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Table 3 Studies investigating the use of MRI texture analysis in diagnosis, treatment response assessment, and as a prognostic tool

From: Assessment of tumor heterogeneity: an emerging imaging tool for clinical practice?

Diagnosis and characterization

Method

Study findings

Author, year

Diagnosis

Breast

Simulated microcalcification

Texture analysis

Successful automatic detection of localized blurring was achieved (sensitivity = 89 %–94 %; specificity = 99.7 %―100 %; PPV = 74 %–100 %; NPV = 99.9 %–99.9 %)

James et al., 2001 [45]

Breast cancer

Texture analysis

A combination of textural analysis (second-order statistics, e.g., contrast, sum entropy, entropy), lesion size, time to maximum enhancement, and patient age allowed for a diagnostic accuracy of 0.92 ± 0.05

Gibbs et al., 2003 [46]

Breast lesion

Texture analysis

The classification performance of volumetric texture features (second-order statistics) is significantly better than 2D analysis

Chen et al., 2007 [47]

Breast cancer

Texture analysis

The 4D texture analysis (using second-order statistics) achieved a performance comparable to human observers

Woods et al.,2007 [48]

Invasive lobular and ductal breast cancer

Texture analysis

Investigated the use of first-order statistics, second-order stastistics obtained from GLCM, RLM, autoregressive model, and wavelet transform. All parameters distinguished healthy from cancerous tissue although GLCM performed better. 80 %–100 % of accuracy in differentiating ductal from lobular cancers, particularly complexity and entropy

Holli et al., 2010 [22]

Brain

Glioneuronal tumor

Texture analysis

The combination of DCE-MRI and MRI textural analysis (second-order statistics—GLCM and RLM) provide optimal differentiation between glioneuronal tumors and gliomas in vivo

Eliat et al., 2012 [19]

Brain tumors—metastases, meningiomas, gliomas (grade II and III), glioblastomas

Texture analysis

Metastases were successfully distinguished from gliomas (accuracy = 85 %; sensitivity = 87 %; specificity = 79 %) as well as high-grade from low-grade neoplasms (accuracy = 88 %; sensitivity = 85 %; specificity = 96 %) using Gabor transform texture analysis

Zacharaki et al., 2009 [23]

Prostate

Prostate cancer

Fractal analysis

The combination of fractal and multifractal features was more accurate than classical texture features in detecting cancer and was more robust against signal intensity variations

Lopes et al., 2011 [21]

Prostate cancer

Fractal analysis

Both fractal analyses offered promising quantitative indices for prostate cancer identification, with histogram fractal dimension offering a more robust diagnosis than texture fractal analysis (correlation coefficient of c = 0.9905 vs. c = 0.9458, respectively)

Lv et al., 2009 [49]

Liver

Liver cysts and hemangiomas

Texture analysis

Texture analysis (first-order, second-order statistics and wavelet transform) was successfully used to classify focal liver lesions on zero-fill interpolated 3.0-T MR images

Mayerhoefer et al., 2010 [20]

Response assessment

Breast

Texture analysis

Second-order statistics extracted from parametric maps that reflect lesion washout properties discriminate malignant from benign tumors better than textural features extracted from either first post-contrast frame lesion area or from parametric map reflecting lesion initial uptake. Angular second moment and entropy were most discriminative

Karahaliou et al., 2010 [26]

Lymphoma

Texture analysis

Texture analysis [first-order, second-order statistics (GLCM and RLM), autoregressive model and wavelet transform] was able to classify NHL lesions undergoing chemotherapy based on changes following treatment

Harrison et al.,2009 [27]

Liver metastases

Fractal analysis

Tumor heterogeneity as assessed by fractal dimension predicted tumor shrinkage in response to bevacizumab and cytotoxic chemotherapy in colorectal liver metastases

O’Connor et al., 2011 [28]