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Radial Data Mining to Identify Density-Dose Interactions That Predict Distant Failure Following SABR.
Angela Davey1, Marcel van Herk1,2, Corinne Faivre-Finn1,2,3
1Division of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, United Kingdom.
Frontiers in Oncology
|March 31, 2022
Summary
Lower doses outside the gross tumor volume (GTV) increase distant metastasis risk. Tumor density interacts with incidental dose, indicating imaging can guide dose escalation for lung cancer patients.
Area of Science:
- Radiation Oncology
- Medical Imaging
- Data Mining
Background:
- Lower incidental doses in lung stereotactic radiotherapy correlate with increased distant metastasis (DM).
- Pretreatment computed tomography (CT) tumor density is linked to microscopic disease (MDE) risk.
- The interaction between imaging biomarkers and incidental dose remains unexplored.
Purpose of the Study:
- To investigate density-dose interactions radially from the gross tumor volume (GTV) to predict DM.
- To determine if imaging can inform dose escalation decisions for patients at risk.
- To explore the impact of incidental dose on outcome based on tumor imaging characteristics.
Main Methods:
- Quantified dose and density in 1-mm annuli around the GTV for 199 lung cancer patients.
- Utilized Cox regressions with dose-density interactions in independent annuli.
- Created heatmaps to visualize DM prediction improvement due to interactions.
Main Results:
- Dose-density interactions significantly improved DM prediction in over 50% of bootstrap resamples.
- Tumor density variance and high peritumour density were associated with DM in patients with specific dose distributions outside the GTV.
- Identified dose-density associations were independent of the mean GTV dose.
Conclusions:
- High tumor variance and peritumour density increase DM risk with low/non-uniform incidental doses outside the GTV.
- Incidental dose plays a crucial role in controlling occult disease, independent of tumor dose.
- This methodology enables spatial dose-density interaction studies, potentially accelerating clinical implementation of imaging biomarkers.
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