Icon Cancer Centre, Richmond, VIC, Australia.
Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
World J Urol. 2021 Nov;39(11):4117-4125. doi: 10.1007/s00345-021-03735-0. Epub 2021 Jun 2.
To evaluate outcomes for men with biochemically recurrent prostate cancer who were selected for transponder-guided salvage radiotherapy (SRT) to the prostate bed alone by Ga-labelled prostate-specific membrane antigen positron emission tomography (Ga-PSMA-PET).
This is a single-arm, prospective study of men with a prostate-specific antigen (PSA) level rising to 0.1-2.5 ng/mL following radical prostatectomy. Patients were staged with Ga-PSMA-PET and those with a negative finding, or a positive finding localised to the prostate bed, continued to SRT only to the prostate bed alone with real-time target-tracking using electromagnetic transponders. The primary endpoint was freedom from biochemical relapse (FFBR, PSA > 0.2 ng/mL from the post-radiotherapy nadir). Secondary endpoints were time to biochemical relapse, toxicity and patient-reported quality of life (QoL).
Ninety-two patients (median PSA of 0.18 ng/ml, IQR 0.12-0.36), were screened with Ga-PSMA-PET and metastatic disease was found in 20 (21.7%) patients. Sixty-nine of 72 non-metastatic patients elected to proceed with SRT. At the interim (3-year) analysis, 32 (46.4%) patients (95% CI 34.3-58.8%) were FFBR. The median time to biochemical relapse was 16.1 months. The rate of FFBR was 82.4% for ISUP grade-group 2 patients. Rates of grade 2 or higher gastrointestinal and genitourinary toxicity were 0% and 15.2%, respectively. General health and disease-specific QoL remained stable.
Pre-SRT Ga-PSMA-PET scans detect metastatic disease in a proportion of patients at low PSA levels but fail to improve FFBR. Transponder-guided SRT to the prostate bed alone is associated with a favourable toxicity profile and preserved QoL.
ACTRN12615001183572, 03/11/2015, retrospectively registered.
评估通过 Ga 标记前列腺特异性膜抗原正电子发射断层扫描(Ga-PSMA-PET)选择行放射性前列腺切除术床内转移灶引导的挽救性放疗(SRT)的生化复发前列腺癌患者的结局。
这是一项针对 PSA 水平在前列腺切除术治疗后上升至 0.1-2.5ng/mL 的患者的单臂、前瞻性研究。患者通过 Ga-PSMA-PET 进行分期,对于无转移灶或转移灶局限于前列腺床的患者,仅对前列腺床行 SRT,同时使用电磁感应器实时追踪目标。主要终点为生化无复发生存率(PSA 从放疗后最低点升高至>0.2ng/mL 的患者比例)。次要终点为生化复发时间、毒性和患者报告的生活质量(QoL)。
92 名患者(中位 PSA 为 0.18ng/ml,IQR 为 0.12-0.36)进行了 Ga-PSMA-PET 筛查,其中 20 名(21.7%)患者发现了转移灶。72 名非转移性患者中有 69 名选择行 SRT。在中期(3 年)分析中,32 名(46.4%)患者(95%CI 34.3-58.8%)达到生化无复发生存率。生化复发的中位时间为 16.1 个月。ISUP 分级组 2 患者的生化无复发生存率为 82.4%。2 级或更高级别的胃肠道和泌尿生殖系统毒性的发生率分别为 0%和 15.2%。一般健康状况和疾病特异性 QoL 保持稳定。
SRT 前的 Ga-PSMA-PET 扫描可在 PSA 水平较低的患者中检测出一部分转移灶,但未能提高生化无复发生存率。仅对前列腺床行放射性前列腺切除术床内转移灶引导的 SRT 具有良好的毒性特征和保留 QoL。
ACTRN12615001183572,于 2015 年 3 月 11 日注册,为回顾性注册。