Katrinus Keijnemans , Tim Schakel , Bastien Lecoeur , Pim T.S. Borman , William A. Hall , Bas W. Raaymakers , Andreas Wetscherek , Eric S. Paulson , Martin F. Fast
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This study combines visual biofeedback (VBF) with 4D-MRI sequences to facilitate in vivo comparisons.</div></div><div><h3>Materials and Methods:</h3><div>Fourteen healthy volunteers and one patient were scanned on a 1.5 T Unity MR-linear accelerator (Elekta AB, Stockholm, Sweden) at two institutions. A radial stack-of-stars (SoS), a simultaneous multi-slice (SMS), and a Cartesian acquisition with spiral ordering (CASPR) 4D-MRI sequence were acquired. These acquisitions were performed without and with VBF based on an interleaved one-dimensional respiratory navigator (1D-RNAV) acquisition. Breathing variability across sequences was quantified using 1D-RNAV-derived breathing waveforms. Reconstructed 4D-MRI data were used to extract the motion amplitude, which was compared intra-volunteer across sequences and to the amplitudes of the breathing waveforms.</div></div><div><h3>Results:</h3><div>Breathing variability across sequences decreased by 37% (amplitude, <em>p</em> <span><math><mo>=</mo></math></span> 0.039) and 64% (period, <em>p</em> <span><math><mo><</mo></math></span> 0.003), and the median intra-volunteer 4D-MRI-derived motion amplitude agreement improved from 3.5 mm to 1.8 mm (<em>p</em> <span><math><mo>=</mo></math></span> 0.064) across sequences due to VBF guidance. Four-dimensional MRI-derived amplitudes were smaller than breathing waveform amplitudes, with median differences of -31% (SoS), -17% (SMS), and -9% (CASPR). The average breathing waveform amplitude was 8% larger than instructed.</div></div><div><h3>Conclusions:</h3><div>This methodology enables in vivo comparisons of 4D-MRI sequences for adaptive radiotherapy, with guidance improving anatomical consistency and ensuring more reliable comparisons.</div></div>","PeriodicalId":36850,"journal":{"name":"Physics and Imaging in Radiation Oncology","volume":"35 ","pages":"Article 100815"},"PeriodicalIF":3.3000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enabling in vivo comparisons of different four-dimensional magnetic resonance imaging sequences for radiotherapy guidance using visual biofeedback\",\"authors\":\"Katrinus Keijnemans , Tim Schakel , Bastien Lecoeur , Pim T.S. Borman , William A. Hall , Bas W. Raaymakers , Andreas Wetscherek , Eric S. Paulson , Martin F. Fast\",\"doi\":\"10.1016/j.phro.2025.100815\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background and Purpose:</h3><div>Managing respiratory motion is essential for effective radiotherapy in the abdominothoracic regions. Respiratory-correlated four-dimensional magnetic resonance imaging (4D-MRI) can provide accurate motion estimation to help define treatment volumes for adaptive radiotherapy. However, validating and comparing 4D-MRI sequences in vivo is challenging due to the presence of breathing variability. This study combines visual biofeedback (VBF) with 4D-MRI sequences to facilitate in vivo comparisons.</div></div><div><h3>Materials and Methods:</h3><div>Fourteen healthy volunteers and one patient were scanned on a 1.5 T Unity MR-linear accelerator (Elekta AB, Stockholm, Sweden) at two institutions. A radial stack-of-stars (SoS), a simultaneous multi-slice (SMS), and a Cartesian acquisition with spiral ordering (CASPR) 4D-MRI sequence were acquired. These acquisitions were performed without and with VBF based on an interleaved one-dimensional respiratory navigator (1D-RNAV) acquisition. Breathing variability across sequences was quantified using 1D-RNAV-derived breathing waveforms. Reconstructed 4D-MRI data were used to extract the motion amplitude, which was compared intra-volunteer across sequences and to the amplitudes of the breathing waveforms.