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原发性和转移性肝脏恶性肿瘤患者的图像引导立体定向体部放疗(SBRT)与肿瘤及肝实质的强化可视化

Image-Guided Stereotactic Body Radiotherapy (SBRT) with Enhanced Visualization of Tumor and Hepatic Parenchyma in Patients with Primary and Metastatic Liver Malignancies.

作者信息

Kirichenko Alexander V, Lee Danny, Wagner Patrick, Oh Seungjong, Lee Hannah, Pavord Daniel, Shamsesfandabadi Parisa, Chen Allen, Machado Lorenzo, Bunker Mark, Sanguino Angela, Shah Chirag, Uemura Tadahiro

机构信息

Division of Radiation Oncology, Allegheny Health Network Cancer Institute, Pittsburgh, PA 15212, USA.

Division of Surgical Oncology, Allegheny Health Network Cancer Institute, Pittsburgh, PA 15212, USA.

出版信息

Cancers (Basel). 2025 Mar 25;17(7):1088. doi: 10.3390/cancers17071088.

DOI:10.3390/cancers17071088
PMID:40227630
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11988117/
Abstract

GOAL

This study evaluates the feasibility and outcome of a personalized MRI-based liver SBRT treatment planning platform with the SPION contrast agent Ferumoxytol (Sandoz Inc.; Princeton, NJ, USA) to maintain a superior real-time visualization of liver tumors and volumes of functional hepatic parenchyma for radiotherapy planning throughout multi-fractionated liver SBRT with online plan adaptations on an Elekta Unity 1.5 T MR-Linac (Elekta; Stockholm, Sweden).

MATERIALS AND METHODS

Patients underwent SPION-enhanced MRI on the Elekta Unity MR-Linac for improved tumor and functional hepatic parenchyma visualization. An automated contouring algorithm was applied for the delineation and subsequent guided avoidance of functional liver parenchyma volumes (FLVs) on the SPION-enhanced MR-Linac. Radiation dose constraints were adapted exclusively to FLV. Local control, toxicity, and survival were assessed with at least 6-month radiographic follow-up. Pre- and post-transplant outcomes were analyzed in the subset of patients with HCC and hepatic cirrhosis who completed SBRT as a bridge to liver transplant. Model of End-Stage Liver Disease (MELD-Na) was used to score hepatic function before and after SBRT.

RESULTS

With a median follow-up of 23 months (range: 3-40 months), 23 HCC patients (26 lesions treated) and 9 patients (14 lesions treated) with hepatic metastases received SBRT (mean dose: 48 Gy, range: 36-54 Gy) in 1-5 fractions. Nearly all patients in this study had pe-existing liver conditions, including hepatic cirrhosis (23), prior TACE (7), prior SBRT (18), or history of hepatic resection (2). Compared to the non-contrast images, SPIONs improved tumor visibility on post-SPION images on the background of negatively enhancing functionally active hepatic parenchyma. Prolonged SPION-contrast retention within hepatic parenchyma enabled per-fraction treatment adaptation throughout the entire multi-fraction treatment course. FLV loss (53%, < 0.0001) was observed in cirrhotic patients, but functional and anatomic liver volumes remained consistent in non-cirrhotic patients. Mean dose to FLV was maintained within the liver threshold tolerance to radiation in all patients after the optimization of Step-and-Shoot Intensity-Modulated Radiotherapy (SS-IMRT) on the SPION-enhanced MRI-Linac. No radiation-induced liver disease was observed within 6 months post-SBRT, and the MELD-Na score in cirrhotic patients was not significantly elevated at 3-month intervals after SBRT completion.

CONCLUSIONS

SPION Ferumoxytol administered intravenously as an alternative MRI contrast agent on the day of SBRT planning produces a long-lasting contrast effect between tumors and functional hepatic parenchyma for precision targeting and guided avoidance during the entire course of liver SBRT, enabling fast and accurate online plan adaptation on the 1.5 T Elekta Unity MR-Linac. This approach demonstrates a safe and effective bridging therapy for patients with hepatic cirrhosis, leading to low toxicity and favorable transplant outcomes.

