Schmid Maximilian P, Nesvacil Nicole, Pötter Richard, Kronreif Gernot, Kirisits Christian
Department of Radiation Oncology, Comprehensive Cancer Center, Medical University of Vienna, Austria.
Department of Radiation Oncology, Comprehensive Cancer Center, Medical University of Vienna, Austria.
Radiother Oncol. 2016 Sep;120(3):467-472. doi: 10.1016/j.radonc.2016.01.021. Epub 2016 Feb 23.
To compare the maximum high risk clinical target volume (CTV) dimensions and image quality between magnetic resonance imaging (MRI), transrectal ultrasound (TRUS) and computed tomography (CT) in image guided adaptive brachytherapy (IGABT) of locally advanced cervical cancer.
All patients with locally advanced cervical cancer treated with radiochemotherapy and IGABT between 09/2012-05/2013 were included in this study. T2-weighted MRI (1.5 tesla), TRUS and CT were performed before (MRI, TRUS) and/or after (MRI, TRUS and CT) insertion of the applicator. 3D TRUS image acquisition was done with a customized US stepper device and software. The HR CTV was defined on 3D image sequences acquired with different imaging modalities by one blinded observer, in accordance to the GEC-ESTRO recommendations for MRI-based target volume delineation, as the complete cervical mass including the tumour, any suspicious areas of parametrial involvement and the normal cervical stroma. Maximum HR CTV width and thickness were measured on transversal planes. Image quality was classified using the following scoring system: Grade 0: not depicted, Grade 1: inability to discriminate, margin not recognizable, Grade 2: fair discrimination, margin indistinct, Grade 3: excellent discrimination, margin distinct. Descriptive statistics, mean differences between the groups, with MRI as reference, and a paired t-test were calculated.
Images from 19 patients (FIGO IB: 3, IIB: 9, IIIB: 5, IVB: 2) were available for analysis. The mean difference in maximum HR CTV width of TRUS TRUS MRI CT to MRI was 0.0mm±4.7 (n.s.), -1.1mm±5.6 (n.s.), 0.7mm±6.4 (n.s.) and 13.8mm±6.7 (p<0.001). The mean difference in maximum HR CTV thickness of TRUS TRUS MRI CT to MRI was -3.4mm±5.9 (p=0.037), -3.4mm±4.2 (p<0.001), 2.0mm±6.1 (n.s.) and 13.9mm±6.3 (p<0.001). Mean scores of image quality of the target volume was 2.9 for TRUS, 2.3 for TRUS, 2.9 for MRI, 2.7 for MRI and 2.1 for CT.
For the assessment of the HR CTV in IGABT of cervical cancer, TRUS is within the intraobserver variability of MRI. TRUS is superior to CT as it yields systematically smaller deviations from MRI, with good to excellent image quality. Small differences of TRUS HR CTV thickness are likely related to differences in image slice orientation and compression of the cervix by the TRUS probe before insertion of the brachytherapy applicator.
比较磁共振成像(MRI)、经直肠超声(TRUS)和计算机断层扫描(CT)在局部晚期宫颈癌图像引导下自适应近距离放射治疗(IGABT)中最大高风险临床靶区(CTV)尺寸及图像质量。
本研究纳入2012年9月至2013年5月期间接受放化疗及IGABT治疗的所有局部晚期宫颈癌患者。在施源器插入前(MRI、TRUS)和/或插入后(MRI、TRUS和CT)进行T2加权MRI(1.5特斯拉)、TRUS和CT检查。使用定制的超声步进装置和软件进行3D TRUS图像采集。由一名盲法观察者根据GEC-ESTRO基于MRI的靶区勾画建议,在不同成像方式获取的3D图像序列上定义HR CTV,即完整的宫颈肿物,包括肿瘤、任何可疑的宫旁受累区域及正常宫颈基质。在横断面测量最大HR CTV宽度和厚度。使用以下评分系统对图像质量进行分类:0级:未显示;1级:无法辨别,边缘不可识别;2级:辨别尚可,边缘模糊;3级:辨别出色,边缘清晰。计算描述性统计量、以MRI为参照的组间平均差异及配对t检验。
有19例患者(国际妇产科联盟(FIGO)分期:IB期3例、IIB期9例、IIIB期5例、IVB期2例)的图像可供分析。TRUS与MRI相比,最大HR CTV宽度的平均差异为0.0mm±4.7(无统计学意义),TRUS与MRI相比为-1.1mm±5.6(无统计学意义),CT与MRI相比为0.7mm±6.4(无统计学意义),而TRUS与MRI相比为13.8mm±6.7(p<0.001)。TRUS与MRI相比,最大HR CTV厚度的平均差异为-3.4mm±5.9(p=0.037),TRUS与MRI相比为-3.4mm±4.2(p<0.001),CT与MRI相比为2.0mm±6.1(无统计学意义),而TRUS与MRI相比为13.9mm±6.3(p<0.