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减少 DCE-MRI 引导 SBRT 中钆基对比剂的剂量:对早期乳腺癌患者术前靶区勾画的观察者内和观察者间变异性的影响。

Reducing the dose of gadolinium-based contrast agents for DCE-MRI guided SBRT: The effects on inter and intra observer variability for preoperative target volume delineation in early stage breast cancer patients.

机构信息

Medical Biophysics, Western University, London, Canada.

Lawson Health Research Institute, London, Canada.

出版信息

Radiother Oncol. 2019 Feb;131:60-65. doi: 10.1016/j.radonc.2018.11.020. Epub 2018 Dec 29.

Abstract

BACKGROUND AND PURPOSE

This study aimed to determine the effects of reducing the dose of contrast agent (CA) in a DCE-MRI scan on inter- and intra-observer variability in the context of MRI-guided target volume delineation for stereotactic body radiation therapy of early stage breast cancer patients. This is in hopes of reducing risks to patients due to findings of residual CA in brain and bone.

MATERIALS AND METHODS

Twenty-three patients receiving neoadjuvant radiation therapy were enrolled. Five observers delineated the gross target volume (GTV) using DCE-MRI for guidance. 14/23 patients received the full clinical dose of CA and 9/23 received half. Clinical target volumes (CTV) were created through a 0.5 cm uniform expansion. Several metrics were used to quantify the inter and intra-observer reliability including differences in delineation volume and the reliability coefficient.

RESULTS

There were no significant differences in the volume, though half contrast patients had a lower median for both the GTV and CTV (difference of 0.26 cm and 1.27 cm, respectively). All indicated a high degree of agreement between and within observers for both dose groups. However, the full dose group had a greater inter-observer variability, most likely due to the full CA causing more pronounced enhancement in the periphery.

CONCLUSIONS

Reducing the dose of contrast agent did not significantly alter inter- or intra-observer variability. These results have prompted our centre to reduce the dose of gadolinium in all patients enrolled in the SIGNAL trial.

摘要

背景与目的

本研究旨在确定在 MRI 引导的立体定向体部放射治疗早期乳腺癌患者靶区勾画中,减少对比剂(CA)剂量对磁共振弥散加权成像(DCE-MRI)扫描中观察者间和观察者内变异性的影响。这是为了减少由于脑和骨中残留 CA 而给患者带来的风险。

材料与方法

纳入 23 例接受新辅助放疗的患者。5 名观察者使用 DCE-MRI 勾画大体肿瘤靶区(GTV)。14/23 例患者接受全临床剂量 CA,9/23 例患者接受半剂量 CA。临床靶区(CTV)通过 0.5cm 的均匀外扩获得。使用多种指标来量化观察者间和观察者内的可靠性,包括勾画体积差异和可靠性系数。

结果

尽管半剂量 CA 的 GTV 和 CTV 的中位数均较低(分别为 0.26cm 和 1.27cm),但两组间的体积差异无统计学意义。两组观察者间和观察者内均有高度一致性。然而,全剂量组的观察者间变异性更大,这可能是由于全剂量 CA 在外周引起了更明显的增强。

结论

减少对比剂剂量不会显著改变观察者间或观察者内的变异性。这些结果促使我们中心在 SIGNAL 试验中所有入组患者减少钆剂剂量。

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