Abstract

PURPOSE

Staging of lung cancer is typically performed with fluorodeoxyglucose-positron emission tomography-computed tomography (FDG-PET/CT); however, false positive PET scans can occur due to inflammatory disease. The CT scan is used for anatomic registration and attenuation correction. Herein, we evaluated x-ray attenuation (XRA) within nodes on CT and correlated this with the presence of malignancy in an orthotopic lung cancer model in rats.

METHODS

1×106 NCI-H460 cells were injected transthoracically in six National Institutes of Health nude rats and six animals served as controls. After two weeks, animals were sacrificed; lymph nodes were extracted and scanned with a micro-CT to determine their XRA prior to histologic analysis.

RESULTS

Median CT density in malignant lymph nodes (n=20) was significantly higher than benign lymph nodes (n=12; P = 0.018). Short-axis diameter of metastatic lymph nodes was significantly different than benign nodes (3.4 mm vs. 2.4 mm; P = 0.025). Area under the curve for malignancy was higher for density-based lymph node analysis compared with size measurements (0.87 vs. 0.7).

CONCLUSION

XRA of metastatic mediastinal lymph nodes is significantly higher than benign nodes in this lung cancer model. This suggests that information on nodal density may be useful when used in combination with the results of FDG-PET in determining the likelihood of malignant adenopathy

Details

Title
Increased x-ray attenuation in malignant vs. benign mediastinal nodes in an orthotopic model of lung cancer
Author
Flechsig, Paul; Choyke, Peter; Kratochwil, Clemens; Warth, Arne; Antoch, Gerald; Holland-Letz, Tim; Rath, Daniel; Eichwald, Viktoria; Huber, Peter E; Hans-Ulrich Kauczor; Haberkorn, Uwe; Giesel, Frederik L
Pages
35-39
Section
Chest Imaging - Original Article
Publication year
2016
Publication date
Jan 2016
Publisher
Aves Yayincilik Ltd. STI.
ISSN
13053825
e-ISSN
13053612
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2546114657
Copyright
© 2016. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the associated terms available at https://www.dirjournal.org/en/about-dir-1010