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 inMagnetic resonance in medicine Vol. 79; no. 3; pp. 1586 - 1594
Main Authors Houdt, Petra J., Agarwal, Harsh K., Buuren, Laurens D., Heijmink, Stijn W.T.P.J., Haack, Søren, Poel, Henk G., Ghobadi, Ghazaleh, Pos, Floris J., Peeters, Johannes M., Choyke, Peter L., Heide, Uulke A.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc 01.03.2018
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ISSN0740-3194
1522-2594
1522-2594
DOI10.1002/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.
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
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Snippet 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...
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
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fmrm.26816
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