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External validation and comparison of MR-based radiomics models for predicting pathological complete response in locally advanced rectal cancer: a two-centre, multi-vendor study

  • Imaging Informatics and Artificial Intelligence
  • Published:
European Radiology Aims and scope Submit manuscript

Abstract

Objectives

The aim of this study was two-fold: (1) to develop and externally validate a multiparameter MR-based machine learning model to predict the pathological complete response (pCR) in locally advanced rectal cancer (LARC) patients after neoadjuvant chemoradiotherapy (nCRT), and (2) to compare different classifiers’ discriminative performance for pCR prediction.

Methods

This retrospective study includes 151 LARC patients divided into internal (centre A, n = 100) and external validation set (centre B, n = 51). The clinical and MR radiomics features were derived to construct clinical, radiomics, and clinical-radiomics model. Random forest (RF), support vector machine (SVM), logistic regression (LR), K-nearest neighbor (KNN), naive Bayes (NB), and extreme gradient boosting (XGBoost) were used as classifiers. The predictive performance was assessed using the receiver operating characteristic (ROC) curve.

Results

Eleven radiomics and four clinical features were chosen as pCR-related signatures. In the radiomics model, the RF algorithm achieved 74.0% accuracy (an AUC of 0.863) and 84.4% (an AUC of 0.829) in the internal and external validation sets. In the clinical-radiomics model, RF algorithm exhibited high and stable predictive performance in the internal and external validation datasets with an AUC of 0.906 (87.3% sensitivity, 73.7% specificity, 76.0% accuracy) and 0.872 (77.3% sensitivity, 88.2% specificity, 86.3% accuracy), respectively. RF showed a better predictive performance than the other classifiers in the external validation datasets of three models.

Conclusions

The multiparametric clinical-radiomics model combined with RF algorithm is optimal for predicting pCR in the internal and external sets, and might help improve clinical stratifying management of LARC patients.

Key Points

A two-centre study showed that radiomics analysis of pre- and post-nCRT multiparameter MR images could predict pCR in patients with LARC.

The combined model was superior to the clinical and radiomics model in predicting pCR in locally advanced rectal cancer.

The RF classifier performed best in the current study.

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Abbreviations

AUC:

Area under the ROC curve

CEA:

Carcinoembryonic antigen

DL:

Deep learning

DWI:

Diffusion-weighted imaging

KNN:

K-nearest neighbor

LARC:

Locally advanced rectal cancer

LASSO:

Least absolute shrinkage and selection operator

LoG:

Laplacian of Gaussian

LR:

Logistic regression

ML:

Machine learning

NB:

Naive Bayes

nCRT:

Neoadjuvant chemoradiotherapy

pCR:

Pathologic complete response

pN:

Pathologic N stage

pT:

Pathologic N stage

RF:

Random forest

SVM:

Support vector machine

T2WI:

T2-weighted imaging

TME:

Total mesorectal excision

TRG:

Tumour regression grade

VOI:

Volume of interest

XGBoost:

Extreme gradient boosting

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Funding

This study has received funding from the Youth Talent Project of The Second Affiliated Hospital of Guangzhou University of Chinese Medicine (Grant Number ZY2022YL05).

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Correspondence to Wei Yang or Xian Liu.

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Guarantor

The scientific guarantor of this publication is Xian Liu Ph.D., M.D., and Wei Yang Ph.D., M.D.

Conflict of interest

One of the authors (Kan Deng) is an employee of Philips Healthineers. The remaining authors declare no relationships with any companies whose products or services may be related to the subject matter of the article.

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No complex statistical methods were necessary for this paper.

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Written informed consent was not required for this study because of the retrospective nature of the study.

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Institutional review board approval was obtained.

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• retrospective

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• performed at two institutions

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Wei, Q., Chen, Z., Tang, Y. et al. External validation and comparison of MR-based radiomics models for predicting pathological complete response in locally advanced rectal cancer: a two-centre, multi-vendor study. Eur Radiol 33, 1906–1917 (2023). https://doi.org/10.1007/s00330-022-09204-5

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