Department of Radiation Oncology, University Hospital Schleswig-Holstein, Arnold-Heller-Str. 3, 24105, Kiel, Germany.
Department of Radiation Oncology, St. Marien-Krankenhaus, Siegen, Germany.
Strahlenther Onkol. 2021 Apr;197(4):269-280. doi: 10.1007/s00066-020-01744-3. Epub 2021 Jan 28.
Moderate hypofractionation is the standard of care for adjuvant whole-breast radiotherapy after breast-conserving surgery for breast cancer. Recently, 10-year results from the FAST and 5‑year results from the FAST-Forward trial evaluating adjuvant whole-breast radiotherapy in 5 fractions over 5 weeks or 1 week have been published. This article summarizes recent data for moderate hypofractionation and results from the FAST and FAST-Forward trial on ultra-hypofractionation. While the FAST trial was not powered for comparison of local recurrence rates, FAST-Forward demonstrated non-inferiority for two ultra-hypofractionated regimens in terms of local control. In both trials, the higher-dose experimental arms resulted in elevated rates of late toxicity. For the lower dose experimental arms of 28.5 Gy over 5 weeks and 26 Gy over 1 week, moderate or marked late effects were similar in the majority of documented items compared to the respective standard arms, but significantly worse in some subdomains. The difference between the standard arm and the 26 Gy of the FAST-Forward trial concerning moderate or marked late effects increased with longer follow-up in disadvantage of the experimental arm for most items. For now, moderate hypofractionation with 40-42.5 Gy over 15-16 fractions remains the standard of care for the majority of patients with breast cancer who undergo whole-breast radiotherapy without regional nodal irradiation after breast-conserving surgery.
中度适形分割放疗是乳腺癌保乳手术后辅助全乳放疗的标准治疗方法。最近,FAST 研究的 10 年结果和 FAST-Forward 研究的 5 年结果相继发表,这两项研究评估了 5 周内 5 次或 1 周内 1 次分割的辅助全乳放疗。本文总结了目前关于中度适形分割放疗的最新数据,以及 FAST 和 FAST-Forward 试验关于超适形分割放疗的结果。虽然 FAST 试验没有对局部复发率进行比较的效能,但 FAST-Forward 试验表明两种超适形分割方案在局部控制方面具有非劣效性。在这两项试验中,高剂量实验组的晚期毒性发生率更高。在 28.5Gy 分 5 周和 26Gy 分 1 周的低剂量实验组中,与标准组相比,大多数记录项目的中度或显著晚期效应相似,但在一些子域中显著更差。与标准组相比,FAST-Forward 试验中 26Gy 实验组的中度或显著晚期效应差异随着随访时间的延长而增大,大多数项目对实验组不利。目前,对于大多数接受保乳手术后全乳放疗且未行区域淋巴结放疗的乳腺癌患者,40-42.5Gy 分 15-16 次仍是标准治疗方法。