CANCER-RADIOMICS | Deep Learning for Automated Quantification of Radiographic Tumor Phenotypes

Summary
Artificial Intelligence (AI), deep-learning in particular, is propelling the field of radiology forward at a rapid pace. In oncology, AI can characterize the radiomic phenotype of the entire tumor and provide a non-invasive window into the internal growth patterns of a cancer lesion. This is especially important for patients treated with immunotherapy as, despite the remarkable success of these novel therapies, the clinical benefit remains limited to a subset. As immunotherapy is expensive and could bring unnecessary toxicity there is a direct need to identify beneficial patients, but this remains difficult in clinical practice today. Radiomic biomarkers could address this, as, unlike biopsies that only represent a sample within the tumor, radiomics can depict a full picture of each cancer lesion with a single non-invasive examination. Previous work found significant connections between radiomic data, molecular pathways, and clinical outcomes. However, a direct link between radiomics and immunotherapy response has not yet been established. This project will address this problem by analyzing unique multicentre clinical data, including non-invasive imaging, clinical outcomes, and extensive biologic characterization of patients with lung or melanoma cancer. Specifically, I will develop deep-learning radiomic biomarkers to predict immunotherapy response using baseline (WP1) and follow-up imaging (WP2). I will also investigate if radiomics can characterize underlying biological factors, and, in turn, can be used to improve response predictions (WP3). Successful completion of this proposal will demonstrate the potential of radiomics to help physicians in selecting patients who will likely benefit from immunotherapy, while sparing this expensive and potentially toxic treatment for patients who don't. This work has implications for the use of imaging-based biomarkers in the clinic, as they can be applied noninvasively, repeatedly, and at low additional cost.
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More information & hyperlinks
Web resources: https://cordis.europa.eu/project/id/866504
Start date: 01-08-2020
End date: 31-07-2025
Total budget - Public funding: 2 000 000,00 Euro - 2 000 000,00 Euro
Cordis data

Original description

Artificial Intelligence (AI), deep-learning in particular, is propelling the field of radiology forward at a rapid pace. In oncology, AI can characterize the radiomic phenotype of the entire tumor and provide a non-invasive window into the internal growth patterns of a cancer lesion. This is especially important for patients treated with immunotherapy as, despite the remarkable success of these novel therapies, the clinical benefit remains limited to a subset. As immunotherapy is expensive and could bring unnecessary toxicity there is a direct need to identify beneficial patients, but this remains difficult in clinical practice today. Radiomic biomarkers could address this, as, unlike biopsies that only represent a sample within the tumor, radiomics can depict a full picture of each cancer lesion with a single non-invasive examination. Previous work found significant connections between radiomic data, molecular pathways, and clinical outcomes. However, a direct link between radiomics and immunotherapy response has not yet been established. This project will address this problem by analyzing unique multicentre clinical data, including non-invasive imaging, clinical outcomes, and extensive biologic characterization of patients with lung or melanoma cancer. Specifically, I will develop deep-learning radiomic biomarkers to predict immunotherapy response using baseline (WP1) and follow-up imaging (WP2). I will also investigate if radiomics can characterize underlying biological factors, and, in turn, can be used to improve response predictions (WP3). Successful completion of this proposal will demonstrate the potential of radiomics to help physicians in selecting patients who will likely benefit from immunotherapy, while sparing this expensive and potentially toxic treatment for patients who don't. This work has implications for the use of imaging-based biomarkers in the clinic, as they can be applied noninvasively, repeatedly, and at low additional cost.

Status

SIGNED

Call topic

ERC-2019-COG

Update Date

27-04-2024
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Horizon 2020
H2020-EU.1. EXCELLENT SCIENCE
H2020-EU.1.1. EXCELLENT SCIENCE - European Research Council (ERC)
ERC-2019
ERC-2019-COG