Tumor sensitive matching flow: A variational method to detecting and segmenting perihepatic and perisplenic ovarian cancer metastases on contrast-enhanced abdominal CT.


Journal Article

Accurate automated segmentation and detection of ovarian cancer metastases may improve the diagnosis and prognosis of women with ovarian cancer. In this paper, we focus on an important subset of ovarian cancer metastases that spread to the surface of the liver and spleen. Automated ovarian cancer metastasis detection and segmentation are very challenging problems to solve. These metastases have a wide variety of shapes and intensity values similar to that of the liver, spleen and adjacent soft tissues. To address these challenges, this paper presents a variational approach, called tumor sensitive matching flow (TSMF), to detect and segment perihepatic and perisplenic ovarian cancer metastases. TSMF is an image motion field that only highlights metastasis-caused deformation on the surface of liver and spleen while dampening all other image motion between the patient image and the atlas image. It provides several benefits: (1) juxtaposing the roles of image matching and metastasis classification within a variational framework; (2) only requiring a small set of features from a few patient images to train a metastasis-likelihood function for classification; and (3) dynamically creating shape priors for geodesic active contour (GAC) to prevent inaccurate metastasis segmentation. We compared the TSMF to an organ surface partition (OSP) baseline approach. At a false positive rate of 2 per patient, the sensitivities of TSMF and OSP were 87% and 17% (p<0.001), respectively. In a comparison of the segmentations conducted using TSMF-constrained GAC and conventional GAC, the volume overlap rates were 73 ± 9% and 46 ± 26% (p<0.001) and average surface distances were 2.4 ± 1.2 mm and 7.0 ± 6.0 mm (p<0.001), respectively. These encouraging results demonstrate that TSMF could accurately detect and segment ovarian cancer metastases.

Full Text

Cited Authors

  • Liu, J; Wang, S; Linguraru, MG; Yao, J; Summers, RM

Published Date

  • July 2014

Published In

Volume / Issue

  • 18 / 5

Start / End Page

  • 725 - 739

PubMed ID

  • 24835180

Pubmed Central ID

  • 24835180

Electronic International Standard Serial Number (EISSN)

  • 1361-8423

International Standard Serial Number (ISSN)

  • 1361-8415

Digital Object Identifier (DOI)

  • 10.1016/j.media.2014.04.001


  • eng