End-to-End Non–Small-Cell Lung Cancer Prognostication Using Deep Learning Applied to Pretreatment Computed Tomography

2021 ◽  
pp. 1141-1150
Author(s):  
Felipe Soares Torres ◽  
Shazia Akbar ◽  
Srinivas Raman ◽  
Kazuhiro Yasufuku ◽  
Carola Schmidt ◽  
...  

PURPOSE Clinical TNM staging is a key prognostic factor for patients with lung cancer and is used to inform treatment and monitoring. Computed tomography (CT) plays a central role in defining the stage of disease. Deep learning applied to pretreatment CTs may offer additional, individualized prognostic information to facilitate more precise mortality risk prediction and stratification. METHODS We developed a fully automated imaging-based prognostication technique (IPRO) using deep learning to predict 1-year, 2-year, and 5-year mortality from pretreatment CTs of patients with stage I-IV lung cancer. Using six publicly available data sets from The Cancer Imaging Archive, we performed a retrospective five-fold cross-validation using pretreatment CTs of 1,689 patients, of whom 1,110 were diagnosed with non–small-cell lung cancer and had available TNM staging information. We compared the association of IPRO and TNM staging with patients' survival status and assessed an Ensemble risk score that combines IPRO and TNM staging. Finally, we evaluated IPRO's ability to stratify patients within TNM stages using hazard ratios (HRs) and Kaplan-Meier curves. RESULTS IPRO showed similar prognostic power (concordance index [C-index] 1-year: 0.72, 2-year: 0.70, 5-year: 0.68) compared with that of TNM staging (C-index 1-year: 0.71, 2-year: 0.71, 5-year: 0.70) in predicting 1-year, 2-year, and 5-year mortality. The Ensemble risk score yielded superior performance across all time points (C-index 1-year: 0.77, 2-year: 0.77, 5-year: 0.76). IPRO stratified patients within TNM stages, discriminating between highest- and lowest-risk quintiles in stages I (HR: 8.60), II (HR: 5.03), III (HR: 3.18), and IV (HR: 1.91). CONCLUSION Deep learning applied to pretreatment CT combined with TNM staging enhances prognostication and risk stratification in patients with lung cancer.

2021 ◽  
Vol 16 (3) ◽  
pp. S280
Author(s):  
H. Onozawa ◽  
D. Nemoto ◽  
J. Miura ◽  
D. Eriguchi ◽  
H. Adachi ◽  
...  

2021 ◽  
Vol 59 (2) ◽  
pp. 240-246
Author(s):  
Hirohisa Kano ◽  
Toshio Kubo ◽  
Kiichiro Ninomiya ◽  
Eiki Ichihara ◽  
Kadoaki Ohashi ◽  
...  

Radiology ◽  
2021 ◽  
Author(s):  
Yifan Zhong ◽  
Yunlang She ◽  
Jiajun Deng ◽  
Shouyu Chen ◽  
Tingting Wang ◽  
...  

2018 ◽  
Vol Volume 10 ◽  
pp. 5537-5544 ◽  
Author(s):  
Stefan Diem ◽  
Mirjam Fässler ◽  
Omar Hasan Ali ◽  
Marco Siano ◽  
Rebekka Niederer ◽  
...  

Cancers ◽  
2018 ◽  
Vol 10 (10) ◽  
pp. 384 ◽  
Author(s):  
Ashley Hopkins ◽  
Anh-Minh Nguyen ◽  
Christos Karapetis ◽  
Andrew Rowland ◽  
Michael Sorich

Afatinib is an effective therapy for metastatic non-small cell lung cancer (NSCLC) but it is associated with a relatively high incidence of severe diarrhea. The association between pre-treatment candidate predictors (age, sex, race, performance status, renal function, hemoglobin, and measures of body mass) and severe (grade ≥ 3) diarrhea was evaluated using logistic regression with pooled individual participant data from seven clinical studies. A risk score was developed based on the count of major risk factors. Overall, 184 of 1151 participants (16%) experienced severe diarrhea with use of afatinib. Body weight, body mass index, and body surface area all exhibited a prominent non-linear association where risk increased markedly at the lower range (p < 0.005). Low weight (<45 kg), female sex, and older age (≥60 years) were identified as major independent risk factors (p < 0.01). Each risk factor was associated with a two-fold increase in the odds of severe diarrhea, and this was consistent between individuals commenced on 40 mg or 50 mg afatinib. A simple risk score based on the count of these risk factors identifies individuals at lowest and highest risk (C-statistic of 0.65). Risk of severe diarrhea for individuals commenced on 40 mg afatinib ranged from 6% for individuals with no risk factors to 33% for individuals with all three risk factors.


1998 ◽  
Vol 45 (2) ◽  
pp. 322
Author(s):  
Jae Yong Park ◽  
Kwan Young Kim ◽  
Sang Cheol Chae ◽  
Jeong Seok Kim ◽  
Kwon Yeop Kim ◽  
...  

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