Meixner Eva, Harrabi Semi, Seidensaal Katharina, Koczur Beata, Tessonnier Thomas, Lentz-Hommertgen Adriane, Hoeltgen Line, Hoegen-Saßmannshausen Philipp, Weykamp Fabian, Liermann Jakob, Hörner-Rieber Juliane, Debus Jürgen
Department of Radiation Oncology, Heidelberg University Hospital, Im Neuenheimer Feld 400, 69120 Heidelberg, Germany.
Heidelberg Institute of Radiation Oncology (HIRO), 69120 Heidelberg, Germany.
J Clin Med. 2025 May 13;14(10):3416. doi: 10.3390/jcm14103416.
(1) : The management of ipsilateral breast cancer recurrence depends on the extent of the tumor, and staging results, and mastectomy is currently the standard of care for previously irradiated patients. Studies are increasingly investigating suitable candidates for the repeated use of breast-conserving approaches as an alternative to mastectomy. But this includes the crucial necessity for curative reirradiation (Re-RT). The therapeutic challenge in reirradiation involves finding a balance between tumor control and the risk of severe toxicity from cumulative radiation doses in previously irradiated organs. Re-RT options include the use of brachytherapy, intraoperative radiotherapy, or external beam RT with photons or electrons. The application of particle therapy using proton beam therapy represents an innovative radiotherapeutic technique for breast cancer patients that might offer advantageous physical properties, a superior dose reduction to adjacent organs-at-risk, and effective target volume coverage with lower integral doses to the patient's whole body. In addition, this technique could potentially offer higher radiobiological effects and tumor responses. (2) : The BREAST trial (NCT06954623) will be conducted as a prospective, single-arm, phase II study in 20 patients with histologically proven invasive breast cancer recurrences after repeat breast-conserving surgery and with an indication for local reirradiation. The patients will receive partial-breast re-RT with proton beam therapy in 15 once-daily fractions up to a total dose of 40.05 Gy(RBE), delivered with active raster scanning. The required time interval will be 1 year after previous RT to the ipsilateral breast. (3) : The following results will be reported: The primary endpoint is defined as the cumulative overall occurrence of (sub)acute skin toxicity of grade ≥ 3 within 6 months after the start of re-RT. Secondary outcome includes an analysis of the local, regional, and distant control, progression-free and overall survival, quality of life, and cosmesis. The explorative and translational objectives of this study include planning comparisons to other RT techniques and irradiation types, dosimetric evaluations, analyses of radiological imaging features, and translational assessments of cardiac toxicity biomarkers and tumor markers. (4) : Overall, the aim of this study is to evaluate the potential of proton beam therapy for partial breast reirradiation and to establish the underlying data for a randomized trial.
(1):同侧乳腺癌复发的管理取决于肿瘤范围和分期结果,目前对于先前接受过放疗的患者,乳房切除术是标准的治疗方法。越来越多的研究正在调查适合重复使用保乳方法以替代乳房切除术的患者。但这包括进行根治性再放疗(Re-RT)的关键必要性。再放疗中的治疗挑战在于在肿瘤控制与先前接受过放疗的器官因累积辐射剂量导致的严重毒性风险之间找到平衡。再放疗选择包括使用近距离放疗、术中放疗或光子或电子外照射放疗。使用质子束疗法的粒子治疗应用代表了一种针对乳腺癌患者的创新放射治疗技术,它可能具有有利的物理特性,能更好地减少对相邻危险器官的剂量,以较低的全身积分剂量有效覆盖靶体积。此外,该技术可能会提供更高的放射生物学效应和肿瘤反应。(2):BREAST试验(NCT06954623)将作为一项前瞻性、单臂、II期研究,针对20例经组织学证实为浸润性乳腺癌复发且接受过重复保乳手术并有局部再放疗指征的患者进行。患者将接受质子束疗法的部分乳房再放疗,分15次每日一次照射,总剂量达40.05 Gy(相对生物效应),采用主动光栅扫描技术。所需时间间隔为先前对同侧乳房放疗后1年。(3):将报告以下结果:主要终点定义为再放疗开始后6个月内累积发生的≥3级(亚)急性皮肤毒性。次要结果包括对局部、区域和远处控制、无进展生存期和总生存期、生活质量以及美容效果的分析。本研究的探索性和转化性目标包括与其他放疗技术和照射类型进行计划比较、剂量学评估、放射影像学特征分析以及心脏毒性生物标志物和肿瘤标志物的转化评估。(4):总体而言,本研究的目的是评估质子束疗法用于部分乳房再放疗的潜力,并为一项随机试验建立基础数据。