Arp Dennis Tideman, Appelt Ane L, Brøndum Rasmus Froberg, Mikalone Rasa, Nielsen Martin Skovmos, Poulsen Laurids Østergaard
Department of Medical Physics, Oncology, Aalborg University Hospital, Aalborg 9000, Denmark.
Department of Clinical Medicine, Aalborg University, Aalborg 9000, Denmark.
Phys Imaging Radiat Oncol. 2024 Jun 14;31:100599. doi: 10.1016/j.phro.2024.100599. eCollection 2024 Jul.
Delivery of high precision radiotherapy lymph node boosts requires detailed information on the interfraction positional variation of individual lymph nodes. In this study we characterized interfraction positional shifts of suspected malignant lymph nodes for rectal cancer patients receiving long course radiotherapy. Furthermore, we investigated parameters which could affect the magnitude of the position variation.
Fourteen patients from a prospective clinical imaging study with a total of 61 suspected malignant lymph nodes in the mesorectum, presacral, and lateral regions, were included. The primary gross tumor volume (GTV) and all suspected malignant lymph nodes were delineated on six magnetic resonance imaging scans per patient. Positional variation was calculated as systematic and random errors, based on shifts of center-of-mass, and estimated relative to either bony structures or the GTV using a hierarchical linear mixed model.
Depending on location and direction, systematic and random variations (relative to bony structures) were within 0.6-2.8 mm and 0.6-2.9 mm, respectively. Systematic and random variations increased when evaluating position relative to GTV (median increase of 0.6 mm and 0.5 mm, respectively). Correlations with scan time-point and relative bladder volume were found in some directions.
Using linear mixed modeling, we estimated systematic and random positional variation for suspected malignant lymph nodes in rectal cancer patients treated with long course radiotherapy. Statistically significant correlations of the magnitude of the lymph node shifts were found related to scan time-point and relative bladder volume.
实施高精度放疗淋巴结增敏需要有关各个淋巴结分次间位置变化的详细信息。在本研究中,我们对接受长程放疗的直肠癌患者可疑恶性淋巴结的分次间位置移动进行了特征描述。此外,我们还研究了可能影响位置变化幅度的参数。
纳入了一项前瞻性临床影像研究中的14例患者,这些患者在直肠系膜、骶前和外侧区域共有61个可疑恶性淋巴结。在每位患者的6次磁共振成像扫描上勾画原发大体肿瘤体积(GTV)和所有可疑恶性淋巴结。基于质心移位,将位置变化计算为系统误差和随机误差,并使用分层线性混合模型相对于骨结构或GTV进行估计。
根据位置和方向,系统误差和随机误差(相对于骨结构)分别在0.6 - 2.8毫米和0.6 - 2.9毫米范围内。相对于GTV评估位置时,系统误差和随机误差增大(分别中位数增加0.6毫米和0.5毫米)。在某些方向上发现了与扫描时间点和相对膀胱体积的相关性。
使用线性混合模型,我们估计了接受长程放疗的直肠癌患者可疑恶性淋巴结的系统和随机位置变化。发现淋巴结移位幅度与扫描时间点和相对膀胱体积存在统计学上的显著相关性。