Servei de Radio-oncologia, Institut Oncològic Teknon, Vilana 12, 08022 Barcelona-E, Spain.
Technol Cancer Res Treat. 2010 Oct;9(5):509-14. doi: 10.1177/153303461000900509.
The purpose of this study is to report toxicity and outcome results in patients with gynaecological tumours treated with a final boost using extra-cranial stereotactic radiotherapy (SRT) with a linac-based micro-multileaf collimator technique as an alternative to high-dose rate brachytherapy (HDR-BT). Since January 2002, 26 patients with either endometrial (n = 17) or cervical (n = 9) cancer were treated according to this protocol: 45-50.4 Gy external radiotherapy (RT) to the pelvic +/- para-aortic regions followed by a final SRT boost of 2 x 7 Gy to the vaginal vault (4-7 day interval between fractions). Median age was 62 years (37-74 range). Fifteen patients were diagnosed with adenocarcinoma, 7 with squamous-cell carcinoma, and 4 with sarcoma. FIGO stage I (n = 17), stage II (n = 7), and stage III (n = 2). Toxicity was scored according to RTOG/EORTC criteria. No severe (> grade-3) acute urinary or low-gastrointestinal (GI) toxicity was observed during treatment and up to 3 months after treatment completion. Moderate (grade < or = 3) acute urinary or low-GI toxicity was observed in 23% and 35% of patients, respectively. After a median follow-up of 47 months (4-77, range), late urinary, low-GI, and sexual > or = grade-2 (worst score) has been reported in 4%, 12% and 29.4% of patients, respectively. The 3-year loco-regional failure-free and overall survival rates were 96% and 95%, respectively. Preliminary results on feasibility, tolerance, and outcome with SRT are encouraging and may be considered a sound alternative to HDR-BT for gynecologic tumors.
本研究旨在报告采用外颅立体定向放射治疗(SRT)联合基于直线加速器的微多叶准直器技术对妇科肿瘤患者进行最终加量的毒性和结果。自 2002 年 1 月以来,26 例子宫内膜(n=17)或宫颈(n=9)癌患者按照该方案治疗:盆腔 +/- 腹主动脉旁区域给予 45-50.4Gy 外照射(RT),随后阴道穹窿给予 2x7Gy 的最终 SRT 加量(分次间隔 4-7 天)。中位年龄为 62 岁(37-74 岁)。15 例患者诊断为腺癌,7 例为鳞状细胞癌,4 例为肉瘤。FIGO 分期为 I 期(n=17)、II 期(n=7)和 III 期(n=2)。毒性根据 RTOG/EORTC 标准评分。在治疗期间和治疗结束后 3 个月内,没有观察到严重(> 3 级)急性尿毒性或低胃肠道(GI)毒性。分别有 23%和 35%的患者观察到中度(< 或 = 3 级)急性尿毒性或低 GI 毒性。中位随访 47 个月(4-77 个月,范围)后,分别有 4%、12%和 29.4%的患者出现迟发性尿、低 GI 和>或= 2 级(最差评分)的生殖毒性。3 年局部区域无失败生存率和总生存率分别为 96%和 95%。SRT 的可行性、耐受性和结果的初步结果令人鼓舞,可被认为是妇科肿瘤患者进行 HDR-BT 的一种合理替代方法。