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前列腺床加速亚分次放射治疗的前瞻性 1/2 期研究的 5 年结果。

5-Year Outcomes of a Prospective Phase 1/2 Study of Accelerated Hypofractionated Radiation Therapy to the Prostate Bed.

机构信息

Department of Radiation Oncology, Sunnybrook Health Sciences Centre, University of Toronto.

Clinical Trials, Odette Cancer Centre, Sunnybrook Health Sciences Centre.

出版信息

Pract Radiat Oncol. 2019 Sep-Oct;9(5):354-361. doi: 10.1016/j.prro.2019.04.010. Epub 2019 May 16.

Abstract

PURPOSE

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.

METHODS AND MATERIALS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法和材料

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。

结果

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。

结论

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。

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