</div></div><div><h3>Results:</h3><div>Breathing variability across sequences decreased by 37% (amplitude, <em>p</em> <span><math><mo>=</mo></math></span> 0.039) and 64% (period, <em>p</em> <span><math><mo><</mo></math></span> 0.003), and the median intra-volunteer 4D-MRI-derived motion amplitude agreement improved from 3.5 mm to 1.8 mm (<em>p</em> <span><math><mo>=</mo></math></span> 0.064) across sequences due to VBF guidance. Four-dimensional MRI-derived amplitudes were smaller than breathing waveform amplitudes, with median differences of -31% (SoS), -17% (SMS), and -9% (CASPR). 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引用次数: 0
摘要
背景与目的:控制呼吸运动是腹胸区有效放疗的必要条件。呼吸相关四维磁共振成像(4D-MRI)可以提供准确的运动估计,以帮助确定适应性放疗的治疗量。然而,由于存在呼吸变异性,在体内验证和比较4D-MRI序列具有挑战性。本研究将视觉生物反馈(VBF)与4D-MRI序列相结合,以促进体内比较。材料和方法:在两个机构的1.5 T Unity磁共振直线加速器(Elekta AB, Stockholm, Sweden)上对14名健康志愿者和1名患者进行扫描。获得了径向星团(SoS)、同时多层(SMS)和螺旋有序笛卡尔采集(CASPR) 4D-MRI序列。这些采集是在无VBF和有VBF的情况下进行的,基于交错一维呼吸导航(1D-RNAV)采集。使用1d - rnav衍生的呼吸波形来量化不同序列的呼吸变异性。重建的4D-MRI数据用于提取运动幅度,并将其与志愿者内部序列和呼吸波形的幅度进行比较。结果:呼吸变异性在不同序列间分别下降了37%(幅度,p = 0.039)和64%(周期,p <;0.003),在VBF引导下,志愿者内部4d - mri得出的运动幅度一致性中位数从3.5 mm提高到1.8 mm (p = 0.064)。四维mri衍生振幅小于呼吸波形振幅,中位数差异为-31% (SoS), -17% (SMS)和-9% (CASPR)。平均呼吸波形幅度比指示大8%。结论:该方法能够在体内比较适应放疗的4D-MRI序列,并在指导下提高解剖一致性,确保更可靠的比较。
Enabling in vivo comparisons of different four-dimensional magnetic resonance imaging sequences for radiotherapy guidance using visual biofeedback
Background and Purpose:
Managing respiratory motion is essential for effective radiotherapy in the abdominothoracic regions. Respiratory-correlated four-dimensional magnetic resonance imaging (4D-MRI) can provide accurate motion estimation to help define treatment volumes for adaptive radiotherapy. However, validating and comparing 4D-MRI sequences in vivo is challenging due to the presence of breathing variability. This study combines visual biofeedback (VBF) with 4D-MRI sequences to facilitate in vivo comparisons.
Materials and Methods:
Fourteen healthy volunteers and one patient were scanned on a 1.5 T Unity MR-linear accelerator (Elekta AB, Stockholm, Sweden) at two institutions. A radial stack-of-stars (SoS), a simultaneous multi-slice (SMS), and a Cartesian acquisition with spiral ordering (CASPR) 4D-MRI sequence were acquired. These acquisitions were performed without and with VBF based on an interleaved one-dimensional respiratory navigator (1D-RNAV) acquisition. Breathing variability across sequences was quantified using 1D-RNAV-derived breathing waveforms. Reconstructed 4D-MRI data were used to extract the motion amplitude, which was compared intra-volunteer across sequences and to the amplitudes of the breathing waveforms.
Results:
Breathing variability across sequences decreased by 37% (amplitude, p 0.039) and 64% (period, p 0.003), and the median intra-volunteer 4D-MRI-derived motion amplitude agreement improved from 3.5 mm to 1.8 mm (p 0.064) across sequences due to VBF guidance. Four-dimensional MRI-derived amplitudes were smaller than breathing waveform amplitudes, with median differences of -31% (SoS), -17% (SMS), and -9% (CASPR). The average breathing waveform amplitude was 8% larger than instructed.
Conclusions:
This methodology enables in vivo comparisons of 4D-MRI sequences for adaptive radiotherapy, with guidance improving anatomical consistency and ensuring more reliable comparisons.