Abstract 463P
Background
T factor depends on consolidation diameter in lung adenocarcinoma. Adenocarcinoma with short consolidation diameter could be indicated for sublobar resection. However, measurement of consolidation diameter under lung window in 2D-CT could be problematic, as the outline is not clear. We evaluated the relationship between consolidation lesion under mediastinal window in 3D-CT and pathological invasiveness, and aimed to predict invasiveness using machine learning algorithm.
Methods
Ninety-five patients who underwent surgical resection of lung adenocarcinoma that is less than 20 mm in diameter and has consolidation were analyzed retrospectively, in our Hospital from 2010 to 2016. The total tumor diameter and the volume and diameter of consolidation were analyzed using thin-slice CT and 3D-CT. Preoperative FDG-PET and serum CEA were also measured. Preinvasive lesion and minimally invasive adenocarcinoma were classified as pathologically non-invasive group, and invasive adenocarcinoma was classified as pathologically invasive group. The statistical differences were assessed by the Mann-Whitney U test or chi-square test. We used two machine learning algorithm. Three logistic regression (LR) models were trained based on sex, total tumor diameter, SUVmax, CEA, and (1) consolidation diameter (LR-Cd), (2) consolidation volume (LR-Cv), (3) consolidation diameter and volume (LD-Cd+Cv). Similarly, three random forest (RF) models were trained (RF-Cd, RF-Cv, RF-Cd+Cv). Patients were split into a training set (n = 76) and test set (n = 19). Model performance was measured area under the curve (AUC), and compared using receiver-operating characteristics curve analysis on the test set.
Results
Twenty-six non-invasive adenocarcinomas and 69 invasive adenocarcinomas were evaluated. The consolidation diameter and volume, and SUVmax of invasive group were significantly greater than those of non-invasive group (p < 0.001). On the test set, AUC of LR-Cd, RF-Cd, LR-Cv, RF-Cv, LR-Cd+Cv and RF-Cd+Cv were 0.687, 0.703,0.628, 0.744, 0.628 and 0.744 respectively.
Conclusions
The pathological invasiveness could be predicted by using machine learning algorithm. Especially, higher AUCs were obtained in RF-Cv and RF-Cd+Cv model.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
27P - The prognostic value of neutrophil to lymphocyte ratio (NLR) and 18F-FDG PET SUV in breast cancer patients underwent neoadjuvant chemotherapy
Presenter: Soong June Bae
Session: Poster display session
Resources:
Abstract
28P - Accuracy of core biopsy in predicting pathologic complete response in the breast in patients with complete/near complete clinical and radiological response (Complete Responders in the Breast – CRBr): A feasibility study
Presenter: Nisha Hariharan
Session: Poster display session
Resources:
Abstract
29P - Tumour response to neoadjuvant chemotherapy in breast cancer: Routine pathologic markers improve the predictive power of a cell-loss metric based on release of thymidine kinase 1 into blood
Presenter: Bernhard Tribukait
Session: Poster display session
Resources:
Abstract
30P - Comparison of metabolic changes between neoadjuvant chemotherapy and neoadjuvant endocrine therapy in premenopausal women with ER positive, HER2 negative breast cancer
Presenter: Ho-hyun Ryu
Session: Poster display session
Resources:
Abstract
31P - Circulating miR-155 as a potential therapeutic monitoring marker in breast cancer
Presenter: Sumadi Lukman Anwar
Session: Poster display session
Resources:
Abstract
32P - Profile of breast cancer epidemiology in Sanglah General Hospital, Denpasar, Bali from 2012 to 2019
Presenter: Citra Aryanti
Session: Poster display session
Resources:
Abstract
33P - Contrast enhanced chest CT in patients with breast cancer: Comprehensive imaging analysis and correlation with biological markers
Presenter: Bo Hwa Choi
Session: Poster display session
Resources:
Abstract
34P - Verification of metabolic regulatory mechanisms in androgen receptor-positive triple negative breast cancer
Presenter: Yuka Asano
Session: Poster display session
Resources:
Abstract
35TiP - Ribociclib plus goserelin with hormonal therapy versus physician choice chemotherapy in pre-/perimenopausal patients with HR+, HER2– inoperable locally advanced breast cancer (ABC): RIGHT choice study
Presenter: Yen-Shen Lu
Session: Poster display session
Resources:
Abstract
36TiP - A prospective study to assess response to neoadjuvant hormonal therapy in postmenopausal women with hormone-receptor positive breast cancer at a regional cancer centre in South India
Presenter: Shina Goyal
Session: Poster display session
Resources:
Abstract