Radiotherapy Unit, Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy.
CyberKnife Center, Istituto Fiorentino di Cura ed Assistenza, Florence, Italy.
Clin Oncol (R Coll Radiol). 2018 Feb;30(2):93-100. doi: 10.1016/j.clon.2017.11.007. Epub 2017 Dec 6.
Robotic stereotactic body radiotherapy (rSBRT) to local recurrences emerged as a valuable option for exclusive local failure after prior external beam radiation therapy (EBRT) for localised prostate cancer. The aim of this study was to assess the efficacy and safety of rSBRT in patients experiencing locally recurrent prostate cancer after prior definitive or postoperative radiotherapy using the Cyberknife.
Data from 50 patients were retrospectively reviewed. Local recurrence was assessed by 18F-choline positron emission tomography and pelvic magnetic resonance imaging; a dose of 30 Gy was delivered in five fractions. Prostate-specific antigen (PSA) was assessed at 2 months, 6 months and every 4 months thereafter. Toxicity was assessed according to CTCAE v.4.03.
All patients received prior EBRT. The median EQD2 total dose was 74 Gy (60-80 Gy). Eleven patients were receiving androgen deprivation after prior biochemical failure. At 6 months, 41 patients showed a median PSA decline of -77.1% (14.3-99.3%), whereas nine patients experienced a median PSA elevation of +58.7% (0-2300.0%). Biochemical relapse-free survival (BRFS) was 80.0%. Impaired BRFS was correlated with the high-risk category at diagnosis (P = 0.014, hazard ratio 5.61) and ongoing androgen deprivation (P = 0.025, hazard ratio 2.98). Neither clinical variables nor dosimetric parameters were found to be predictive for toxicity.
Focal rSBRT can achieve durable remission in locally relapsing patients and systemic treatment can be postponed with acceptable toxicity. Accurate patient selection is mandatory to maximise disease control.
机器人立体定向体放射治疗(rSBRT)作为局部前列腺癌根治性或术后放疗后局部复发的一种有价值的选择,已成为一种有价值的选择。本研究的目的是评估使用 Cyberknife 对局部复发前列腺癌患者进行 rSBRT 的疗效和安全性。
回顾性分析 50 例患者的数据。通过 18F-胆碱正电子发射断层扫描和盆腔磁共振成像评估局部复发;给予 30Gy 剂量,分 5 次给予。前列腺特异性抗原(PSA)在 2 个月、6 个月和此后每 4 个月评估一次。毒性根据 CTCAE v.4.03 进行评估。
所有患者均接受过 EBRT 治疗。中位 EQD2 总剂量为 74Gy(60-80Gy)。11 例患者在生化失败后接受雄激素剥夺治疗。6 个月时,41 例患者 PSA 中位数下降 77.1%(14.3-99.3%),9 例患者 PSA 中位数升高 58.7%(0-2300.0%)。生化无复发生存(BRFS)为 80.0%。BRFS 受损与诊断时的高危类别(P=0.014,风险比 5.61)和持续雄激素剥夺(P=0.025,风险比 2.98)相关。临床变量和剂量学参数均不能预测毒性。
局部 rSBRT 可使局部复发患者获得持久缓解,且毒性可接受时可推迟全身治疗。为了最大限度地控制疾病,必须对患者进行准确选择。