Performance of a fast and high‐resolution multi‐echo spin‐echo sequence for prostate T2 mapping across multiple systems
Purpose To evaluate the performance of a multi‐echo spin‐echo sequence with k‐t undersampling scheme (k‐t T2) in prostate cancer. Methods Phantom experiments were performed at five systems to estimate the bias, short‐term repeatability, and reproducibility across all systems expressed with the withi...
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Published in | Magnetic resonance in medicine Vol. 79; no. 3; pp. 1586 - 1594 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc
01.03.2018
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ISSN | 0740-3194 1522-2594 1522-2594 |
DOI | 10.1002/mrm.26816 |
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Abstract | Purpose
To evaluate the performance of a multi‐echo spin‐echo sequence with k‐t undersampling scheme (k‐t T2) in prostate cancer.
Methods
Phantom experiments were performed at five systems to estimate the bias, short‐term repeatability, and reproducibility across all systems expressed with the within‐subject coefficient of variation (wCV). Monthly measurements were performed on two systems for long‐term repeatability estimation. To evaluate clinical repeatability, two T2 maps (voxel size 0.8 × 0.8 × 3 mm3; 5 min) were acquired at separate visits on one system for 13 prostate cancer patients. Repeatability was assessed per patient in relation to spatial resolution. T2 values were compared for tumor, peripheral zone, and transition zone.
Results
Phantom measurements showed a small bias (median = −0.9 ms) and good short‐term repeatability (median wCV = 0.5%). Long‐term repeatability was 0.9 and 1.1% and reproducibility between systems was 1.7%. The median bias observed in patients was −1.1 ms. At voxel level, the median wCV was 15%, dropping to 4% for structures of 0.5 cm3. The median tumor T2 values (79 ms) were significantly lower (P < 0.001) than in the peripheral zone (149 ms), but overlapped with the transition zone (91 ms).
Conclusions
Reproducible T2 mapping of the prostate is feasible with good spatial resolution in a clinically reasonable scan time, allowing reliable measurement of T2 in structures as small as 0.5 cm3. Magn Reson Med 79:1586–1594, 2018. © 2017 International Society for Magnetic Resonance in Medicine. |
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AbstractList | To evaluate the performance of a multi-echo spin-echo sequence with k-t undersampling scheme (k-t T2 ) in prostate cancer.PURPOSETo evaluate the performance of a multi-echo spin-echo sequence with k-t undersampling scheme (k-t T2 ) in prostate cancer.Phantom experiments were performed at five systems to estimate the bias, short-term repeatability, and reproducibility across all systems expressed with the within-subject coefficient of variation (wCV). Monthly measurements were performed on two systems for long-term repeatability estimation. To evaluate clinical repeatability, two T2 maps (voxel size 0.8 × 0.8 × 3 mm3 ; 5 min) were acquired at separate visits on one system for 13 prostate cancer patients. Repeatability was assessed per patient in relation to spatial resolution. T2 values were compared for tumor, peripheral zone, and transition zone.METHODSPhantom experiments were performed at five systems to estimate the bias, short-term repeatability, and reproducibility across all systems expressed with the within-subject coefficient of variation (wCV). Monthly measurements were performed on two systems for long-term repeatability estimation. To evaluate clinical repeatability, two T2 maps (voxel size 0.8 × 0.8 × 3 mm3 ; 5 min) were acquired at separate visits on one system for 13 prostate cancer patients. Repeatability was assessed per patient in relation to spatial resolution. T2 values were compared for tumor, peripheral zone, and transition zone.Phantom measurements showed a small bias (median = -0.9 ms) and good short-term repeatability (median wCV = 0.5%). Long-term repeatability was 0.9 and 1.1% and reproducibility between systems was 1.7%. The median bias observed in patients