Ott Oliver J, Stillkrieg Wilhelm, Lambrecht Ulrike, Schweizer Claudia, Lamrani Allison, Sauer Tim-Oliver, Strnad Vratislav, Bert Christoph, Hack Carolin C, Beckmann Matthias W, Fietkau Rainer
Department of Radiation Oncology, Universitätsklinikum Erlangen, 91054 Erlangen, Germany.
Comprehensive Cancer Center Erlangen-EMN, 91054 Erlangen, Germany.
Cancers (Basel). 2023 Jun 9;15(12):3128. doi: 10.3390/cancers15123128.
In order to evaluate organ-at-risk (OAR) doses in external-beam-accelerated partial-breast irradiation (APBI) compared to standard whole-breast irradiation (WBI) after breast-conserving surgery. Between 2011 and 2021, 170 patients with early breast cancer received APBI within a prospective institutional single-arm trial. The prescribed dose to the planning treatment volume was 38 Gy in 10 fractions on 10 consecutive working days. OAR doses for the contralateral breast, the ipsilateral, contralateral, and whole lung, the whole heart, left ventricle (LV), and the left anterior descending coronary artery (LAD), and for the spinal cord and the skin were assessed and compared to a control group with real-world data from 116 patients who underwent WBI. The trial was registered at the German Clinical Trials Registry, DRKS-ID: DRKS00004417. Compared to WBI, APBI led to reduced OAR doses for the contralateral breast (0.4 ± 0.6 vs. 0.8 ± 0.9 Gy, = 0.000), the ipsilateral (4.3 ± 1.4 vs. 9.2 ± 2.5 Gy, = 0.000) and whole mean lung dose (2.5 ± 0.8 vs. 4.9 ± 1.5 Gy, = 0.000), the mean heart dose (1.6 ± 1.6 vs. 1.7 ± 1.4 Gy, = 0.007), the LV V23 (0.1 ± 0.4 vs. 1.4 ± 2.6%, < 0.001), the mean LAD dose (2.5 ± 3.4 vs. 4.8 ± 5.5 Gy, < 0.001), the maximum spinal cord dose (1.5 ± 1.1 vs. 4.5 ± 5.7 Gy, = 0.016), and the maximum skin dose (39.6 ± 1.8 vs. 49.1 ± 5.8 Gy, = 0.000). APBI should be recommended to suitable patients to minimize the risk of secondary tumor induction and the incidence of consecutive major cardiac events.
为了评估保乳手术后,与标准全乳照射(WBI)相比,外照射加速部分乳腺照射(APBI)中危及器官(OAR)的剂量。在2011年至2021年期间,170例早期乳腺癌患者在一项前瞻性机构单臂试验中接受了APBI。计划治疗体积的处方剂量为38 Gy,分10次在连续10个工作日给予。评估了对侧乳腺、同侧、对侧和全肺、全心、左心室(LV)和左前降支冠状动脉(LAD)以及脊髓和皮肤的OAR剂量,并与来自116例行WBI患者的真实世界数据对照组进行比较。该试验已在德国临床试验注册中心注册,注册号:DRKS00004417。与WBI相比,APBI导致对侧乳腺的OAR剂量降低(0.4±0.6 vs. 0.8±0.9 Gy,P = 0.000)、同侧(4.3±1.4 vs. 9.2±2.5 Gy,P = 0.000)和全肺平均剂量降低(2.5±0.8 vs. 4.9±1.5 Gy,P = 0.000)、平均心脏剂量降低(1.6±1.6 vs. 1.7±1.4 Gy,P = 0.007)、LV V23降低(0.1±0.4 vs. 1.4±2.6%,P < 0.001)、平均LAD剂量降低(2.5±3.4 vs. 4.8±5.5 Gy,P < 0.001)、最大脊髓剂量降低(1.5±1.1 vs. 4.5±5.7 Gy,P = 0.016)以及最大皮肤剂量降低(39.6±1.8 vs. 49.1±5.8 Gy,P = 0.000)。应向合适的患者推荐APBI,以尽量降低继发肿瘤诱导风险和连续重大心脏事件的发生率。