Kunogi Hiroaki, Wakumoto Yoshiaki, Kawamoto Terufumi, Oshima Masaki, Horie Shigeo, Sasai Keisuke
Department of Radiation Oncology, Juntendo University, Tokyo, Japan.
Department of Urology, Juntendo University, Tokyo, Japan.
J Contemp Brachytherapy. 2020 Dec;12(6):554-561. doi: 10.5114/jcb.2020.101688. Epub 2020 Dec 16.
To prospectively investigate the efficacy and feasibility of focal low-dose-rate (LDR) prostate brachytherapy for low- and intermediate-risk prostate cancer.
Between October 2014 and May 2019, nineteen low- and intermediate-risk prostate cancer patients who presented with abnormality on both diffusion-weighted and T2-weighted magnetic resonance imaging (MRI) underwent focal LDR brachytherapy at our institution. Focal gross tumor volume (F-GTV) was delineated on transrectal ultrasound, based on abnormality seen on fused T2-weighted MRI. F-GTV was expanded by 5 mm, as a safety margin, to create focal clinical target volume (F-CTV). Prescribed dose to F-CTV was 145 Gy. Biochemical recurrence (BCR) was determined using Phoenix criterion (prostate specific antigen nadir + 2 ng/ml). Pre- and post-implant dosimetry data were compared using non-parametric Wilcoxon's rank sum test. Treatment-related toxicities were evaluated using common terminology criteria for adverse events.
Mean F-CTV D was significantly lower in the post-implant evaluation than in intraoperative planning ( = 0.004). On post-implant dosimetry, the mean D for F-GTV and mean V for the entire prostate were 222 Gy and 35%, respectively. Median follow-up time for all patients was 31 months. BCR occurred in one patient after 23 months. Kaplan-Meier 2-year BCR-free rate was 92.9% (95% confidence interval [CI]: 79.4-100%). No patients had grade 1 or greater gastrointestinal toxicity. Three patients who were taking αblockers to treat benign prostatic hyperplasia (present before brachytherapy), experienced no treatment-related genitourinary toxicities. Two patients suffered from temporary grade 2 urinary frequency. None of the remaining patients experienced grade 2 or higher genitourinary toxicity.
Focal LDR prostate brachytherapy appears acceptable for MRI-based index tumors, with a low cumulative incidence of BCR. Such brachytherapy might offer a feasible minimally invasive therapeutic option for localized prostate cancer.
前瞻性研究聚焦低剂量率(LDR)前列腺近距离放射治疗对低危和中危前列腺癌的疗效及可行性。
2014年10月至2019年5月,19例在扩散加权和T2加权磁共振成像(MRI)上均表现异常的低危和中危前列腺癌患者在我院接受了聚焦LDR近距离放射治疗。基于融合的T2加权MRI上所见的异常,在经直肠超声上勾画聚焦大体肿瘤体积(F-GTV)。F-GTV扩大5 mm作为安全边界,以创建聚焦临床靶体积(F-CTV)。F-CTV的处方剂量为145 Gy。使用Phoenix标准(前列腺特异性抗原最低点+2 ng/ml)确定生化复发(BCR)。使用非参数Wilcoxon秩和检验比较植入前和植入后的剂量学数据。使用不良事件通用术语标准评估治疗相关毒性。
植入后评估中F-CTV的平均D值显著低于术中计划(P = 0.004)。在植入后剂量学中,F-GTV的平均D值和整个前列腺的平均V值分别为222 Gy和35%。所有患者的中位随访时间为31个月。1例患者在23个月后发生BCR。Kaplan-Meier 2年无BCR率为92.9%(95%置信区间[CI]:79.4 - 100%)。无患者发生1级或更高级别的胃肠道毒性。3例正在服用α受体阻滞剂治疗良性前列腺增生(近距离放射治疗前存在)的患者未出现治疗相关的泌尿生殖系统毒性。2例患者出现暂时性2级尿频。其余患者均未出现2级或更高级别的泌尿生殖系统毒性。
聚焦LDR前列腺近距离放射治疗对于基于MRI的索引肿瘤似乎是可接受的,BCR累积发生率较低。这种近距离放射治疗可能为局限性前列腺癌提供一种可行的微创治疗选择。