Skip to Main Content

An official website of the United States government

Government Funding Lapse

Because of a lapse in government funding, the information on this website may not be up to date, transactions submitted via the website may not be processed, and the agency may not be able to respond to inquiries until appropriations are enacted. The NIH Clinical Center (the research hospital of NIH) is open. For more details about its operating status, please visit  cc.nih.gov. Updates regarding government operating status and resumption of normal operations can be found at OPM.gov.

Principal Investigator
Name
Hugo Aerts
Degrees
PhD
Institution
Harvard-DFCI
Position Title
Director CIBL
Email
About this CDAS Project
Study
NLST (Learn more about this study)
Project ID
NLST-208
Initial CDAS Request Approval
Apr 26, 2016
Title
AI for Lung Nodule Characterization
Summary
Lung cancer is one of the leading causes of cancer deaths worldwide. The long-term survival rate of lung cancer remains low due to the aggressive and heterogeneous nature of lung tumors. Moreover, most of the patients diagnosed with lung cancer, fall in advance stage categories (40% Stage IV, 30% Stage III), which limits the treatment and/or therapy impact. Therefore early stage detection of lung cancer could improve the long-term survival rate. National lung cancer screening trial (NLST) has shown significant (20%) reduction in Lung cancer mortality using low dose computed tomography. However, the resulting high false positive rates and the requirement of highly skilled staff to manually interpret the screen results limit the broad clinical applications of the screening. The goal of this project is to evaluate and compare different AI techniques to quantify the nodule phenotype. We want to apply a large suite of radiomic features that are able to automatically quantify phenotypic traits in a data driven fashion and evaluate its performance. Furthermore, we want to investigate deep learning techniques (Convolutional neural networks (CNNs), to characterize the nodules and normal tissue. And the end we want to compare and combine both techniques. These investigations could enhance the efficiency and efficacy of lung cancer screening and could be a potential step forward towards the clinical implementations.
Aims

1) Evaluate radiomic metrics derived from nodules and other tissues.

2) Evaluate deep learning metrics extracted from nodules and other tissues

3) Compare radiomics and deep learning techniques.

Collaborators

Chintan Parmar
Patrick Grossmann
Roman Zeleznik