Zebin Xiao1, Zuohua Tang2, Jing Zhang3, Guang Yang3, Yang Song3, Linying Guo2, and Zhongshuai Zhang4
1Eye & ENT Hospital of Fudan University, Shanghai, China, 2Radiology, Eye & ENT Hospital of Fudan University, Shanghai, China, 3Shanghai Key Laboratory of Magnetic Resonance, East China Normal University, Shanghai, China, 4MR Scientific Marketing, Siemens Healthcare, Shanghai, China
Synopsis
This is the first study that used histogram metrics
derived from diffusion kurtosis (DKI) and intravoxel incoherent motion (IVIM)
to differentiate sinonasal
mucosal malignant melanomas (SNMMMs) and squamous cell carcinomas (SCCs) which
are sometimes indistinguishable with conventional MRI. Overall, histogram
metrics obtained from K, D, D* and f were found to be significantly higher in SNMMMs than in SCCs.
Furthermore, the combined use of the two independent indicators, the 75th
percentile of K and skewness of D,
can effectively differentiate between SNMMMs and SCCs.
Background and purpose
SNMMMs
are commonly amelanotic (~50%),1 lacking the characteristic melanin signal on conventional MRI2-4. Thus, it is usually
challenging to differentiate SNMMM from most common sinonasal malignant tumor,
SCC. Recently, DKI and IVIM have been shown to be useful
approaches to differentiate between benign and malignant lesions in the
sinonasal region.5, 6
However, no studies applied DKI and IVIM to discriminate SNMMMs from SCCs. Moreover, previous investigations measured DKI
or IVIM parameters from manually placed regions of interest (ROIs) on the
largest section of tumors,5, 6 which could not reflect the characteristic of
the entire tumor. Whole-tumor
histogram analysis could reflect the full spectrum and heterogeneity of
histology within the tumor.7, 8 Thus, the purpose of this study was to evaluate
the diagnostic performance of DKI and IVIM using whole-tumor histogram analysis
for differentiating SNMMMs from SCCs.Methods
DKI and IVIM were performed in 12 patients with SNMMMs
and 26 patients with SCCs on a 3T MR scanner (MAGNETOM
Verio, Siemens Healthcare, Erlangen, Germany). The detailed
parameters were as follows: TR/TE = 5200/83 msec, δ = 27.4 msec, Δ = 39.4 msec, number of averages =
2, acquisition matrix = 120 × 120; field of view (FOV) = 220×220 mm2,
slice thickness = 5 mm, intersection gap = 5 mm, parallel imaging acceleration factor = 2; 14
different b values ranging from 0 to
2500 sec/mm2 were used (b
= 0, 50, 100, 150, 200, 250, 300, 350, 400, 800, 1000, 1500, 2000, and 2500
sec/mm2). The IVIM and DKI
processing were performed using custom-written scripts in MATLAB
(version R2016a; MathWorks, Natick, Mass) to provide ADC, D, D*, f, Dk and K parametric maps on a
pixel-by-pixel basis.9 The whole-tumor histogram
metrics were calculated on these parametric maps using PyRadiomics (version 1.3.0; http://github.com/Radiomics/pyradiomics) based on Python (version 3.5.4; http://www.python.org).10 The Student’s
t-tests, ROC curve and multivariate stepwise logistic regression analyses were used
for statistical analysis.Results
Significantly higher mean, median, 75th and 90th
percentiles of K, skewness of D, mean, median, 90th percentile and kurtosis of D*, 75th and 90th percentiles of f were found in SNMMMs than in SCCs (all P < .05). Higher 75th percentile of K (β
coefficient = 0.007; OR = 1.007, 95% CI = 1.001-1.012; P = 0.026) and skewness of D (β coefficient = 0.209; OR = 1.232,
95% CI = 1.001-1.518; P = 0.049) were independent
indicators for the differentiation of SNMMMs for SCCs. One example of
the calculated DWI parameters, histogram and haematoxylin-eosin
staining of a patient is
shown in Figure 1. The combination of 75th percentile of K and skewness of D can
improve the diagnostic performance with a sensitivity and specificity of 75.0% and
80.8%, respectively, for differentiating these two malignant tumors. The
histogram analysis tool was not given in method secitonConclusion
Whole-tumour histogram analysis of
DKI and IVIM are valuable for differentiating
SNMMMs from SCCs. The 75th percentile of K and skewness of D were independent predictors for
distinguishing between them.Keywords
Neoplasms; Magnetic resonance imaging;
Diffusion magnetic resonance imaging; Melanoma; Squamous cell carcinomaAcknowledgements
This work was
supported by the Grant of Science and Technology Commission of Shanghai
Municipality (Grant number: 17411962100)
and Key Project of the National Natural Science Foundation of China (Grant
number: 61731009).References
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