摘要

目的

本研究评估基于个性化磁共振成像(MRI)的肝脏立体定向体部放疗(SBRT)治疗计划平台的可行性和疗效,该平台使用超顺磁性氧化铁(SPION)造影剂菲立磁(山德士公司;美国新泽西州普林斯顿),以在使用医科达Unity 1.5T MR直线加速器(医科达;瑞典斯德哥尔摩)进行多分割肝脏SBRT且具备在线计划调整功能的整个过程中,保持对肝脏肿瘤和功能性肝实质体积的卓越实时可视化,用于放疗计划。

材料与方法

患者在医科达Unity MR直线加速器上接受SPION增强MRI检查,以改善肿瘤和功能性肝实质的可视化。应用自动轮廓勾画算法在SPION增强的MR直线加速器上勾画并随后引导避开功能性肝实质体积(FLV)。放射剂量限制仅根据FLV进行调整。通过至少6个月的影像学随访评估局部控制、毒性和生存率。对完成SBRT作为肝移植桥梁的肝癌和肝硬化患者亚组分析移植前后的结果。使用终末期肝病模型(MELD-Na)对SBRT前后的肝功能进行评分。

结果

中位随访23个月(范围:3 - 40个月),23例肝癌患者(治疗26个病灶)和9例肝转移患者(治疗14个病灶)接受了1 - 5分割的SBRT(平均剂量:48 Gy,范围:36 - 54 Gy)。本研究中几乎所有患者都有既往肝脏疾病,包括肝硬化(23例)、既往经动脉化疗栓塞术(TACE)(7例)、既往SBRT(18例)或肝切除史(2例)。与非增强图像相比,在功能活跃的肝实质呈负性增强的背景下,SPIONs提高了SPION增强图像上肿瘤的可见性。肝实质内SPION造影剂的长时间保留使得在整个多分割治疗过程中能够进行每次分割的治疗调整。在肝硬化患者中观察到FLV减少(53%,<0.0001),但非肝硬化患者的功能性和解剖性肝脏体积保持一致。在SPION增强的MRI直线加速器上优化步进式调强放疗(SS-IMRT)后,所有患者肝脏内FLV的平均剂量均保持在肝脏对辐射的阈值耐受范围内。SBRT后6个月内未观察到放射性肝病,肝硬化患者在SBRT完成后3个月间隔时MELD-Na评分未显著升高。

结论

在SBRT计划当天静脉注射SPION菲立磁作为替代MRI造影剂,可在肝脏SBRT的整个过程中在肿瘤与功能性肝实质之间产生持久的对比效果,用于精确靶向和引导避开,从而在1.5T医科达Unity MR直线加速器上实现快速准确的在线计划调整。这种方法为肝硬化患者展示了一种安全有效的桥接治疗方法,导致低毒性和良好的移植结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/e9f39eea588a/cancers-17-01088-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/cb005aeb6be8/cancers-17-01088-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/52f15b87d5a2/cancers-17-01088-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/ee488ee2d85a/cancers-17-01088-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/5583755b0343/cancers-17-01088-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/86b473354f75/cancers-17-01088-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/f55e4cb41b62/cancers-17-01088-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/0ca70d0e1a97/cancers-17-01088-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/52149d382d18/cancers-17-01088-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/e9f39eea588a/cancers-17-01088-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/cb005aeb6be8/cancers-17-01088-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/52f15b87d5a2/cancers-17-01088-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/ee488ee2d85a/cancers-17-01088-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/5583755b0343/cancers-17-01088-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/86b473354f75/cancers-17-01088-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/f55e4cb41b62/cancers-17-01088-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/0ca70d0e1a97/cancers-17-01088-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/52149d382d18/cancers-17-01088-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b754/11988117/e9f39eea588a/cancers-17-01088-g009.jpg

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