Department of Radiation Oncology, Dr. Léon Richard Oncology Centre, Moncton, New Brunswick, Canada.
Department of Oncology, McMaster University, Hamilton, Ontario, Canada.
Int J Radiat Oncol Biol Phys. 2020 Aug 1;107(5):943-948. doi: 10.1016/j.ijrobp.2020.03.049. Epub 2020 Apr 22.
To assess the acute toxicity and quality of life (QOL) of hypofractionation compared with conventional fractionation for whole breast irradiation (WBI) after breast-conserving surgery.
Women with node-negative breast cancer who had undergone breast-conserving surgery with clear margins were randomly assigned to conventional WBI of 5000 cGy in 25 fractions over 35 days or hypofractionated WBI of 4256 cGy in 16 fractions over 22 days. Acute skin toxicity and QOL were assessed at baseline and 2, 4, 6, and 8 weeks from the start of treatment for a subgroup of patients. QOL was assessed at baseline and 4 weeks posttreatment for all patients. In the acute toxicity substudy, repeated measures modeling was used to investigate treatment by time interactions over the 8-week period for acute toxicity and QOL mean change score. QOL mean change score from baseline to 4 weeks posttreatment was compared for all patients.
In the acute toxicity substudy, 161 patients participated. In the main trial, 1152 patients participated. Acute skin toxicity was initially similar between groups but was less with hypofractionation compared with conventional fractionation toward the end of the 8-week period (P < .001). QOL at 6 weeks from the start of treatment was improved with hypofractionation for the skin side effects, breast side effects, fatigue, attractiveness, and convenience domains (all P < .05). In the main trial, hypofractionation resulted in improved overall QOL and QOL attributed to skin side effects, breast side effects, and attractiveness (all P < .01).
Hypofractionated WBI compared with conventional WBI resulted in less acute toxicity and improved QOL. This further supports the benefits of hypofractionation.
评估保乳手术后全乳照射(WBI)的常规分割与Hypo 分割的急性毒性和生活质量(QOL)。
接受保乳手术且切缘无肿瘤的淋巴结阴性乳腺癌女性患者,被随机分配至接受常规 WBI(5000cGy/25f/35d)或 Hypo 分割 WBI(4256cGy/16f/22d)。在治疗开始后 2、4、6 和 8 周,对部分患者进行急性皮肤毒性和 QOL 评估;所有患者在基线和治疗后 4 周进行 QOL 评估。在急性毒性亚研究中,采用重复测量模型来研究 8 周期间急性毒性和 QOL 平均变化评分的治疗与时间的交互作用。对所有患者进行了治疗后 4 周的 QOL 平均变化评分比较。
在急性毒性亚研究中,有 161 例患者参与;在主要试验中,有 1152 例患者参与。在 8 周的研究过程中,两组患者的急性皮肤毒性起初相似,但 Hypo 组在研究后期的毒性程度低于常规组(P<0.001)。治疗开始后 6 周时,Hypo 组的皮肤副作用、乳房副作用、疲劳、吸引力和便利性的 QOL 得到改善(所有 P<0.05)。在主要试验中,Hypo 组的总体 QOL 和皮肤副作用、乳房副作用和吸引力归因的 QOL 得到改善(所有 P<0.01)。
与常规 WBI 相比,Hypo 分割 WBI 可减轻急性毒性并提高 QOL。这进一步支持了 Hypo 分割的益处。