scholarly journals Mouse lung automated segmentation tool for quantifying lung tumors after micro-computed tomography

PLoS ONE ◽  
2021 ◽  
Vol 16 (6) ◽  
pp. e0252950
Author(s):  
Mary Katherine Montgomery ◽  
John David ◽  
Haikuo Zhang ◽  
Sripad Ram ◽  
Shibing Deng ◽  
...  

Unlike the majority of cancers, survival for lung cancer has not shown much improvement since the early 1970s and survival rates remain low. Genetically engineered mice tumor models are of high translational relevance as we can generate tissue specific mutations which are observed in lung cancer patients. Since these tumors cannot be detected and quantified by traditional methods, we use micro-computed tomography imaging for longitudinal evaluation and to measure response to therapy. Conventionally, we analyze microCT images of lung cancer via a manual segmentation. Manual segmentation is time-consuming and sensitive to intra- and inter-analyst variation. To overcome the limitations of manual segmentation, we set out to develop a fully-automated alternative, the Mouse Lung Automated Segmentation Tool (MLAST). MLAST locates the thoracic region of interest, thresholds and categorizes the lung field into three tissue categories: soft tissue, intermediate, and lung. An increase in the tumor burden was measured by a decrease in lung volume with a simultaneous increase in soft and intermediate tissue quantities. MLAST segmentation was validated against three methods: manual scoring, manual segmentation, and histology. MLAST was applied in an efficacy trial using a Kras/Lkb1 non-small cell lung cancer model and demonstrated adequate precision and sensitivity in quantifying tumor growth inhibition after drug treatment. Implementation of MLAST has considerably accelerated the microCT data analysis, allowing for larger study sizes and mid-study readouts. This study illustrates how automated image analysis tools for large datasets can be used in preclinical imaging to deliver high throughput and quantitative results.

2011 ◽  
Vol 6 (9) ◽  
pp. 1599-1600 ◽  
Author(s):  
Francesco Fraioli ◽  
Simone Vetere ◽  
Marco Anile ◽  
Federico Venuta

Neoplasia ◽  
2009 ◽  
Vol 11 (1) ◽  
pp. 48-56 ◽  
Author(s):  
Rajkumar Savai ◽  
Alexander Claus Langheinrich ◽  
Ralph Theo Schermuly ◽  
Soni Savai Pullamsetti ◽  
Rio Dumitrascu ◽  
...  

2008 ◽  
Vol 6 (9) ◽  
pp. 21
Author(s):  
R. Savai ◽  
R.T. Schermuly ◽  
R. Dumitrascu ◽  
S.S. Pullamsetti ◽  
A.C. Langheinrich ◽  
...  

2018 ◽  
Vol 143 (3) ◽  
pp. 319-325 ◽  
Author(s):  
Fabian M. Troschel ◽  
Ravi V. Gottumukkala ◽  
Daniel DiCorpo ◽  
Julia Mario ◽  
Harald C. Ott ◽  
...  

Context.— Lesion localization during intraoperative frozen section of lung resection specimens can be challenging. Imaging could aid lesion localization while enabling 3-dimensional specimen analysis. Objective.— To assess the feasibility of integrating micro–computed tomography (micro-CT) into the perioperative evaluation of fresh surgical lung resection specimens. Design.— Fresh lung specimens from patients with a presumptive diagnosis of lung cancer were imaged with micro-CT prior to routine histopathologic and molecular analysis. Micro-CT images were assessed to determine image quality, lesion size, and distance from lesion to the nearest surgical margin. Micro-CT measurements were compared to pathologic measurements using Bland-Altman analysis. Results.— A total of 22 specimens from 21 patients were analyzed (mean image acquisition time, 13 ± 6 minutes). Histologic quality of imaged specimens was indistinguishable from a control group of nonimaged lung specimens. Artifacts, most commonly from specimen deflation (n = 8), obscured fine detail on micro-CT images of 10 specimens. Micro-CT could successfully localize the target lesion in the other 12 specimens. Distance to the nearest surgical margin was determined in 10 specimens. Agreement of micro-CT with final pathology was good, with a mean difference of −2.8% (limits of agreement −14.5% to 20.0%) for lesion size and −0.5 mm (limits of agreement −4.4 to 3.4 mm) for distance to nearest surgical margin. Conclusions.— Micro-CT of fresh surgical lung specimens is feasible and has the potential to evaluate the size and location of lesions within resection specimens, as well as distance to the nearest surgical margin, all without compromising specimen integrity.


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