PMID- 25838186 OWN - NLM STAT- MEDLINE DCOM- 20150731 LR - 20220410 IS - 1879-355X (Electronic) IS - 0360-3016 (Print) IS - 0360-3016 (Linking) VI - 92 IP - 2 DP - 2015 Jun 1 TI - High-quality t2-weighted 4-dimensional magnetic resonance imaging for radiation therapy applications. PG - 430-7 LID - S0360-3016(15)00141-8 [pii] LID - 10.1016/j.ijrobp.2015.01.035 [doi] AB - PURPOSE: The purpose of this study was to improve triggering efficiency of the prospective respiratory amplitude-triggered 4-dimensional magnetic resonance imaging (4DMRI) method and to develop a 4DMRI imaging protocol that could offer T2 weighting for better tumor visualization, good spatial coverage and spatial resolution, and respiratory motion sampling within a reasonable amount of time for radiation therapy applications. METHODS AND MATERIALS: The respiratory state splitting (RSS) and multi-shot acquisition (MSA) methods were analytically compared and validated in a simulation study by using the respiratory signals from 10 healthy human subjects. The RSS method was more effective in improving triggering efficiency. It was implemented in prospective respiratory amplitude-triggered 4DMRI. 4DMRI image datasets were acquired from 5 healthy human subjects. Liver motion was estimated using the acquired 4DMRI image datasets. RESULTS: The simulation study showed the RSS method was more effective for improving triggering efficiency than the MSA method. The average reductions in 4DMRI acquisition times were 36% and 10% for the RSS and MSA methods, respectively. The human subject study showed that T2-weighted 4DMRI with 10 respiratory states, 60 slices at a spatial resolution of 1.5 x 1.5 x 3.0 mm(3) could be acquired in 9 to 18 minutes, depending on the individual's breath pattern. Based on the acquired 4DMRI image datasets, the ranges of peak-to-peak liver displacements among 5 human subjects were 9.0 to 12.9 mm, 2.5 to 3.9 mm, and 0.5 to 2.3 mm in superior-inferior, anterior-posterior, and left-right directions, respectively. CONCLUSIONS: We demonstrated that with the RSS method, it was feasible to acquire high-quality T2-weighted 4DMRI within a reasonable amount of time for radiation therapy applications. CI - Copyright (c) 2015 Elsevier Inc. All rights reserved. FAU - Du, Dongsu AU - Du D AD - Department of Radiation Oncology, Washington University School of Medicine, Saint Louis, Missouri. FAU - Caruthers, Shelton D AU - Caruthers SD AD - Philips Healthcare, Cleveland, Ohio. FAU - Glide-Hurst, Carri AU - Glide-Hurst C AD - Department of Radiation Oncology, Henry Ford Health System, Detroit, Michigan. FAU - Low, Daniel A AU - Low DA AD - Department of Radiation Oncology, University of California-Los Angeles, Los Angeles, California. FAU - Li, H Harold AU - Li HH AD - Department of Radiation Oncology, Washington University School of Medicine, Saint Louis, Missouri. FAU - Mutic, Sasa AU - Mutic S AD - Department of Radiation Oncology, Washington University School of Medicine, Saint Louis, Missouri. FAU - Hu, Yanle AU - Hu Y AD - Department of Radiation Oncology, Washington University School of Medicine, Saint Louis, Missouri; Department of Radiation Oncology, Mayo Clinic in Arizona, Phoenix, Arizona. Electronic address: Hu.Yanle@mayo.edu. LA - eng GR - R21 CA167092/CA/NCI NIH HHS/United States GR - 1R21CA167092/CA/NCI NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Validation Study DEP - 20150330 PL - United States TA - Int J Radiat Oncol Biol Phys JT - International journal of radiation oncology, biology, physics JID - 7603616 SB - IM MH - Adult MH - *Algorithms MH - Efficiency MH - Female MH - Healthy Volunteers MH - Humans MH - *Liver MH - Magnetic Resonance Imaging/*methods/standards MH - Male MH - *Movement MH - Radiotherapy/*methods/standards MH - *Respiration MH - Software MH - Time Factors PMC - PMC4431950 MID - NIHMS676838 COIS- Conflict of interest: Dr. Caruthers is an employee of Phillips Healthcare. EDAT- 2015/04/04 06:00 MHDA- 2015/08/01 06:00 PMCR- 2016/06/01 CRDT- 2015/04/04 06:00 PHST- 2014/09/06 00:00 [received] PHST- 2015/01/12 00:00 [revised] PHST- 2015/01/27 00:00 [accepted] PHST- 2015/04/04 06:00 [entrez] PHST- 2015/04/04 06:00 [pubmed] PHST- 2015/08/01 06:00 [medline] PHST- 2016/06/01 00:00 [pmc-release] AID - S0360-3016(15)00141-8 [pii] AID - 10.1016/j.ijrobp.2015.01.035 [doi] PST - ppublish SO - Int J Radiat Oncol Biol Phys. 2015 Jun 1;92(2):430-7. doi: 10.1016/j.ijrobp.2015.01.035. Epub 2015 Mar 30.