Vera Robyn, Trombetta Mark, Mukhopadhyay Nitai D, Packard Matthew, Arthur Douglas
Department of Radiation Oncology, Virginia Commonwealth University, Richmond, Virginia.
Department of Radiation Oncology, Allegheny General Hospital, Pittsburgh, Pennsylvania.
Pract Radiat Oncol. 2014 May-Jun;4(3):147-152. doi: 10.1016/j.prro.2013.07.004. Epub 2013 Aug 15.
To evaluate cosmesis and toxicity in early-stage breast cancer patients treated with adjuvant 3D-CRT who received accelerated partial breast irradiation (APBI).
From November 2003 to June 2006, 60 breasts on 59 patients were treated with 3-dimensional conformal radiation therapy (3D-CRT) APBI. Patients with stage 0, I, or II breast cancer were eligible if a <3-cm tumor was resected with negative surgical margins, and axillary evaluation documented 0-3 positive nodes. The mean age was 58.7 years (range, 31-88 years). Target volume and critical structure definitions, as well as dose delivery guidelines, were consistent across both institutions. Treatment was twice daily for 5 consecutive days with 3.85 Gy per fraction to 38.5 Gy. Clinical follow-up was conducted at regular intervals that included history, physical exam, and mammography. The overall cosmesis was graded using the Harvard scale and toxicity was graded according to the Common Toxicity Criteria (v4.0), including hyperpigmentation, edema, telangiectasia, mastalgia, surgical defect, fibrosis, and fat necrosis. Dose-volume histogram and treatment parameters were collected and analyzed.
At a mean follow-up of 44.3 months (range, 2-94 months), there were 4 cases of grade 3-4 toxicity (7%): 1 patient with mastalgia; 1 patient with mastalgia and fat necrosis; 1 patient with telangiectasia; and 1 patient with fibrosis. There was no statistical correlate between dosimetric parameters and cosmetic outcome. Overall cosmetic outcome was good or excellent in 58 breasts (95%) and "fair to poor" in 3 (5%). There were no local-regional failures; 3 patients failed distantly (5%).
Accelerated partial breast irradiation using 3D-CRT is safe and the risk of serious chronic side effect is low and acceptable.
评估接受辅助性三维适形放疗(3D-CRT)加速部分乳腺照射(APBI)的早期乳腺癌患者的美容效果和毒性反应。
2003年11月至2006年6月,对59例患者的60个乳房进行了三维适形放射治疗(3D-CRT)APBI。0期、I期或II期乳腺癌患者,若肿瘤<3 cm且手术切缘阴性,腋窝评估显示0-3个阳性淋巴结,则符合入选标准。平均年龄为58.7岁(范围31-88岁)。两个机构的靶区体积和危及器官定义以及剂量给予指南均一致。连续5天每天照射两次,每次3.85 Gy,总剂量38.5 Gy。定期进行临床随访,包括病史、体格检查和乳腺X线摄影。使用哈佛量表对总体美容效果进行分级,根据常见毒性标准(第4.0版)对毒性反应进行分级,包括色素沉着、水肿、毛细血管扩张、乳腺疼痛、手术缺损、纤维化和脂肪坏死。收集并分析剂量体积直方图和治疗参数。
平均随访44.3个月(范围2-94个月),有4例3-4级毒性反应(7%):1例乳腺疼痛;1例乳腺疼痛伴脂肪坏死;1例毛细血管扩张;1例纤维化。剂量学参数与美容效果之间无统计学相关性。58个乳房(95%)的总体美容效果为良好或优秀,3个乳房(5%)为“一般至较差”。无局部区域复发;3例患者远处转移(5%)。
使用3D-CRT进行加速部分乳腺照射是安全的,严重慢性副作用的风险低且可接受。