Jensen Lindsay, Yuh Bertram, Wong Jeffrey Y C, Schultheiss Timothy, Cheng Jonathan, Ruel Nora, Twardowski Przemyslaw, Sampath Sagus
Department of Radiation Oncology, City of Hope National Medical Center, Duarte, California.
Department of Urology, City of Hope National Medical Center, Duarte, California.
Adv Radiat Oncol. 2017 Aug 8;2(4):597-607. doi: 10.1016/j.adro.2017.08.004. eCollection 2017 Oct-Dec.
There are limited long-term data on patients treated with image guided intensity modulated radiation therapy (IG-IMRT) for prostate cancer recurrence or high-risk disease features after radical prostatectomy. We report single-institution results for patients treated with IG-IMRT and identify variables associated with outcome.
This is a retrospective chart review consisting of 313 consecutive patients who were treated with adjuvant or salvage IG-IMRT from 2004 to 2013. Cox proportional hazards analysis was used to identify factors related to survival and toxicity. Toxicity was graded using the Common Terminology Criteria for Adverse Events Version 4.0.
The median follow-up was 55 months (range, 6-131 months). The median pre-radiation therapy (RT) prostate-specific antigen (PSA) was 0.3 ng/mL (range, <0.01-55.4). The vast majority of patients (87%) received elective pelvic nodal irradiation (median dose: 45 Gy). Androgen deprivation therapy (ADT) was given to 39% of patients for a median of 9 months. Five-year biochemical progression-free survival and distant metastasis-free survival were 59% (95% confidence interval, 53%-66%) and 89% (95% confidence interval, 85%-93%), respectively. On multivariate analysis, higher pre-RT PSA (>0.2 ng/mL), biopsy Gleason score (≥7 [4+3]), and duration of ADT (>6 months) were significantly associated ( < .05) with biochemical progression-free survival. Actuarial late grade 3 genitourinary and gastrointestinal toxicities at 5 years were 10% and 2%, respectively.
Our results suggest that lower pre-RT PSA level and longer duration of ADT are associated with improved biochemical control. The incidence of late grade 3 gastrointestinal toxicity was low, but late grade 3 genitourinary toxicity was higher than anticipated.
关于接受图像引导调强放射治疗(IG-IMRT)治疗前列腺癌根治术后复发或高危疾病特征患者的长期数据有限。我们报告单机构接受IG-IMRT治疗患者的结果,并确定与预后相关的变量。
这是一项回顾性病历审查,包括2004年至2013年连续接受辅助或挽救性IG-IMRT治疗的313例患者。采用Cox比例风险分析确定与生存和毒性相关的因素。使用不良事件通用术语标准第4.0版对毒性进行分级。
中位随访时间为55个月(范围6-131个月)。放疗前(RT)前列腺特异性抗原(PSA)的中位数为0.3 ng/mL(范围<0.01-55.4)。绝大多数患者(87%)接受了选择性盆腔淋巴结照射(中位剂量:45 Gy)。39%的患者接受了雄激素剥夺治疗(ADT),中位时间为9个月。5年生化无进展生存率和远处转移无进展生存率分别为59%(95%置信区间,53%-66%)和89%(95%置信区间,85%-93%)。多因素分析显示,放疗前PSA水平较高(>0.2 ng/mL)、活检Gleason评分(≥7[4+3])和ADT持续时间(>6个月)与生化无进展生存显著相关(P<0.05)。5年精算3级晚期泌尿生殖系统和胃肠道毒性分别为10%和2%。
我们的结果表明,放疗前PSA水平较低和ADT持续时间较长与改善生化控制相关。3级晚期胃肠道毒性发生率较低,但3级晚期泌尿生殖系统毒性高于预期。