Linares Isabel, Tovar María Isabel, Zurita Mercedes, Guerrero Rosario, Expósito Manuela, Del Moral Rosario
Department of Radiotherapy and Oncology, Virgen de las Nieves University Hospital, Granada, Spain.
Department of Radiotherapy and Oncology, Virgen de las Nieves University Hospital, Granada, Spain.
Clin Breast Cancer. 2016 Aug;16(4):262-8. doi: 10.1016/j.clbc.2015.09.012. Epub 2015 Sep 25.
We analyzed the toxicity and cosmetic outcomes for patients who had undergone 3-dimensional conformal radiotherapy with a hypofractionated schedule and identified the risk factors associated with such a schedule.
A total of 143 patients were treated for breast cancer (stage 0-III) with a hypofractionated radiation schedule after breast-conserving surgery from 2006 to 2011. Most patients received 42.4 Gy in 16 daily fractions, 2.65 Gy per fraction to the whole breast plus an additional simultaneous integrated or sequential boost to the tumor bed.
The median follow-up period was 36 months. Mild acute skin toxicity was observed in 62%; 7% of the patients developed moderate skin toxicity, but no grade 4 toxicity was observed. The prevalence of fibrosis within the boost area was 5%, but no grade ≥ 2 was observed. The prevalence of fibrosis of any grade was greater in the nonboost (23%) than in the boost area. Of all the patients, 91% had good or excellent cosmetic outcomes. From the multivariate analysis, the incidence of epithelitis correlated with the patient's treated volume (P = .044). The incidence of acute toxicity correlated with the boost type to the tumor bed and the total treatment dose (P = .012 and P = .002, respectively). Also, a poor to fair cosmetic outcome was significantly associated statistically with the surgery type (P = .05), boost type (P = .004), and total dose (P = .001).
Delivering whole-breast irradiation with a hypofractionated schedule of 42.4 Gy plus a simultaneous integrated boost to the tumor bed appears to be a safe and effective technique, with good cosmetic results and lower toxicity.
我们分析了接受三维适形放疗并采用大分割放疗方案的患者的毒性反应和美容效果,并确定了与此种放疗方案相关的风险因素。
2006年至2011年期间,共有143例乳腺癌(0-III期)患者在保乳手术后接受了大分割放疗方案。大多数患者接受42.4 Gy,分16次每日照射,每次2.65 Gy,照射全乳,同时对瘤床进行同步整合加量或序贯加量。
中位随访期为36个月。62%的患者出现轻度急性皮肤毒性;7%的患者出现中度皮肤毒性,但未观察到4级毒性反应。加量区域纤维化的发生率为5%,但未观察到≥2级纤维化。非加量区域任何级别的纤维化发生率(23%)高于加量区域。所有患者中,91%的患者美容效果良好或极佳。多因素分析显示,上皮炎的发生率与患者的受照体积相关(P = 0.044)。急性毒性反应的发生率与瘤床加量类型和总治疗剂量相关(分别为P = 0.012和P = 0.002)。此外,美容效果差至中等与手术类型(P = 0.05)、加量类型(P = 0.004)和总剂量(P = 0.001)在统计学上显著相关。
采用42.4 Gy大分割放疗方案全乳照射并同时对瘤床进行同步整合加量似乎是一种安全有效的技术,美容效果良好且毒性较低。