Diagnostic evaluation of magnetization transfer and diffusion kurtosis imaging for prostate cancer detection in a re-biopsy population
Objective To evaluate diffusion kurtosis imaging (DKI) and magnetisation transfer imaging (MTI) compared to standard MRI for prostate cancer assessment in a re-biopsy population. Methods Thirty-patients were imaged at 3 T including DKI (K app and D app ) with b-values 150/450/800/1150/1500 s/mm 2 an...
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Published in | European radiology Vol. 28; no. 8; pp. 3141 - 3150 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.08.2018
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Objective
To evaluate diffusion kurtosis imaging (DKI) and magnetisation transfer imaging (MTI) compared to standard MRI for prostate cancer assessment in a re-biopsy population.
Methods
Thirty-patients were imaged at 3 T including DKI (K
app
and D
app
) with b-values 150/450/800/1150/1500 s/mm
2
and MTI performed with and without MT saturation. Patients underwent transperineal biopsy based on prospectively defined MRI targets. Receiver-operating characteristic (ROC) analyses assessed the parameters and Wilcoxon-signed ranked test assessed relationships between metrics.
Results
Twenty patients had ≥ 1 core positive for cancer in a total of 26 MRI targets (Gleason 3+3 in 8, 3+4 in 12, ≥ 4+3 in 6): 13 peripheral (PZ) and 13 transition zone (TZ). The apparent diffusion coefficient (ADC) and D
app
were significantly lower and the K
app
and MT ratio (MTR) significantly higher in tumour versus benign tissue (all
p
≤ 0.005); ROC values 0.767-1.000. Normal TZ had: lower ADC and D
app
and higher K
app
and MTR compared to normal PZ. MTR showed a moderate correlation to K
app
(
r
= 0.570) and D
app
(
r
= -0.537) in normal tissue but a poor correlation in tumours. No parameter separated low-grade (Gleason 3+3) from high-grade (≥ 3+4) disease for either PZ (
p
= 0.414-0.825) or TZ (
p
= 0.148-0.825).
Conclusion
ADC, D
app
, K
app
and MTR all distinguished benign tissue from tumour, but none reliably differentiated low- from high-grade disease.
Key Points
•
MTR was significantly higher in PZ and TZ tumours versus normal tissue
•
K
app
was significantly lower and D
app
higher for PZ and TZ tumours
•
There was no incremental value for DKI/MTI over mono-exponential ADC parameters
•
No parameter could consistently differentiate low-grade (Gleason 3+3) from high-grade (≥ 3+4) disease
•
Divergent MTR/DKI values in TZ tumours suggests they offer different functional information |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Undefined-1 ObjectType-Feature-3 content type line 23 |
ISSN: | 0938-7994 1432-1084 |
DOI: | 10.1007/s00330-017-5169-1 |