Timothy James Pengilley Bray1, Saurabh Singh1, Arash Latifoltojar1, Kannan Rajesparan1, Farzana Rahman1, Alan Bainbridge2, Shonit Punwani1, and Margaret A Hall-Craggs1
1Centre for Medical Imaging, University College London, London, United Kingdom, 2Medical Physics, University College London, London, United Kingdom
Synopsis
Dixon
imaging is becoming more widely used in multiple myeloma (MM) and can provide
both functional and anatomical information. We observed that myeloma lesions
seemed more conspicuous on fat only (FO) images than on conventional in-phase
T1, and therefore hypothesised that lesion detection rates would be higher on
FO images. In this research, we show that reader sensitivity, positive
predictive value and confidence are indeed higher on FO images. This may be
because myeloma lesions cause a proportionately greater change in fat content
than in water content. We suggest that Dixon imaging should be used in
preference to T1 imaging alone when performing WB-MRI. Introduction
Whole body MRI (WBMRI) has
an increasingly important role in the assessment and monitoring of multiple
myeloma (MM) 1,2. Dixon imaging is becoming
more widely used in MM and can provide both functional 3,4 and anatomical
information. We observed that myeloma lesions seemed more conspicuous on fat only
images than on conventional T1-weighted images, suggesting that Dixon imaging
may offer additional information compared to T1-weighted images alone.
In this study, we evaluate
myeloma lesion detection rates on the four Dixon image types: in phase (IP),
out of phase (OP), water only (WO) and fat only (FO) (Figure 1). We
hypothesised that lesion detection rates (sensitivity) would be highest on the fat
only images.
Materials and Methods
Thirty patients (13 male
and 17 female, median age 55, range 36-82) with suspected multiple myeloma underwent
WBMRI imaging on a 3.0T wide-bore system (Ingenia; Phillips Healthcare, Best,
Netherlands) using two anterior surface coils, a head coil and an integrated
posterior coil. The WBMRI protocol included coronal pre- and post-contrast
modified Dixon (mDixon) acquisitions from which fat and water images and
calculated in and out of phase images were reconstructed (TR 3.0ms, TE 1.02-18,
flip angle 15°, slice thickness 5mm,
pixel bandwidth 1992Hz, acquisition matrix 196*238, SENSE factor 2, number of
slices 120) and diffusion and post-contrast imaging, covering vertex
to toe using ten anatomical stations.
Each patient had four image series (i.e. IP, OP, FO and WO). The individual series were randomised and read by two consultant radiologists with
expertise in musculoskeletal and haematological imaging respectively. On each series, each observer was asked to count the number of myeloma lesions present in
the bony pelvis (pubis, ischium, ilium and sacrum) and label these lesions on
the images (up to a maximum of 20). If the disease was diffuse (or there were
over 20 lesions), the patient was assigned a lesion count of 20. Additionally,
the observers were asked to provide a confidence score based on their degree of
certainty that there were myeloma lesions in the pelvis (1-no lesions,
2-indeterminate lesions, 3-likely myeloma lesions, 4-very likely myeloma
lesions). After scoring, each labelled lesion was compared to a reference standard consisting
of diffusion-weighted and post-contrast imaging, which had been evaluated by a further consultant radiologist with expertise in musculoskeletal imaging.
For each image series,
we compared each lesion with the reference standard to determine the number of per-series true positive lesions (TP), false positive lesions (FP) (i.e. those that were
incorrectly identified as lesions); and false negative lesions (FN) (these were
the reference lesions which were not identified). For each Dixon image type, we recorded the mean per-series lesion count,
sensitivity (TP/TP+FN), positive predictive value (TP/TP + FP) and mean
confidence score.
Results
Two observers read 120 image series each for 30 patients (four series per patient) and identified 609 and 789 lesions respectively.
1560 reference lesions were identified.
The mean number of lesions
for each image type was as follows: 8 for FO, 6.5 for WO, 6 for IP and 5.6 for
OP (Figure 2). The sensitivity for each image type was: FO, 54%; IP, 38%; WO,
37% and OP 30%. The positive predictive values were: IP, 79%; FO 79%; WO, 73%;
and OP, 64%. The mean confidence scores were: FO 2.8, WO 2.8, IP
2.6, and OP 2.6.
Discussion
These results suggest that
lesion detection rates are highest on FO images compared to other Dixon image
types. Furthermore, the positive predictive values for FO images are comparable
with IP images and higher than that of OP and WO, suggesting that the increase
in sensitivity reflects a true increase in conspicuity rather than a lower reader
‘threshold’ for lesion identification. Readers also reported the highest
overall confidence scores on the FO images. This may be because there
is a proportionately greater change in bone marrow fat content than in water
content when the bone marrow becomes infiltrated.
Importantly, many centres use solely T1-weighted (i.e. in phase) imaging in their WBMRI protocols for multiple myeloma; these results suggest that Dixon imaging should be used in preference to T1-weighted imaging alone.
In this study, we have not
obtained confidence limits for sensitivity comparisons between modalities
across the entire cohort. A potential solution would be to perform
a meta-analysis (treating each patient in the cohort as an individual study) to
definitively establish differences in sensitivity between modalities.
Conclusion
FO images offer improved
lesion detection rates compared to IP imaging. Dixon imaging provides additional information with minimal increase in scan time and
should be used in preference to T1-weighted imaging alone.
Acknowledgements
No acknowledgement found.References
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