Radiation Oncology Department, Tomotherapy Unit, Ospedale Regionale 'U. Parini', AUSL Valle d'Aosta, Viale Ginevra 3, 11100, Aosta, Italy,
J Cancer Res Clin Oncol. 2013 Nov;139(11):1927-36. doi: 10.1007/s00432-013-1515-0. Epub 2013 Sep 14.
To report the 2-year outcomes of whole breast intensity-modulated radiotherapy (IMRT) after conserving surgery for early breast cancer (EBC) delivered with static angle tomotherapy (TomoDirect) (TD).
A prospective cohort of 120 EBC patients underwent whole breast IMRT with TD between 2010 and 2012. Radiation was delivered to a conventionally fractionated whole breast total dose of 50 Gy with TD, followed by a sequential conventionally fractionated tumor bed boost dose of 10-16 Gy with helical tomotherapy (HT). Clinical endpoints include acute and late toxicity, cosmesis, quality of life and local control.
Median follow-up was 24 months (range 12-36 months); maximum detected acute skin toxicity was G0 22 %; G1 63 %; G2 12 % and G3 3 %. Predictors of acute dermatitis were as follows: volume of the whole breast minus boost volume receiving 105, 110 and 115 % of prescription dose, whole breast and boost volume, breast thickness and soft tissue thickness. Late skin toxicity was mild with no >G2 events. Cosmesis was good/excellent in 91.7 % of patients and fair/poor in 8.3 %. Quality of life was preserved over time, but for fatigue, transiently increased.
Adjuvant whole breast IMRT delivered sequentially with both TD and HT provides consistent clinical results. An observed unintended excessive dose outside the tumor bed might increase acute toxicity and eventually affect long-term clinical endpoints. The incorporation of the boost dose within the whole breast phase employing a simultaneous integrated boost (SIB) approach might mitigate this issue.
报告保乳手术后早期乳腺癌(EBC)采用静态角度调强放疗(TomoDirect)(TD)进行全乳调强放疗(IMRT)的 2 年结果。
2010 年至 2012 年期间,对 120 例 EBC 患者进行了全乳 IMRT 与 TD 的前瞻性队列研究。采用 TD 对常规分割的全乳总剂量 50Gy 进行照射,随后采用螺旋断层放疗(HT)对常规分割的肿瘤床序贯加量 10-16Gy。临床终点包括急性和迟发性毒性、美容效果、生活质量和局部控制。
中位随访时间为 24 个月(12-36 个月);最大急性皮肤毒性为 G0 22%;G1 63%;G2 12%和 G3 3%。急性皮炎的预测因素如下:全乳减去加量体积接受处方剂量 105%、110%和 115%的体积、全乳和加量体积、乳房厚度和软组织厚度。迟发性皮肤毒性轻微,无> G2 事件。91.7%的患者美容效果良好/优秀,8.3%的患者美容效果一般/差。随着时间的推移,生活质量得到了保持,但疲劳感暂时增加。
TD 和 HT 序贯应用于辅助性全乳 IMRT 可提供一致的临床结果。观察到肿瘤床外的意外过量剂量可能会增加急性毒性,并最终影响长期临床终点。采用同步综合增敏(SIB)方法将加量剂量纳入全乳照射阶段可能会减轻这个问题。