Belinda Lokaj1, Karen Kinkel2, Jean-Noel Hyacinthe3, Jérôme Schmid3, and Céline Gaignot3
1Master of Science in Health Sciences, HES-SO /UNIL, Lausanne, Switzerland, Lausanne, Switzerland, 2Institut de radiologie, Clinique des Grangettes, Chêne-Bougeries, Geneva, Switzerland, Geneva, Switzerland, 3Geneva School of Health Sciences, HES-SO // University of Applied Sciences and Arts of Western Switzerland, Geneva, Switzerland
Synopsis
Breast MRI is promoted as a tool for breast cancer
screening because of its high sensitivity. Possibility of differentiating
between benign and malign lesions has been studied using lesion enhancement
parameters on DCE, thus helping to reduce examination time. This study was designed to verify
sensitivity and specificity for lesion characterization. Time to Enhancement and Maximum Slope of the enhancement
curve obtained from an ultrafast sequence were evaluated. Preliminary results
tend to confirm that performing breast lesions screening using ultrafast-DCE is a valuable alternative to the standard MRI Breast protocol, possibly opening diagnostic perspectives to a wider
population of women.
Purpose
Breast MRI is promoted
as a tool for breast cancer screening because it is a very sensitive technique [1].
At present, a complete breast MRI examination lasts about 20 minutes according
to clinical protocols, but the possibility of shortening the
examination time (3 minutes) [2], by focusing on important sequences
such as the DCE sequences is increasingly investigated [3], thus
helping to reduce examination time and accessibility of the MRI for women. Lesion
differentiation between benign and malignant can be performed with ultrafast
dynamic contrast enhanced sequences using kinetic parameters within the first
post contrast minute. This study was designed to verify sensitivity and
specificity for lesion characterization in a clinical high-risk setting
including 24 patients after informed consent. We evaluated specifically Time to
Enhancement and Maximum Slope of the enhancement curve obtained from a
4D-THRIVE MRI sequence and compared results with histopathology and/or
follow-up.Methods
24
breast MRI examinations with visible lesions and performed with a Philips 3T
Ingenia MRI scanner were retrospectively collected. The early enhancement
kinetics parameters acquired with 4D-THRIVE sequence were analyzed using a Philips
Intellispace© console. Maximum slope and Time to enhancement performances
in differentiating benign from malignant lesions were evaluated [4,5].
The MS was calculated using Intellispace© automatic parameters
calculation (MS1) and manually calculating the steepest part of the MRI signal
time evolution (ΔSI/ΔT) (MS2). The agreement between these two methods was
assessed.
Cutoff
values for classification of the lesions in 3 curve types [4]
(<5.5%/sec = Type I; >5.5%/sec to <9%/sec = Type II; >9%/sec =Type
III) were defined, given by MS values and lesion morphology, on a training data
set different from the test dataset described and evaluated here. TTE was calculated as the
difference between the time of visible enhancement of the lesion and the
time of visible enhancement in the aorta. Both MS and TTE diagnosis were
confronted to the histopathology and/or with the follow-up. To assess intra and inter observer
variability, three ROI (Region of Interest) per lesion were performed by two
expert MR technologists and four novice MR technologists.
ROC
analysis was performed to compare MS and TTE.
This pilot study was approved by the Ethics Committee Geneva
(CCER). Project-ID: 2019-0716.Results
A total of 26 lesions were identified:
15 were benign (including 9 lymph nodes),
8 were malignant and 3 were uncertain lesions, as there was no
histopathological result. Lymph nodes
and patients who received chemotherapy treatment were excluded. Our first
results show that MS performs better than TTE, with regards to sensitivity and
specificity. (table 1)
Following ROC analysis (Figure 1), areas under curve (AUC) of 0.93 and
0.26 were respectively computed for MS and TTE.
Relatively good agreement between the two MS methods
was found (figure 2), but we observed that non-continuous enhancement curves (e.g.,
caused by potential respiratory movements) worsened the agreement. This
explains one of the measurements with very low agreement.
Preliminary results for the
intra-observer evaluation suggest good reproducibility for observer A, and good
agreement between observers. However, some results
show bad inter observer agreement especially in lesions with
complex morphology, suggesting a possible learning curve for novice
radiographers that was not evaluated in this study.
The
main limitation of our study is the small size of the collected dataset and the
frequent presence of lymph nodes in our data.
Conclusion
MS calculation appears to be more robust and performs better than TTE estimation in
differentiating benign from malignant lesions. The two methods
of MS calculation can be used because of the good agreement. The first results of intra observer assessment suggest a good
reproducibility. We are currently including more patients as more data are
required for a quantitative analysis. Our Preliminary results tend
to confirm that performing breast lesions screening using ultrafast dynamic MRI
is a valuable alternative to the standard – more time consuming – MRI Breast
protocol, possibly opening diagnostic perspectives to a wider population of
women.Acknowledgements
No acknowledgement found.References
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