AI Article Synopsis

  • The study categorized pancreatic ductal adenocarcinoma (PDAC) using imaging techniques based on qualitative (high or low delta) assessments of tumors observed in CT scans.
  • A new quantitative classification method (q-delta) was developed, showing that low q-delta tumors consistently correlate with better patient outcomes and survival rates compared to high q-delta tumors.
  • The findings indicate that this q-delta classification could serve as a valuable tool in clinical settings and may enhance the design of future clinical trials for PDAC.

Article Abstract

Previously, we characterized qualitative imaging-based subtypes of pancreatic ductal adenocarcinoma (PDAC) on computed tomography (CT) scans. Conspicuous (high delta) PDAC tumors are more likely to have aggressive biology and poorer clinical outcomes compared to inconspicuous (low delta) tumors. Here, we developed a quantitative classification of this imaging-based subtype (quantitative delta; q-delta). Retrospectively, baseline pancreatic protocol CT scans of three cohorts (cohort#1 = 101, cohort#2 = 90 and cohort#3 = 16 [external validation]) of patients with PDAC were qualitatively classified into high and low delta. We used a voxel-based method to volumetrically quantify tumor enhancement while referencing normal-pancreatic-parenchyma and used machine learning-based analysis to build a predictive model. In addition, we quantified the stromal content using hematoxylin- and eosin-stained treatment-naïve PDAC sections. Analyses revealed that PDAC quantitative enhancement values are predictive of the qualitative delta scoring and were used to build a classification model (q-delta). Compared to high q-delta, low q-delta tumors were associated with improved outcomes, and the q-delta class was an independent prognostic factor for survival. In addition, low q-delta tumors had higher stromal content and lower cellularity compared to high q-delta tumors. Our results suggest that q-delta classification provides a clinically and biologically relevant tool that may be integrated into ongoing and future clinical trials.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762105PMC
http://dx.doi.org/10.3390/cancers12123656DOI Listing

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