Isaac Daimiel Naranjo1, Roberto Lo Gullo2, Carolina Sacarelli2, Almir Bitencourt2, Peter Gibbs2, Elisabeth Morris2, Caleb Sooknanan2, Jeff Reiner2, Maxine S Jochelson2, Sunitha Thakur2, and Katja Pinker-Domenig2
1Radiology, Memorial Sloan Kettering Cancer Center, NEW YORK, NY, United States, 2Memorial Sloan Kettering Cancer Center, New york, NY, United States
Synopsis
Radiomics coupled with machine learning is based on the extraction of
signatures from medical images that are invisible to the human eye to create
models which would improve breast cancer diagnosis. Radiomics features
extracted from dynamic contrast-enhanced
MRI and diffusion-weighted imaging can be combined in multiparametric MRI. We
hypothesize that radiomics features extracted from multiparametric
MRI would allow for an improved model affording a more accurate breast cancer
diagnosis. We developed a multiparametric model that achieved the best accuracy for breast cancer
diagnosis compared to models based on dynamic
contrast-enhanced MRI or diffusion-weighted imaging.
INTRODUCTION
Dynamic contrast-enhanced MRI (DCE-MRI) is an
image modality with very high sensitivity but low specificity for breast cancer
diagnosis (1). The reason is the overlap in the image characteristics
of benign and malignant enhancing lesions which entails a high
number of false positive diagnoses and unnecessary biopsies. Multiparametric
MRI with diffusion-weighted imaging (DWI) has demonstrated to increase the
specificity for breast cancer diagnosis compared to DCE-MRI alone (2). Currently, radiomics coupled with machine learning (ML)
has mainly focused on extracting features from DCE-MR images with promising results (3). However,
a multiparametric approach could further improve breast cancer diagnosis. With only a few
published studies investigating the performance of radiomics in multiparametric MRI (4) (5) (6), the aim of our work was to evaluate the
diagnostic value of radiomics analysis coupled with ML on multiparametric MRI
for the evaluation of suspicious enhancing breast tumors.METHOD AND MATERIALS
In this IRB- approved
retrospective study 93 women with 104 biopsy-proven suspicious breast lesions (58
benign, 46 malignant) were included. Three-dimensional tumor segmentation was
conducted on DCE-MR images from first post-contrast T1-weighted and ADC maps
derived from DWI by two dedicated breast radiologists with five years of
experience in breast imaging. Radiomics features derived from DCE and DW
images were calculated using the publicly
available computational environment for radiological research software based
on first-order statistics, gray level co-occurrence matrix (GLCM), run length
matrix (RLM), size zone matrix (SZM), neighborhood gray level dependence
matrix, and neighborhood gray tone difference matrix. Univariate and multivariate analysis were
performed to identify significant radiomic features to be included in a ML
model to discriminate between malignant and benign breast lesions. Least
absolute shrinkage and selection operator (LASSO) regression was performed to
prevent overfitting and a
medium Gaussian support vector machine model with five-fold cross validation
was employed to develop the predictive models. A flowchart of the radiomics
analysis is shown in Figure 1. Measures of sensitivity, specificity, negative predictive value
(NPV), positive predictive value (PPV) and accuracy were estimated for DCE-MRI,
DWI and multiparametric MRI models. Classification performance was evaluated using
the receiver operating characteristic curve.RESULTS AND DISCUSSION
102 radiomics parameters
were calculated. Subsequently, univariate modelling
rendered 31 and 41 significant radiomic parameters for ADC and DCE-MRI respectively.
After LASSO regression and multivariate modelling, 6 parameters from DCE-MR images
(entropy, total energy, zln, Joint Variance, inverse variance and coarseness)
and 6 parameters from the DW images (kurtosis, min, entropy, gln Normalized sze
and Irhgle) were used into a medium Gaussian support vector machine model with
five-fold cross validation to develop a final robust ML model.
We achieved sensitivities
of 79.6%, 76.3% and 83.4% and specificities of 69.7%, 78.2% and 81.5% for ADC,
DCE-MRI and multiparametric MRI models respectively. PPV and NPV were 68.4%, 74.3%, 78.8 % and 80.6
%, 80.1%, 85.6% for ADC, DCE-MRI and multiparametric MRI models respectively. The
diagnostic accuracy was 74.2 %, 77.4 % and 82.4% for ADC, DCE-MRI and
multiparametric MRI models respectively. The area under the curve (AUC) was
0.80, 0.84 and 0.86 for ADC, DCE-MRI and multiparametric MRI models respectively.
Radiomics features extracted from
multiparametric MRI allowed the development of a model which maximized diagnostic
accuracy and AUC. These results are in accordance with other group who
developed a multiparametric scheme that achieved an AUC of 0.87 outperforming
DCE (4).
Other groups have incorporated
pharmacokinetic analysis to the
multiparametric model (5) and DWI kurtosis (6) achieving even better
results with AUCs over 0.9. The multiparametric
model achieved a better specificity and PPV compared to the other two models
which indicates that multiparametric models not only have the potential to aid
in breast cancer diagnosis, but also in clinical decision
making to prevent unnecessary biopsies.CONCLUSIONS
We developed a radiomic model derived from multiparametric MRI that yielded
the best diagnostic results for breast cancer diagnosis maximizing diagnostic performance and achieving the best accuracy, highest
specificity and PPV compared to radiomic models
based solely on DCE and DWI extracted features. Radiomics coupled with ML combining features
extracted from multiparametric MRI may help improve breast cancer diagnosis and
prevent unnecessary breast biopsies.Acknowledgements
This work was financially supported by the NIH/NCI Cancer Center Support Grant (P30 CA008748), the Breast Cancer Research Foundation, and the Spanish Foundation Alfonso Martin Escudero. References
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