3±19.1 cc。成功使用了2种不同的高强度超声原型,后一种原型包括几种安全装置以降低发病率。中位随访时间为24个月(范围3至46个月)。对照参数为1至3个月、3至12个月、12至24个月、24至36个月以及36至48个月时PSA的变化和随机对照六分区活检结果。

结果

为评估治疗效果,将患者分为4组。第1组(完全缓解)包括28例患者(56%),无残留癌症且PSA低于4 ng/ml(平均0.93);第2组(生化失败)3例患者(6%),无残留癌症但PSA高于4 ng/ml(平均6.22);第3组(生化控制)9例患者(18%),有残留癌症(平均6个活检样本中有1.1个呈阳性)且PSA低于4 ng/ml(平均0.90);第4组(失败)10例患者(20%),有残留癌症(平均6个活检样本中有1.9个呈阳性)且PSA高于4 ng/ml(平均8.9)。第4组的10例患者中,3例需要激素治疗,5例需要放射治疗。第一种原型设备的并发症发生率为50%,第二种原型设备的并发症发生率降至17%。

结论

目前,高强度聚焦超声治疗相关的发病率极低。在第1、2和3组(80%)中观察到局限性前列腺癌得到了局部控制。根据PSA的变化,第2组和第3组推迟了重复治疗。这些初步数据表明,对于不适合手术的局限性前列腺癌患者,高强度聚焦超声是一种有效的替代治疗策略。

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