A Novel Polymer-Encapsulated Multi-Imaging Modality Fiducial Marker with Positive Signal Contrast for Image-Guided Radiation Therapy

被引:0
|
作者
Wang, Li [1 ]
Sanders, Jeremiah [2 ]
Ward, John F. [3 ]
Lee, Stephen R. [4 ]
Poenisch, Falk [5 ]
Swanson, David Michael [6 ]
Sahoo, Narayan [5 ]
Zhu, Xiaorong Ronald [5 ]
Ma, Jingfei [2 ]
Kudchadker, Rajat J. [5 ]
Choi, Seungtaek L. [7 ]
Nguyen, Quynh-Nhu [7 ]
Mayo, Lauren L. [7 ]
Shah, Shalin J. [7 ]
Frank, Steven J. [7 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Radiat Oncol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Imaging Phys, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Urol, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Intervent Radiol, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Radiat Phys, Houston, TX 77030 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[7] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
radiation therapy; prostate cancer; magnetic resonance imaging; fiducial marker; NOVA; MONTE-CARLO SIMULATIONS; PROSTATE BRACHYTHERAPY; PROTON THERAPY; DOSE PERTURBATIONS; DOSIMETRIC IMPACT; GOLD MARKERS; BONY ANATOMY; LOCALIZATION; CANCER; RADIOTHERAPY;
D O I
10.3390/cancers16030625
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Current fiducial markers (FMs) in external-beam radiotherapy (EBRT) for prostate cancer (PCa) cannot be positively visualized on magnetic resonance imaging (MRI) and create dose perturbation and significant imaging artifacts on computed tomography (CT) and MRI. We report our initial experience with clinical imaging of a novel multimodality FM, NOVA. Methods: We tested Gold Anchor [G-FM], BiomarC [carbon, C-FM], and NOVA FMs in phantoms imaged with kilovoltage (kV) X-rays, transrectal ultrasound (TRUS), CT, and MRI. Artifacts of the FMs on CT were quantified by the relative streak artifacts level (rSAL) metric. Proton dose perturbations (PDPs) were measured with Gafchromic EBT3 film, with FMs oriented either perpendicular to or parallel with the beam axis. We also tested the performance of NOVA-FMs in a patient. Results: NOVA-FMs were positively visualized on all 4 imaging modalities tested. The rSAL on CT was 0.750 +/- 0.335 for 2-mm reconstructed slices. In F-tests, PDP was associated with marker type and depth of measurement (p < 10(-6)); at 5-mm depth, PDP was significantly greater for the G-FM (12.9%, p = 10(-6)) and C-FM (6.0%, p = 0.011) than NOVA (4.5%). EBRT planning with MRI/CT image co-registration and daily alignments using NOVA-FMs in a patient was feasible and reproducible. Conclusions: NOVA-FMs were positively visible and produced less PDP than G-FMs or C-FMs. NOVA-FMs facilitated MRI/CT fusion and identification of regions of interest.
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页数:15
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