Frontiers in Oncology (May 2022)

Pre-Treatment Computed Tomography Radiomics for Predicting the Response to Neoadjuvant Chemoradiation in Locally Advanced Rectal Cancer: A Retrospective Study

  • Yitao Mao,
  • Yitao Mao,
  • Qian Pei,
  • Yan Fu,
  • Yan Fu,
  • Haipeng Liu,
  • Changyong Chen,
  • Haiping Li,
  • Guanghui Gong,
  • Hongling Yin,
  • Peipei Pang,
  • Huashan Lin,
  • Biaoxiang Xu,
  • Hongyan Zai,
  • Xiaoping Yi,
  • Xiaoping Yi,
  • Xiaoping Yi,
  • Xiaoping Yi,
  • Bihong T. Chen

DOI
https://doi.org/10.3389/fonc.2022.850774
Journal volume & issue
Vol. 12

Abstract

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Background and PurposeComputerized tomography (CT) scans are commonly performed to assist in diagnosis and treatment of locally advanced rectal cancer (LARC). This study assessed the usefulness of pretreatment CT-based radiomics for predicting pathological complete response (pCR) of LARC to neoadjuvant chemoradiotherapy (nCRT).Materials and MethodsPatients with LARC who underwent nCRT followed by total mesorectal excision surgery from July 2010 to December 2018 were enrolled in this retrospective study. A total of 340 radiomic features were extracted from pretreatment contrast-enhanced CT images. The most relevant features to pCR were selected using the least absolute shrinkage and selection operator (LASSO) method and a radiomic signature was generated. Predictive models were built with radiomic features and clinico-pathological variables. Model performance was assessed with decision curve analysis and was validated in an independent cohort.ResultsThe pCR was achieved in 44 of the 216 consecutive patients (20.4%) in this study. The model with the best performance used both radiomics and clinical variables including radiomic signatures, distance to anal verge, lymphocyte-to-monocyte ratio, and carcinoembryonic antigen. This combined model discriminated between patients with and without pCR with an area under the curve of 0.926 and 0.872 in the training and the validation cohorts, respectively. The combined model also showed better performance than models built with radiomic or clinical variables alone.ConclusionOur combined predictive model was robust in differentiating patients with and without response to nCRT.

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