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局部低危或中危前列腺癌消融的焦点与扩展不可逆电穿孔治疗的早期肿瘤控制效果:一项随机临床试验。

Effect of Focal vs Extended Irreversible Electroporation for the Ablation of Localized Low- or Intermediate-Risk Prostate Cancer on Early Oncological Control: A Randomized Clinical Trial.

机构信息

Department of Urology, Beijing United Family Hospital and Clinics, Beijing, China.

S.H. Ho Urology Centre, Department of Surgery, Chinese University of Hong Kong, Hong Kong, China.

出版信息

JAMA Surg. 2023 Apr 1;158(4):343-349. doi: 10.1001/jamasurg.2022.7516.

Abstract

IMPORTANCE

Focal ablative irreversible electroporation (IRE) is a therapy that treats only the area of the tumor with the aim of achieving oncological control while reducing treatment-related functional detriment.

OBJECTIVE

To evaluate the effect of focal vs extended IRE on early oncological control for patients with localized low- and intermediate-risk prostate cancer.

DESIGN, SETTING, AND PARTICIPANTS: In this randomized clinical trial conducted at 5 centers in Europe, men with localized low- to intermediate-risk prostate cancer were randomized to receive either focal or extended IRE ablation. Data were collected at baseline and at regular intervals after the procedure from June 2015 to January 2020, and data were analyzed from September 2021 to July 2022.

MAIN OUTCOMES AND MEASURES

Oncological outcome as indicated by presence of clinically significant prostate cancer (International Society of Urological Pathology grade ≥2) on transperineal template-mapping prostate biopsy at 6 months after IRE. Descriptive measures of results from that biopsy included the number and location of positive cores.

RESULTS

A total of 51 and 55 patients underwent focal and extended IRE, respectively. Median (IQR) age was 64 years (58-67) in the focal ablation group and 64 years (57-68) in the extended ablation group. Median (IQR) follow-up time was 30 months (24-48). Clinically significant prostate cancer was detected in 9 patients (18.8%) in the focal ablation group and 7 patients (13.2%) in the extended ablation group. There was no significant difference in presence of clinically significant prostate cancer between the 2 groups. In the focal ablation group, 17 patients (35.4%) had positive cores outside of the treated area, 3 patients (6.3%) had positive cores in the treated area, and 5 patients (10.4%) had positive cores both in and outside of the treated area. In the extended group, 10 patients (18.9%) had positive cores outside of the treated area, 9 patients (17.0%) had positive cores in the treated area, and 2 patients (3.8%) had positive cores both in and outside of the treated area. Clinically significant cancer was found in the treated area in 5 of 48 patients (10.4%) in the focal ablation group and 5 of 53 patients (9.4%) in the extended ablation group.

CONCLUSIONS AND RELEVANCE

This study found that focal and extended IRE ablation achieved similar oncological outcomes in men with localized low- or intermediate-risk prostate cancer. Because some patients with intermediate-risk prostate cancer are still candidates for active surveillance, focal therapy may be a promising option for those patients with a high risk of cancer progression.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT01835977.

摘要

重要性

局灶性消融不可逆电穿孔(IRE)是一种仅治疗肿瘤区域的治疗方法,旨在实现肿瘤控制,同时减少治疗相关的功能损害。

目的

评估局灶性与扩展性 IRE 对局部低危和中危前列腺癌患者早期肿瘤控制的影响。

设计、地点和参与者:这项在欧洲 5 个中心进行的随机临床试验中,将局部低危至中危前列腺癌患者随机分配接受局灶性或扩展性 IRE 消融治疗。数据于 2015 年 6 月至 2020 年 1 月期间在基线和手术后定期收集,数据分析于 2021 年 9 月至 2022 年 7 月进行。

主要结果和测量指标

IRE 后 6 个月经会阴模板映射前列腺活检证实存在临床显著前列腺癌(国际泌尿病理学会分级≥2 级)的肿瘤学结果。活检结果的描述性指标包括阳性核心的数量和位置。

结果

共有 51 名和 55 名患者分别接受了局灶性和扩展性 IRE 治疗。局灶性消融组中位(IQR)年龄为 64 岁(58-67),扩展性消融组为 64 岁(57-68)。中位(IQR)随访时间为 30 个月(24-48)。局灶性消融组有 9 名(18.8%)患者和扩展性消融组有 7 名(13.2%)患者检测到临床显著前列腺癌。两组间存在临床显著前列腺癌的比例无显著差异。在局灶性消融组,17 名(35.4%)患者在治疗区域外有阳性核心,3 名(6.3%)患者在治疗区域内有阳性核心,5 名(10.4%)患者在治疗区域内外均有阳性核心。在扩展组中,10 名(18.9%)患者在治疗区域外有阳性核心,9 名(17.0%)患者在治疗区域内有阳性核心,2 名(3.8%)患者在治疗区域内外均有阳性核心。局灶性消融组有 5 名(10.4%)患者在治疗区域内发现有临床显著的癌症,扩展性消融组有 5 名(9.4%)患者在治疗区域内发现有临床显著的癌症。

结论和相关性

这项研究发现,局灶性和扩展性 IRE 消融在局部低危或中危前列腺癌患者中获得了相似的肿瘤学结果。由于一些中危前列腺癌患者仍适合主动监测,因此对于那些癌症进展风险较高的患者,局灶性治疗可能是一种很有前途的选择。

试验注册

ClinicalTrials.gov 标识符:NCT01835977。

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