Abstract

The aim of this study was to create a radiomics model for Locally Advanced Cervical Cancer (LACC) patients to predict pathological complete response (pCR) after neoadjuvant chemoradiotherapy (NACRT) analysing T2-weighted 1.5 T magnetic resonance imaging (MRI) acquired before treatment start. Patients with LACC and an International Federation of Gynecology and Obstetrics stage from IB2 to IVA at diagnosis were retrospectively enrolled for this study. All patients underwent NACRT, followed by radical surgery; pCR―assessed on surgical specimen―was defined as absence of any residual tumour. Finally, 1889 features were extracted from MR images; features showing statistical significance in predicting pCR at the univariate analysis were selected following an iterative method, which was ad-hoc developed for this study. Based on this method, 15 different classifiers were trained considering the most significant features selected. Model selection was carried out using the area under the receiver operating characteristic curve (AUC) as target metrics. One hundred eighty-three patients from two institutions were analysed. The model, showing the highest performance with an AUC of 0.80, was the random forest method initialised with default parameters. Radiomics appeared to be a reliable tool in pCR prediction for LACC patients undergoing NACRT, supporting the identification of patient risk groups, which paves treatment pathways tailored according to the predicted outcome.

Highlights

  • IntroductionCervical cancer (CC) represents the fourth leading cause of cancer death in women, with 311,000 deaths in 2018 worldwide [1]

  • The aim of this study was to investigate the potential role of magnetic resonance imaging (MRI) radiomics, used for staging, to predict pathological complete response (pCR) following neoadjuvant chemoradiotherapy (NACRT) in Locally Advanced Cervical Cancer (LACC) patients with different Federation of Gynecology and Obstetrics (FIGO) stages

  • Patients affected by LACC, with FIGO stage from IB2 to IVA, treated in two different institutions, were considered for this retrospective analysis

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Summary

Introduction

Cervical cancer (CC) represents the fourth leading cause of cancer death in women, with 311,000 deaths in 2018 worldwide [1]. Treatment depends mainly on the stage of the tumour at diagnosis, as assessed by the International Federation of Gynecology and Obstetrics (FIGO) 2009 staging system [2]. Advanced stages are usually treated with external beam radiotherapy in association with platinum-based chemotherapy (CRT) followed by brachytherapy boost [3]. Survival rates for women with Locally Advanced Cervical Cancer (LACC) are improving, one in three women develop local and pelvic recurrences, which supports the hypothesis of residual disease presence after definitive chemoradiation therapy [4]

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