Fröhlich Georgina, Mészáros Norbert, Smanykó Viktor, Polgár Csaba, Major Tibor
Centre of Radiotherapy, National Institute of Oncology, Budapest, Hungary.
Faculty of Natural Sciences, Eötvös Loránd University, Budapest, Hungary.
J Contemp Brachytherapy. 2020 Oct;12(5):462-469. doi: 10.5114/jcb.2020.100379. Epub 2020 Oct 30.
To develop an alternative method for summing biologically effective doses of external beam radiotherapy (EBRT) with interstitial high-dose-rate (HDR) brachytherapy (BT) boost in breast cancer. The total doses using EBRT boost were compared with BT boost using our method.
Twenty-four EBRT plus interstitial HDR-BT plans were selected, and additional plans using EBRT boost were created. The prescribed dose was 2.67/40.05 Gy to whole breast and 4.75/14.25 Gy BT or 2.67/10.7 Gy EBRT to planning target volume (PTV) boost. EBRT and BT computed tomography (CT) were registered twice, including fitting the target volumes and using the lung, and the most exposed volume of critical organs in BT were identified on EBRT CT images. The minimal dose of these from EBRT was summed with their BT dose, and these EQD2 doses were compared using BT vs. EBRT boost. This method was compared with uniform dose conception (UDC).
D of PTV boost was significantly higher with BT than with EBRT boost: 67.1 Gy vs. 56.7 Gy, = 0.0001. There was no significant difference in the dose of non-target and contralateral breast using BT and EBRT boost. D to skin, lung, and D to heart were 58.6 Gy vs. 66.7 Gy ( = 0.0025), 32.6 Gy vs. 50.6 Gy ( = 0.0002), and 52.2 Gy vs. 58.1 Gy ( = 0.0009), respectively, while D to ribs was 44.3 Gy vs. 37.7 Gy ( = 0.0062). UDC overestimated D (lung) by 54% ( = 0.0001) and D (ribs) by 28% ( = 0.0003).
Based on our biological dose summation method, the total dose of PTV in the breast is higher using BT boost than with EBRT. BT boost yields lower skin, lung, and heart doses, but higher dose to ribs. UDC overestimates lung and ribs doses.
开发一种用于计算乳腺癌外照射放疗(EBRT)与组织间高剂量率(HDR)近距离放疗(BT)增敏联合生物等效剂量的替代方法。使用我们的方法将EBRT增敏的总剂量与BT增敏的总剂量进行比较。
选取24个EBRT联合组织间HDR-BT计划,并创建使用EBRT增敏的额外计划。全乳的处方剂量为2.67/40.05 Gy,计划靶体积(PTV)增敏的BT剂量为4.75/14.25 Gy或EBRT剂量为2.67/10.7 Gy。EBRT和BT的计算机断层扫描(CT)进行了两次配准,包括拟合靶体积并考虑肺部,在EBRT CT图像上识别出BT中关键器官的最大受照体积。将EBRT中这些器官的最小剂量与它们的BT剂量相加,并使用BT增敏与EBRT增敏比较这些等效均匀剂量(EQD2)。将该方法与均匀剂量概念(UDC)进行比较。
PTV增敏的剂量,BT组显著高于EBRT组:67.1 Gy对56.7 Gy,P = 0.0001。使用BT增敏和EBRT增敏时,非靶区和对侧乳腺的剂量无显著差异。皮肤、肺的剂量以及心脏的剂量分别为58.6 Gy对66.7 Gy(P = 0.0025)、32.6 Gy对50.6 Gy(P = 0.0002)以及52.2 Gy对58.1 Gy(P = 0.0009),而肋骨的剂量为44.3 Gy对37.7 Gy(P = 0.0062)。UDC高估了肺部剂量54%(P = 0.0001)和肋骨剂量28%(P = 0.0003)。
基于我们的生物剂量求和方法,乳腺癌中使用BT增敏时PTV的总剂量高于EBRT。BT增敏使皮肤、肺和心脏的剂量降低,但肋骨剂量更高。UDC高估了肺部和肋骨的剂量。