was -1.1 ms. At voxel level, the median wCV was 15%, dropping to 4% for structures of 0.5 cm3 . The median tumor T2 values (79 ms) were significantly lower (P < 0.001) than in the peripheral zone (149 ms), but overlapped with the transition zone (91 ms).RESULTSPhantom measurements showed a small bias (median = -0.9 ms) and good short-term repeatability (median wCV = 0.5%). Long-term repeatability was 0.9 and 1.1% and reproducibility between systems was 1.7%. The median bias observed in patients was -1.1 ms. At voxel level, the median wCV was 15%, dropping to 4% for structures of 0.5 cm3 . The median tumor T2 values (79 ms) were significantly lower (P < 0.001) than in the peripheral zone (149 ms), but overlapped with the transition zone (91 ms).Reproducible T2 mapping of the prostate is feasible with good spatial resolution in a clinically reasonable scan time, allowing reliable measurement of T2 in structures as small as 0.5 cm3 . Magn Reson Med 79:1586-1594, 2018. © 2017 International Society for Magnetic Resonance in Medicine.CONCLUSIONSReproducible T2 mapping of the prostate is feasible with good spatial resolution in a clinically reasonable scan time, allowing reliable measurement of T2 in structures as small as 0.5 cm3 . Magn Reson Med 79:1586-1594, 2018. © 2017 International Society for Magnetic Resonance in Medicine. Purpose To evaluate the performance of a multi‐echo spin‐echo sequence with k‐t undersampling scheme (k‐t T2) in prostate cancer. Methods Phantom experiments were performed at five systems to estimate the bias, short‐term repeatability, and reproducibility across all systems expressed with the within‐subject coefficient of variation (wCV). Monthly measurements were performed on two systems for long‐term repeatability estimation. To evaluate clinical repeatability, two T2 maps (voxel size 0.8 × 0.8 × 3 mm3; 5 min) were acquired at separate visits on one system for 13 prostate cancer patients. Repeatability was assessed per patient in relation to spatial resolution. T2 values were compared for tumor, peripheral zone, and transition zone. Results Phantom measurements showed a small bias (median = −0.9 ms) and good short‐term repeatability (median wCV = 0.5%). Long‐term repeatability was 0.9 and 1.1% and reproducibility between systems was 1.7%. The median bias observed in patients was −1.1 ms. At voxel level, the median wCV was 15%, dropping to 4% for structures of 0.5 cm3. The median tumor T2 values (79 ms) were significantly lower (P < 0.001) than in the peripheral zone (149 ms), but overlapped with the transition zone (91 ms). Conclusions Reproducible T2 mapping of the prostate is feasible with good spatial resolution in a clinically reasonable scan time, allowing reliable measurement of T2 in structures as small as 0.5 cm3. Magn Reson Med 79:1586–1594, 2018. © 2017 International Society for Magnetic Resonance in Medicine. PurposeTo evaluate the performance of a multi‐echo spin‐echo sequence with k‐t undersampling scheme (k‐t T2) in prostate cancer.MethodsPhantom experiments were performed at five systems to estimate the bias, short‐term repeatability, and reproducibility across all systems expressed with the within‐subject coefficient of variation (wCV). Monthly measurements were performed on two systems for long‐term repeatability estimation. To evaluate clinical repeatability, two T2 maps (voxel size 0.8 × 0.8 × 3 mm3; 5 min) were acquired at separate visits on one system for 13 prostate cancer patients. Repeatability was assessed per patient in relation to spatial resolution. T2 values were compared for tumor, peripheral zone, and transition zone.ResultsPhantom measurements showed a small bias (median = −0.9 ms) and good short‐term repeatability (median wCV = 0.5%). Long‐term repeatability was 0.9 and 1.1% and reproducibility between systems was 1.7%. The median bias observed in patients was −1.1 ms. At voxel level, the median wCV was 15%, dropping to 4% for structures of 0.5 cm3. The median tumor T2 values (79 ms) were significantly lower (P < 0.001) than in the peripheral zone (149 ms), but overlapped with the transition zone (91 ms).ConclusionsReproducible T2 mapping of the prostate is feasible with good spatial resolution in a clinically reasonable scan time, allowing reliable measurement of T2 in structures as small as 0.5 cm3. Magn Reson Med 79:1586–1594, 2018. © 2017 International Society for Magnetic Resonance in Medicine. |
