Academic Department of Radiation Oncology, Centre Oscar Lambret, Lille, France; CRIStAL UMR CNRS 9189, Lille University, Lille, France.
Academic Department of Radiation Oncology, Centre Oscar Lambret, Lille, France.
Int J Radiat Oncol Biol Phys. 2019 Nov 15;105(4):727-734. doi: 10.1016/j.ijrobp.2019.07.012. Epub 2019 Jul 22.
To assess the efficacy and safety of salvage stereotactic body radiation therapy (SBRT) in patients with biopsy-proven local prostate cancer recurrence after radiation therapy.
Between April 2010 and January 2017, 100 patients were included in 7 centers. Disease extension was assessed by pelvic multiparametric magnetic resonance imaging and choline positron emission tomography in 87% and 94% of patients, respectively. The median time interval between the 2 treatments was 7.5 years (range, 2-18). Median prostate-specific antigen at recurrence was 4.3 ng/mL (range, 2-38). Median SBRT dose was 36 Gy (range, 25-36.25) in 6 fractions (range, 5-6), every other day. Thirty-four percent of patients were treated by androgen deprivation therapy for a median duration of 12 months. Toxicity was assessed according to Common Terminology Criteria for Adverse Events version 4.03.
Median follow-up was 29.3 months (range, 4-91). Second biochemical recurrence-free survival rate at 3 years was 55% (95% confidence interval [CI], 42%-66%). The initial D'Amico group, time interval after first radiation therapy, and SBRT dose were prognostic factors of biochemical recurrence-free survival in multivariate analysis (P = .09, P = .025, P = .018, respectively). No patient developed acute gastrointestinal toxicity of grade >1; rates of acute genitourinary toxicity of grade 2 and 3 were 8% and 1%, respectively. The actuarial 3-year grade ≥2 genitourinary and gastrointestinal toxicity was 20.8% (95% CI, 13%-29%) and 1% (95% CI, 0.1%-5.1%), respectively. One patient presented with neuritis of grade 3.
With a short follow-up, this study shows that salvage SBRT allows for encouraging control and acceptable toxicity. Further prospective studies are necessary to confirm these preliminary results and to determine late toxicity.
评估挽救性立体定向体放射治疗(SBRT)在放射治疗后经活检证实局部前列腺癌复发患者中的疗效和安全性。
在 2010 年 4 月至 2017 年 1 月期间,有 100 名患者被纳入 7 个中心进行研究。87%和 94%的患者分别通过盆腔多参数磁共振成像和胆碱正电子发射断层扫描评估疾病的扩展情况。两种治疗之间的中位时间间隔为 7.5 年(范围,2-18 年)。复发时中位前列腺特异性抗原为 4.3ng/ml(范围,2-38ng/ml)。SBRT 中位剂量为 36Gy(范围,25-36.25Gy),分 6 次(范围,5-6 次),隔天一次。34%的患者接受了中位持续时间为 12 个月的雄激素剥夺治疗。毒性根据 4.03 版通用不良事件术语标准进行评估。
中位随访时间为 29.3 个月(范围,4-91 个月)。3 年时第二次生化无复发生存率为 55%(95%置信区间[CI],42%-66%)。在多因素分析中,初始 D'Amico 组、首次放射治疗后时间间隔和 SBRT 剂量是生化无复发生存的预后因素(P=.09,P=.025,P=.018)。没有患者出现 1 级以上的急性胃肠道毒性;急性泌尿生殖系统毒性 2 级和 3 级的发生率分别为 8%和 1%。3 年时,累积发生率为 20.8%(95%CI,13%-29%)和 1%(95%CI,0.1%-5.1%)的≥2 级泌尿生殖系统和胃肠道毒性。1 例患者出现 3 级神经炎。
在随访时间较短的情况下,本研究表明挽救性 SBRT 可获得令人鼓舞的控制效果,且毒性可接受。需要进一步的前瞻性研究来证实这些初步结果,并确定晚期毒性。