TY - JOUR
T1 - Automatic segmentation of subcutaneous mouse tumors by multiparametric MR analysis based on endogenous contrast
AU - Hectors, S.J.C.G.
AU - Jacobs, I.
AU - Strijkers, G.J.
AU - Nicolaij, K.
PY - 2015/8/27
Y1 - 2015/8/27
N2 - Object: Contrast-enhanced T1-weighted imaging is usually included in MRI procedures for automatic tumor segmentation. Use of an MR contrast agent may not be appropriate for some applications, however. We assessed the feasability of automatic tumor segmentation by multiparametric cluster analysis that uses intrinsic MRI contrast only. Materials and methods: Multiparametric MRI consisting of quantitative T1, T2, and apparent diffusion coefficient (ADC) mapping was performed in mice bearing subcutaneous tumors (n = 21). k-means and fuzzy c-means clustering with all possible combinations of MRI parameters, i.e. feature vectors, and 2–7 clusters were performed on the multiparametric data. Clusters associated with tumor tissue were selected on the basis of the relative signal intensity of tumor tissue in T2-weighted images. The optimum segmentation method was determined by quantitative comparison of automatic segmentation with manual segmentation performed by three observers. In addition, the automatically segmented tumor volumes from seven separate tumor data sets were quantitatively compared with histology-derived tumor volumes. Results: The highest similarity index between manual and automatic segmentation (SImanual,automatic = 0.82 ± 0.06) was observed for k-means clustering with feature vector {T2, ADC} and four clusters. A strong linear correlation between automatically and manually segmented tumor volumes (R2 = 0.99) was observed for this segmentation method. Automatically segmented tumor volumes also correlated strongly with histology-derived tumor volumes (R2 = 0.96). Conclusion: Automatic segmentation of mouse subcutaneous tumors can be achieved on the basis of endogenous MR contrast only.
AB - Object: Contrast-enhanced T1-weighted imaging is usually included in MRI procedures for automatic tumor segmentation. Use of an MR contrast agent may not be appropriate for some applications, however. We assessed the feasability of automatic tumor segmentation by multiparametric cluster analysis that uses intrinsic MRI contrast only. Materials and methods: Multiparametric MRI consisting of quantitative T1, T2, and apparent diffusion coefficient (ADC) mapping was performed in mice bearing subcutaneous tumors (n = 21). k-means and fuzzy c-means clustering with all possible combinations of MRI parameters, i.e. feature vectors, and 2–7 clusters were performed on the multiparametric data. Clusters associated with tumor tissue were selected on the basis of the relative signal intensity of tumor tissue in T2-weighted images. The optimum segmentation method was determined by quantitative comparison of automatic segmentation with manual segmentation performed by three observers. In addition, the automatically segmented tumor volumes from seven separate tumor data sets were quantitatively compared with histology-derived tumor volumes. Results: The highest similarity index between manual and automatic segmentation (SImanual,automatic = 0.82 ± 0.06) was observed for k-means clustering with feature vector {T2, ADC} and four clusters. A strong linear correlation between automatically and manually segmented tumor volumes (R2 = 0.99) was observed for this segmentation method. Automatically segmented tumor volumes also correlated strongly with histology-derived tumor volumes (R2 = 0.96). Conclusion: Automatic segmentation of mouse subcutaneous tumors can be achieved on the basis of endogenous MR contrast only.
KW - Cluster analysis
KW - Endogenous contrast
KW - Multiparametric MRI
KW - Tumor segmentation
UR - http://www.scopus.com/inward/record.url?scp=84938823992&partnerID=8YFLogxK
U2 - 10.1007/s10334-014-0472-1
DO - 10.1007/s10334-014-0472-1
M3 - Article
C2 - 25427885
AN - SCOPUS:84938823992
SN - 0968-5243
VL - 28
SP - 363
EP - 375
JO - Magnetic Resonance Materials in Physics, Biology and Medicine
JF - Magnetic Resonance Materials in Physics, Biology and Medicine
IS - 4
ER -