Department of Radiation Oncology, Odette Cancer Centre, University of Toronto, Toronto, Canada.
Int J Radiat Oncol Biol Phys. 2010 Jul 1;77(3):811-7. doi: 10.1016/j.ijrobp.2009.05.054. Epub 2009 Oct 14.
To determine the short- and medium-term effects of a single high-dose-rate brachytherapy fraction of 15 Gy and hypofractionated external beam radiation therapy for prostate cancer.
Eligible patients had localized prostate cancer with a Gleason score of 7 and a prostate-specific antigen (PSA) concentration of <20 ng/ml or a Gleason score of 6 with a PSA concentration of 10 to 20 ng/ml. Patients received high-dose-rate brachytherapy as a single 15-Gy dose, followed by external beam radiation therapy at 37.5 Gy in 15 fractions, and were followed prospectively for toxicity (using Common Terminology Criteria for Adverse Events version 3.0), urinary symptoms (using the International Prostate Symptom Score [IPSS]), erectile function (with the International Index of Erectile Function [IIEF]), and health-related quality of life (with the Expanded Prostate Cancer Index Composite [EPIC]). Clinical examinations and PSA measurements were performed at every visit, and prostate biopsies were repeated at 2 years. The trial accrued 125 patients, with a median follow-up of 1.14 years.
Acute grade 2 and 3 genitourinary toxicity occurred in 62% and 1.6% of patients, respectively, and acute grade 2 gastrointestinal toxicity occurred in 6.5% of patients. No grade 3 late toxicity has occurred: 47% of patients had grade 2 genitourinary and 10% of patients had grade 2 gastrointestinal toxicity. Median IPSSs rose from 5 at baseline to 12 at 1 month and returned to 7 at 3 months. Of the total number of patients who were initially potent (IIEF, >21), 8% of patients developed mild to moderate dysfunction, and 27% of patients developed severe erectile dysfunction. Baseline EPIC bowel, urinary, and sexual bother scores decreased by 9, 7, and 19 points, respectively, at 1 year. No patient has experienced biochemical failure, and 16 of the first 17 biopsy results showed no malignancy.
Treatment is well tolerated in the short and medium term, with low toxicity and encouraging early indicators of disease control.
确定单次高剂量率近距离治疗 15Gy 与外照射分割治疗局限性前列腺癌的短期和中期疗效。
符合条件的患者为局限性前列腺癌,Gleason 评分为 7 分且 PSA 浓度<20ng/ml,或 Gleason 评分为 6 分且 PSA 浓度为 10-20ng/ml。患者接受高剂量率近距离治疗,单次 15Gy 剂量,随后进行 37.5Gy/15 次的外照射治疗,并进行前瞻性随访以评估毒性(采用不良事件通用术语标准 3.0 版)、尿症状(采用国际前列腺症状评分[IPSS])、勃起功能(采用国际勃起功能指数[IIEF])和健康相关生活质量(采用前列腺癌指数综合量表[EPIC])。每次就诊时进行临床检查和 PSA 测量,并在第 2 年重复进行前列腺活检。该试验共入组 125 例患者,中位随访时间为 1.14 年。
急性 2 级和 3 级泌尿生殖系统毒性发生率分别为 62%和 1.6%,急性 2 级胃肠道毒性发生率为 6.5%。无 3 级晚期毒性:47%的患者出现 2 级泌尿生殖系统毒性,10%的患者出现 2 级胃肠道毒性。中位 IPSS 从基线时的 5 分升高至 1 个月时的 12 分,3 个月时恢复至 7 分。最初勃起功能正常(IIEF>21)的患者中,8%的患者出现轻度至中度性功能障碍,27%的患者出现严重勃起功能障碍。基线时 EPIC 肠、尿和性功能困扰评分分别下降 9、7 和 19 分,1 年后下降更为明显。无患者发生生化失败,17 例活检中有 16 例结果未见恶性肿瘤。
短期和中期治疗耐受性良好,毒性低,早期疾病控制效果令人鼓舞。