Radiomics to predict immunotherapy-induced pneumonitis: proof of concept

Rivka R. Colen, Takeo Fujii, Mehmet Asim Bilen, Aikaterini Kotrotsou, Srishti Abrol, Kenneth R. Hess, Joud Hajjar, Maria E. Suarez-Almazor, Anas Alshawa, David S. Hong, Dunia Giniebra-Camejo, Bettzy Stephen, Vivek Subbiah, Ajay Sheshadri, Tito Mendoza, Siqing Fu, Padmanee Sharma, Funda Meric-Bernstam, Aung Naing

Research output: Contribution to journalArticlepeer-review

85 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)601-607
Number of pages7
JournalInvestigational New Drugs
Volume36
Issue number4
DOIs
StatePublished - Aug 1 2018

Keywords

  • Immune-related adverse event
  • Immunotherapy
  • Pneumonitis
  • Radiomics

ASJC Scopus subject areas

  • Oncology
  • Pharmacology
  • Pharmacology (medical)

MD Anderson CCSG core facilities

  • Biostatistics Resource Group

Fingerprint

Dive into the research topics of 'Radiomics to predict immunotherapy-induced pneumonitis: proof of concept'. Together they form a unique fingerprint.

Cite this