Department of Radiation Oncology, Sunnybrook Health Sciences Centre, University of Toronto.
Clinical Trials, Odette Cancer Centre, Sunnybrook Health Sciences Centre.
Pract Radiat Oncol. 2019 Sep-Oct;9(5):354-361. doi: 10.1016/j.prro.2019.04.010. Epub 2019 May 16.
To report the 5-year outcomes from a single institution, prospective, phase 1/2 study on hypofractionated, accelerated radiation therapy to the prostate bed after radical prostatectomy.
Patients enrolled in this study were all eligible for postoperative radiation therapy and received a prescribed dose of 51 Gy in 17 fractions to the prostate bed. On follow-up, gastrointestinal (GI) and genitourinary (GU) toxicity was assessed using the National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0; prostate-specific antigen (PSA) was evaluated and quality of life was assessed using the Expanded Prostate Cancer Index Composite (EPIC) questionnaire.
A total of 30 patients were enrolled between 2008 and 2011. Median age was 65 (52-75) years. Median pretreatment PSA was 0.12 ng/mL (0.01-1.42). Twenty-six (93%) patients had Gleason ≤7 disease, 13 (43%) had pT3 disease, and 20 (67%) had positive margins. Twenty-six patients (87%) underwent radiation therapy as salvage treatment. After a median follow-up of 6.4 (2.1-8.1) years, no patient experienced Common Terminology Criteria for Adverse Events grade 3/4 toxicity. Eleven patients (37%) had grade 2 genitourinary and 2 (7%) had grade 2 gastrointestinal toxicity. At baseline and 5 years after radiation therapy, mean EPIC urinary domain score was 80% (standard deviation, 18%) and 82% (17%). Mean EPIC bowel domain score was 93% (13%) and 93% (15%). One patient (4%) had a minimally clinically important change in urinary domain score and 1 patient (4%) had a minimally clinically important change in bowel domain score. Nelson-Aalen estimated cumulative incidence of biochemical failure was 31% (nadir +0.2) and 18% (nadir +2.0) at 5 years. Four-year PSA ≥0.4 was predictive of subsequent androgen deprivation therapy use (Nelson-Aalen cumulative incidence: 1.45; P < .0001). Five patients (17%) received hormonal therapy for biochemical failure. Nelson-Aalen estimated cumulative incidence of hormone therapy use was 14% at 5 years. All patients who received hormone therapy had PSA >0.4 at 4 years.
In this phase 1/2 study, hypofractionated postoperative radiation therapy seems to have good clinical efficacy without significant late toxicity. Phase 3 studies are warranted.
报告单中心前瞻性 1/2 期研究中,前列腺根治术后前列腺床接受低分割加速放疗的 5 年结果。
入组本研究的患者均符合术后放疗条件,给予前列腺床 51 Gy/17 次的处方剂量。随访时,使用国家癌症研究所不良事件通用术语标准 3.0 评估胃肠道(GI)和泌尿生殖系统(GU)毒性;使用前列腺癌指数综合问卷(EPIC)评估前列腺特异性抗原(PSA)并评估生活质量。
2008 年至 2011 年期间共入组 30 例患者。中位年龄为 65 岁(52-75 岁)。中位预处理 PSA 为 0.12ng/mL(0.01-1.42)。26 例(93%)患者 Gleason 评分≤7,13 例(43%)患者 pT3 期,20 例(67%)患者切缘阳性。26 例(87%)患者接受挽救性放疗。中位随访 6.4 年后(2.1-8.1 年),无患者出现 3/4 级不良事件。11 例(37%)患者出现 2 级泌尿生殖系统毒性,2 例(7%)患者出现 2 级胃肠道毒性。放疗后基线和 5 年时,EPIC 尿域评分分别为 80%(标准差 18%)和 82%(17%)。EPIC 肠域评分分别为 93%(13%)和 93%(15%)。1 例(4%)患者尿域评分出现临床意义最小变化,1 例(4%)患者肠域评分出现临床意义最小变化。Nelson-Aalen 估计生化失败的累积发生率为 31%(最低点+0.2)和 18%(最低点+2.0),分别在 5 年时和最低点+2.0)。4 年 PSA≥0.4 可预测随后使用雄激素剥夺治疗(Nelson-Aalen 累积发生率:1.45;P<0.0001)。5 例(17%)患者因生化失败接受激素治疗。Nelson-Aalen 估计 5 年时激素治疗的累积发生率为 14%。所有接受激素治疗的患者在 4 年内 PSA>0.4。
在这项 1/2 期研究中,前列腺根治术后低分割加速放疗似乎具有良好的临床疗效,且无明显晚期毒性。需要进行 3 期研究。