4.5 Article

Radiomics to predict immunotherapy-induced pneumonitis: proof of concept

期刊

INVESTIGATIONAL NEW DRUGS
卷 36, 期 4, 页码 601-607

出版社

SPRINGER
DOI: 10.1007/s10637-017-0524-2

关键词

Immunotherapy; Immune-related adverse event; Pneumonitis; Radiomics

资金

  1. John S. Dunn Sr. Distinguished Chair in Diagnostic Imaging Fund
  2. University of Texas MD Anderson Brain Tumor Center Program
  3. University of Texas MD Anderson Cancer Center startup funding
  4. Cancer Prevention and Research Institute of Texas Individual Investigator Research Award [RP160150]
  5. University of Texas MD Anderson Cancer Center support grant [P30 CA016672]
  6. K23 Career Development Award from the National Institutes of Health [K23AI117024]

向作者/读者索取更多资源

We present the first reported work that explores the potential of radiomics to predict patients who are at risk for developing immunotherapy-induced pneumonitis. Despite promising results with immunotherapies, immune-related adverse events (irAEs) are challenging. Although less common, pneumonitis is a potentially fatal irAE. Thus, early detection is critical for improving treatment outcomes; an urgent need to identify biomarkers that predict patients at risk for pneumonitis exists. Radiomics, an emerging field, is the automated extraction of high fidelity, high-dimensional imaging features from standard medical images and allows for comprehensive visualization and characterization of the tissue of interest and corresponding microenvironment. In this pilot study, we sought to determine whether radiomics has the potential to predict development of pneumonitis. We performed radiomic analyses using baseline chest computed tomography images of patients who did (N = 2) and did not (N = 30) develop immunotherapy-induced pneumonitis. We extracted 1860 radiomic features in each patient. Maximum relevance and minimum redundancy feature selection method, anomaly detection algorithm, and leave-one-out cross-validation identified radiomic features that were significantly different and predicted subsequent immunotherapy-induced pneumonitis (accuracy, 100% [p = 0.0033]). This study suggests that radiomic features can classify and predict those patients at baseline who will subsequently develop immunotherapy-induced pneumonitis, further enabling risk-stratification that will ultimately lead to better treatment outcomes.

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