Department of Radiation Medicine, Georgetown University Hospital, Washington, DC 20007, USA.
Radiat Oncol. 2013 Mar 13;8:58. doi: 10.1186/1748-717X-8-58.
Stereotactic body radiation therapy (SBRT) delivers fewer high-dose fractions of radiation which may be radiobiologically favorable to conventional low-dose fractions commonly used for prostate cancer radiotherapy. We report our early experience using SBRT for localized prostate cancer.
Patients treated with SBRT from June 2008 to May 2010 at Georgetown University Hospital for localized prostate carcinoma, with or without the use of androgen deprivation therapy (ADT), were included in this retrospective review of data that was prospectively collected in an institutional database. Treatment was delivered using the CyberKnife® with doses of 35 Gy or 36.25 Gy in 5 fractions. Biochemical control was assessed using the Phoenix definition. Toxicities were recorded and scored using the CTCAE v.3. Quality of life was assessed before and after treatment using the Short Form-12 Health Survey (SF-12), the American Urological Association Symptom Score (AUA) and Sexual Health Inventory for Men (SHIM) questionnaires. Late urinary symptom flare was defined as an AUA score ≥ 15 with an increase of ≥ 5 points above baseline six months after the completion of SBRT.
One hundred patients (37 low-, 55 intermediate- and 8 high-risk according to the D'Amico classification) at a median age of 69 years (range, 48-90 years) received SBRT, with 11 patients receiving ADT. The median pre-treatment prostate-specific antigen (PSA) was 6.2 ng/ml (range, 1.9-31.6 ng/ml) and the median follow-up was 2.3 years (range, 1.4-3.5 years). At 2 years, median PSA decreased to 0.49 ng/ml (range, 0.1-1.9 ng/ml). Benign PSA bounce occurred in 31% of patients. There was one biochemical failure in a high-risk patient, yielding a two-year actuarial biochemical relapse free survival of 99%. The 2-year actuarial incidence rates of GI and GU toxicity ≥ grade 2 were 1% and 31%, respectively. A median baseline AUA symptom score of 8 significantly increased to 11 at 1 month (p=0.001), however returned to baseline at 3 months (p=0.60). Twenty one percent of patients experienced a late transient urinary symptom flare in the first two years following treatment. Of patients who were sexually potent prior to treatment, 79% maintained potency at 2 years post-treatment.
SBRT for clinically localized prostate cancer was well tolerated, with an early biochemical response similar to other radiation therapy treatments. Benign PSA bounces were common. Late GI and GU toxicity rates were comparable to conventionally fractionated radiation therapy and brachytherapy. Late urinary symptom flares were observed but the majority resolved with conservative management. A high percentage of men who were potent prior to treatment remained potent two years following treatment.
立体定向体部放射治疗(SBRT)采用较少的高剂量分次照射,这可能在放射生物学上有利于常规低剂量分次照射,常用于前列腺癌放射治疗。我们报告使用 SBRT 治疗局限性前列腺癌的早期经验。
回顾性分析 2008 年 6 月至 2010 年 5 月期间在乔治敦大学医院接受 SBRT 治疗的局限性前列腺癌患者的数据,这些患者接受或未接受雄激素剥夺治疗(ADT)。这些数据是在一个机构数据库中前瞻性收集的。使用 CyberKnife®治疗,剂量为 35 Gy 或 36.25 Gy,分 5 次。采用 Phoenix 定义评估生化控制情况。使用 CTCAE v.3 记录和评分毒性。使用短期表单-12 健康调查(SF-12)、美国泌尿协会症状评分(AUA)和男性性功能健康问卷(SHIM)在治疗前后评估生活质量。晚期尿症状发作定义为 SBRT 完成后 6 个月时 AUA 评分≥15,与基线相比增加≥5 分。
100 例患者(37 例低危、55 例中危和 8 例高危,根据 D'Amico 分类),中位年龄 69 岁(范围,48-90 岁),接受 SBRT 治疗,11 例患者接受 ADT。中位治疗前前列腺特异性抗原(PSA)为 6.2ng/ml(范围,1.9-31.6ng/ml),中位随访时间为 2.3 年(范围,1.4-3.5 年)。2 年时,中位 PSA 降至 0.49ng/ml(范围,0.1-1.9ng/ml)。31%的患者出现良性 PSA 反弹。高危患者中有 1 例生化失败,2 年生化无复发生存率为 99%。2 年时 GI 和 GU 毒性≥2 级的发生率分别为 1%和 31%。基线时 AUA 症状评分中位数为 8 分,1 个月时显著增加至 11 分(p=0.001),但在 3 个月时恢复至基线(p=0.60)。治疗后 2 年内,21%的患者出现短暂的晚期尿症状发作。治疗前有性功能的患者中,79%在治疗后 2 年仍保持性功能。
SBRT 治疗临床局限性前列腺癌患者耐受性良好,生化反应与其他放射治疗相似。良性 PSA 反弹很常见。晚期 GI 和 GU 毒性发生率与常规分割放疗和近距离放疗相当。观察到晚期尿症状发作,但大多数通过保守治疗缓解。治疗前有性功能的男性中,有很高比例的患者在治疗后 2 年内仍保持性功能。