[OA046] Visualizing sites of increased cellularity and high permeability in soft tissue sarcomas. (August 2018)
- Record Type:
- Journal Article
- Title:
- [OA046] Visualizing sites of increased cellularity and high permeability in soft tissue sarcomas. (August 2018)
- Main Title:
- [OA046] Visualizing sites of increased cellularity and high permeability in soft tissue sarcomas
- Authors:
- Nikiforaki, Katerina
Kalaitzakis, Georgios
Ioannidis, Georgios
Maris, Thomas G.
Marias, Kostas
Karantanas, Apostolos - Abstract:
- Abstract : Purpose: Radiological evaluation of tumor aggressiveness is very frequently based on diffusion and/or perfusion imaging findings and conclusions are used to guide biopsy. The present work describes a post processing process that highlights areas of increased cellularity (low ADC) and also increased vascular transendothelial permeability (high K trans ), two of the most significant markers of malignancy, at the early stage of imaging. Preliminary results tested on 5 patients with soft tissue sarcomas are presented. Methods: Quantitative ADC maps were generated from MR data by pixelwise mono-exponential fitting of multi-b (8b, 0–1500) DW images with custom-built tools written in Python. Similarly, K trans map was calculated based on the Extended Tofts Model from T1-w GRE data (temporal resolution 7 s, 45 time points). All pixel values assigned as tumor volume (3D ROI) were used as input for the initial whole tumor ADC and K trans histograms. As a next step, only pixels with values lower than the mean of ADC histogram and K trans values greater than the mean K trans were located and visualized in order to examine if a voxel cluster with adequate size is discriminated after thresholding. Patient population (5 male, mean age 60) comprised 3 dedifferentiated liposarcomas and 2 pleomorphic liposarcomas. Results: Whole tumor pixel percentages with ADC value below the mean ADC value of the same ROI (used as histogram threshold) for the five high grade liposarcomas were:Abstract : Purpose: Radiological evaluation of tumor aggressiveness is very frequently based on diffusion and/or perfusion imaging findings and conclusions are used to guide biopsy. The present work describes a post processing process that highlights areas of increased cellularity (low ADC) and also increased vascular transendothelial permeability (high K trans ), two of the most significant markers of malignancy, at the early stage of imaging. Preliminary results tested on 5 patients with soft tissue sarcomas are presented. Methods: Quantitative ADC maps were generated from MR data by pixelwise mono-exponential fitting of multi-b (8b, 0–1500) DW images with custom-built tools written in Python. Similarly, K trans map was calculated based on the Extended Tofts Model from T1-w GRE data (temporal resolution 7 s, 45 time points). All pixel values assigned as tumor volume (3D ROI) were used as input for the initial whole tumor ADC and K trans histograms. As a next step, only pixels with values lower than the mean of ADC histogram and K trans values greater than the mean K trans were located and visualized in order to examine if a voxel cluster with adequate size is discriminated after thresholding. Patient population (5 male, mean age 60) comprised 3 dedifferentiated liposarcomas and 2 pleomorphic liposarcomas. Results: Whole tumor pixel percentages with ADC value below the mean ADC value of the same ROI (used as histogram threshold) for the five high grade liposarcomas were: 58.7, 82.5, 52.1, 65.7, and 78.8%. Ktrans pixel percentages above the mean K trans (threshold) were: 11.8, 23.4, 4.3, 62.9, 39.9% respectively. The percentage of pixels meeting both criteria for low ADC and high K trans were: 4.2, 14.2, 0.6, 20.1, 15.3% respectively. Conclusion: For 4 out of 5 patients visualization of a pixel cluster with adequate size that can be proposed as suitable site for preoperative needle biopsy was possible. Further appropriate ADC/ K trans thresholding can be used to increase disease conspicuity under certain criteria, depending on the special characteristics of each tumor subtype. … (more)
- Is Part Of:
- Physica medica. Volume 52(2018)Supplement 1
- Journal:
- Physica medica
- Issue:
- Volume 52(2018)Supplement 1
- Issue Display:
- Volume 52, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 52
- Issue:
- 2018
- Issue Sort Value:
- 2018-0052-2018-0000
- Page Start:
- 19
- Page End:
- Publication Date:
- 2018-08
- Subjects:
- Medical physics -- Periodicals
Biophysics -- Periodicals
Biophysics -- Periodicals
Imagerie médicale -- Périodiques
Radiothérapie -- Périodiques
Rayons X -- Sécurité -- Mesures -- Périodiques
Physique -- Périodiques
Médecine -- Périodiques
610.153 - Journal URLs:
- http://www.sciencedirect.com/science/journal/11201797 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/11201797 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/11201797 ↗
http://www.elsevier.com/journals ↗
http://www.physicamedica.com ↗ - DOI:
- 10.1016/j.ejmp.2018.06.118 ↗
- Languages:
- English
- ISSNs:
- 1120-1797
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.070000
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- 7292.xml