Instituto do Câncer do Estado de São Paulo, Universidade de São Paulo, São Paulo, Brazil.
Instituto do Câncer do Estado de São Paulo, Universidade de São Paulo, São Paulo, Brazil.
Int J Radiat Oncol Biol Phys. 2021 Apr 1;109(5):1263-1270. doi: 10.1016/j.ijrobp.2020.12.020. Epub 2020 Dec 17.
Postoperative radiation therapy (RT) is a common therapy used for patients with prostate cancer. Although clinical trials have established the safety and efficacy of hypofractionation as a primary therapy, there are limited data in a postoperative setting. We conducted a prospective trial to evaluate the safety and feasibility of postoperative hypofractionated RT to the prostate bed.
In this phase 2 trial, patients submitted to radical prostatectomy were treated with hypofractionated RT to the prostate bed (adjuvant or salvage). The prescribed dose was 51 Gy in 15 fractions (3.4 Gy per fraction), using intensity modulated and image guided radiation therapy techniques. The primary endpoint was the rate of acute genitourinary (GU) grade ≥2 toxicity. Secondary endpoints included acute gastrointestinal (GI) and late GU/GI toxicities, biochemical failure-free survival (BFFS), metastasis-free survival, cancer-specific survival, overall survival, and health-related quality of life.
Of 64 enrolled patients, 61 received radiation therapy (57 salvage and 4 adjuvant radiation therapy). After a median follow-up of 16 months, 11.5% of patients experienced acute grade ≥2 GU symptoms and 13.1% experienced acute grade ≥2 GI symptoms. The late grade ≥2 GU toxicity rate was 8.2%, and 1 patient (1.6%) developed both acute and late grade 3 GU toxicity. The late grade ≥2 GI toxicity rate was 11.5%, and no grade 3 GI adverse events were reported. The short follow-up limits our ability to perform a robust oncologic endpoint assessment; however, the 2-year BFFS, use of subsequent salvage therapy, and the development of metastasis were 95.1%, 0%, and 0%, respectively.
Hypofractionated RT to the prostate bed in 15 treatments was safe, with an acceptable GU and GI toxicity profile. Further study in large, randomized trials is warranted.
术后放疗(RT)是治疗前列腺癌患者的常用方法。虽然临床试验已经证实了分割剂量放疗作为主要治疗方法的安全性和有效性,但在术后环境中数据有限。我们进行了一项前瞻性试验,以评估前列腺床术后分割剂量放疗的安全性和可行性。
在这项 2 期试验中,接受根治性前列腺切除术的患者接受前列腺床的分割剂量放疗(辅助或挽救性放疗)。处方剂量为 51Gy,分 15 次(每次 3.4Gy),使用强度调制和图像引导放疗技术。主要终点是急性泌尿生殖系统(GU)≥2 级毒性的发生率。次要终点包括急性胃肠道(GI)和晚期 GU/GI 毒性、生化无失败生存(BFFS)、无转移生存、癌症特异性生存、总生存和健康相关生活质量。
在 64 名入组患者中,61 名患者接受了放疗(57 例挽救性放疗和 4 例辅助性放疗)。中位随访 16 个月后,11.5%的患者出现急性 GU 症状≥2 级,13.1%的患者出现急性 GI 症状≥2 级。晚期 GU 毒性≥2 级的发生率为 8.2%,1 例(1.6%)患者同时出现急性和晚期 3 级 GU 毒性。晚期 GI 毒性≥2 级的发生率为 11.5%,无 3 级 GI 不良事件报告。随访时间短限制了我们进行稳健的肿瘤学终点评估的能力;然而,2 年 BFFS、随后挽救性治疗的使用和转移的发展分别为 95.1%、0%和 0%。
15 次治疗的前列腺床分割剂量放疗是安全的,具有可接受的 GU 和 GI 毒性特征。需要在大型随机试验中进一步研究。