Sebastian Bickelhaupt1, Jana Tesdorff1, Frederik Bernd Laun2, Wolfgang Lederer3, Heidi Daniel4, Tristan Amseln Kuder2, Susanne Teiner3, Stefan Delorme2, and Heinz-Peter Schlemmer2
1Department of Radiology, German Cancer Research Center, Heidelberg, Germany, 2Department of Medical Physics in Radiology, German Cancer Research Center, Heidelberg, Germany, 3Radiological Practice at the ATOS Clinic Heidelberg, Heidelberg, Germany, 4Radiology Center Mannheim (RZM), Mannheim, Germany
Synopsis
Additive unenhanced breast MRI prior to biopsy might reduce false
positive x-ray mammograms. Therefore we evaluated the adjunctive diagnostic
value of unenhanced breast MRI with image fusion of DWI and T2-weighted images
and compared it to a side-by-side analysis of the sequences. 30 patients were
included undergoing a 1.5 T breast MRI examination prior biopsy. We found that
reading DWI/T2w-fused images alone decreased the accuracy (81.6% ±2.8%)
compared to the side-by-side analysis (91.6% ± 2.3%)
and significantly reduced the reader confidence significantly
(p<0.001). Therefore fused image series should currently be
considered always
in addition to morphologic images since they could miss important morphologic
information.Purpose:
Within
X-ray breast cancer screening programs about 50% of all biopsies reveal a false
positive finding in terms of a benign lesion (1). Diffusion weighted
breast MRI (DWI-MRM) might allow for a more specific characterization of lesions
found on X-ray mammogram prior to biopsy (2). With
DWI, the background can be suppressed and diffusion-altered focal lesions or
areas will stand out only. It further allows performing image fusion by combining
DWI with the information of unenhanced morphological T2w-sequences, which is similar
to PET-imaging (3). Image
fusion thereby could combine the morphologic information (T2w) and the
biophysiological information (DWI) in one postprocessed image sequence.
We evaluated the
diagnostic value of reading fused MR image series combining diffusion weighted imaging
with background suppression (DWIBS) and morphological T2-weighted sequences for
lesion characterization of suspicious BIRADS 4-5 lesion in X-ray mammograms
prior to biopsy.
Methods:
This retrospective
subgroup analysis was performed within an institutional and governmental review
board approved prospective ongoing study. Written informed consent was obtained.
30 patients (mean age 58.9 years, SD ±6.8 years, range 50-69 years) with indication
for biopsy due to a suspicious findings on screening X-ray mammograms (BIRADS
4-5) were included (December 2014 to February 2015). Preliminary results have
been reported.
Breast MRI was
performed prior biopsy using a 1.5T MR scanner (Ingenia, Philips, Best, the
Netherlands; 7-channel breast coil) in prone position. MRI sequences used for
image fusion (as part of a full diagnostic protocol including contrast enhanced
sequences) were T2w- sequences (transverse, TE 120 msec,
TR 3800 msec, Slice thickness 3mm, FOV 340 x 280 mm, Sense x2, TurboFactor 20) and diffusion weighted imaging with background
suppression (DWIBS; b-values b=0 s/mm² and b=1500 s/mm², transverse, TE
85 msec, TR 7300 msec, Slice thickness 3 mm, FOV 400 x 340 mm, STIR with
Inversion Time 180 msec).
Image
fusion was performed using OsiriX (V.6.0, Switzerland). Distortion was corrected
using point-by-point co-registration. Images were analyzed either using the
fused image series or the conventional side-by-side analysis of DWI and
T2-weighted images. Two blinded readers scored both image series using a Likert
scale from “1= no
suspicious lesion detected” to “5= highly suspicious lesion”; “0= no decision
possible, additive information needed”. The Likert-like scales were dichotomized to enable
analysis of diagnostic accuracies. A Likert-like score of 1, 2 or 3 was
considered as “negative”; 0, 4 or 5 was
considered as a “positive”. Diagnostic confidence
was evaluated using a Likert scale from “0= no confidence” to “5 = recognition with
high confidence”.
Accuracy (positive predictive
value [PPV], negative predictive value [NPV], sensitivity and specificity) was
calculated and ANOVA-test was used to compare confidence (SigmaPlot, Version 12.5).
Results:
Biopsy revealed
malignant lesions in 16/30 participants (53%) in histopathology. The overall
mean accuracy achieved by using the fused image series was 81.6% (± 2.8%,R1
0.80%,R2 0.83%) with a sensitivity of 96.8% (± 4.4%,R2 100%,R1 93.7%) and a
specificity of 64.2% (± 10.1%,R1 57.1%,R2 71.4%). In
contrast the overall mean accuracy achieved by using the side-by-side analysis
of DWI and T2-weighted series was 91.6% (± 2.3%,R1 0.90%,R2 0.93%) with a
sensitivity of 97.7% (± 3.2%,R2 100%,R1 93.3%) and a specificity of 85.7% (± 0%,
R1 85.7%, R2 85.7%) (Example Figure 1). Dichotomized overall
interreader agreement for the fused image series was moderate with a kappa of
0.58 (SE 0.18) and good for the side-by-side analysis (kappa 0.63, SE 0.16). Confidence
was significantly (p<0.001) higher in the side-by-side analysis (median 5,
25%-75% CI 4-5) compared to reading the fused series alone (median 4, 25-75% CI
3-4) (Figure 2).
Discussion:
Image fusion of
diffusion weighted (DWI) and morphological T2-weighted images in breast imaging
could combine morphological information and biophysiological properties of
lesions displayed as one image/series (2, 3).
Using fused image series as a stand-alone-tool for further characterization of
previously known X-ray mammography BIRADS 4/5 lesions however reduced the accuracy
and confidence of lesion characterization compared to reading DWI and
T2-weighted images side-by-side. However, image fusion in unenhanced MRI
protocols can represent an important tool linking morphological and
biophysiological information which can add relevant information i.e. for breast
biopsies or in other malignant gynecological entities such as for parametrial invasion in cancer of the cervix uteri (3).
Conclusion:
Abbreviated,
contrast-agent-free breast MRI consisting of T2-weighted and DWI sequences can
help to noninvasively characterize suspicious lesions found on x-ray
mammography. However fused image series used for lesion characterization in
breast MR should not be read alone but always in addition to morphologic
images, since the overly might obscure subtle but diagnostically important
morphological details.
Acknowledgements
This
work was funded by the Dietmar-Hopp-Foundation.References
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Germany. 2014.
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al. Fast and non-invasive characterization of suspicious lesions detected on
X-ray breast cancer screening– capability of diffusion weighted MRI with
maximum intensity projections. Radiology. 2015 ;"DOI: 10.1148/radiol.2015150425".
3. Park JJ, Kim CK, Park SY, et al. Parametrial Invasion in Cervical
Cancer: Fused T2-weighted Imaging and High-b-Value Diffusion-weighted Imaging
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