Author | Agarwal, Harsh K. Poel, Henk G. Heide, Uulke A. Houdt, Petra J. Heijmink, Stijn W.T.P.J. Peeters, Johannes M. Haack, Søren Ghobadi, Ghazaleh Choyke, Peter L. Buuren, Laurens D. Pos, Floris J. |
AuthorAffiliation | 4 Department of Radiology, the Netherlands Cancer Institute, Amsterdam, the Netherlands 2 Philips Research NA, Cambridge, MA, USA 1 Department of Radiation Oncology, the Netherlands Cancer Institute, Amsterdam, The Netherlands 6 Department of Urology, the Netherlands Cancer Institute, Amsterdam, the Netherlands 5 Department of Clinical Engineering, Aarhus University Hospital, Aarhus, Denmark 7 Philips Healthcare, Best, the Netherlands 3 National Cancer Institute, National Institutes of Health, Bethesda, USA |
AuthorAffiliation_xml | – name: 4 Department of Radiology, the Netherlands Cancer Institute, Amsterdam, the Netherlands – name: 7 Philips Healthcare, Best, the Netherlands – name: 2 Philips Research NA, Cambridge, MA, USA – name: 3 National Cancer Institute, National Institutes of Health, Bethesda, USA – name: 6 Department of Urology, the Netherlands Cancer Institute, Amsterdam, the Netherlands – name: 1 Department of Radiation Oncology, the Netherlands Cancer Institute, Amsterdam, The Netherlands – name: 5 Department of Clinical Engineering, Aarhus University Hospital, Aarhus, Denmark |
Author_xml | – sequence: 1 givenname: Petra J. surname: Houdt fullname: Houdt, Petra J. organization: the Netherlands Cancer Institute – sequence: 2 givenname: Harsh K. surname: Agarwal fullname: Agarwal, Harsh K. organization: National Institutes of Health – sequence: 3 givenname: Laurens D. surname: Buuren fullname: Buuren, Laurens D. organization: the Netherlands Cancer Institute – sequence: 4 givenname: Stijn W.T.P.J. surname: Heijmink fullname: Heijmink, Stijn W.T.P.J. organization: the Netherlands Cancer Institute – sequence: 5 givenname: Søren surname: Haack fullname: Haack, Søren organization: Aarhus University Hospital – sequence: 6 givenname: Henk G. surname: Poel fullname: Poel, Henk G. organization: the Netherlands Cancer Institute – sequence: 7 givenname: Ghazaleh surname: Ghobadi fullname: Ghobadi, Ghazaleh organization: the Netherlands Cancer Institute – sequence: 8 givenname: Floris J. surname: Pos fullname: Pos, Floris J. organization: the Netherlands Cancer Institute – sequence: 9 givenname: Johannes M. surname: Peeters fullname: Peeters, Johannes M. organization: Philips Healthcare – sequence: 10 givenname: Peter L. surname: Choyke fullname: Choyke, Peter L. organization: National Institutes of Health – sequence: 11 givenname: Uulke A. surname: Heide fullname: Heide, Uulke A. email: u.vd.heide@nki.nl organization: the Netherlands Cancer Institute |
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To evaluate the performance of a multi‐echo spin‐echo sequence with k‐t undersampling scheme (k‐t T2) in prostate cancer.
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Phantom experiments... PurposeTo evaluate the performance of a multi‐echo spin‐echo sequence with k‐t undersampling scheme (k‐t T2) in prostate cancer.MethodsPhantom experiments were... To evaluate the performance of a multi-echo spin-echo sequence with k-t undersampling scheme (k-t T2 ) in prostate cancer.PURPOSETo evaluate the performance of... |
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SubjectTerms | Bias Coefficient of variation k‐space undersampling Magnetic resonance Mapping multicenter Patients Performance evaluation Prostate cancer prostate cancer imaging quantitative repeatability Reproducibility Spatial discrimination Spatial resolution Systems analysis T2 mapping |
Title | Performance of a fast and high‐resolution multi‐echo spin‐echo sequence for prostate T2 mapping across multiple systems |
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