Whole-lesion apparent diffusion coefficient (ADC) histogram as a quantitative biomarker to preoperatively differentiate stage IA endometrial carcinoma from benign endometrial lesions

Abstract Background To assess the value of whole-lesion apparent diffusion coefficient (ADC) histogram analysis in differentiating stage IA endometrial carcinoma (EC) from benign endometrial lesions (BELs) and characterizing histopathologic features of stage IA EC preoperatively. Methods One hundred...

Full description

Bibliographic Details
Main Authors: Jieying Zhang, Xiaoduo Yu, Xiaomiao Zhang, Shuang Chen, Yan Song, Lizhi Xie, Yan Chen, Han Ouyang
Format: Article
Language:English
Published: BMC 2022-08-01
Series:BMC Medical Imaging
Subjects:
Online Access:https://doi.org/10.1186/s12880-022-00864-9
_version_ 1828300279730143232
author Jieying Zhang
Xiaoduo Yu
Xiaomiao Zhang
Shuang Chen
Yan Song
Lizhi Xie
Yan Chen
Han Ouyang
author_facet Jieying Zhang
Xiaoduo Yu
Xiaomiao Zhang
Shuang Chen
Yan Song
Lizhi Xie
Yan Chen
Han Ouyang
author_sort Jieying Zhang
collection DOAJ
description Abstract Background To assess the value of whole-lesion apparent diffusion coefficient (ADC) histogram analysis in differentiating stage IA endometrial carcinoma (EC) from benign endometrial lesions (BELs) and characterizing histopathologic features of stage IA EC preoperatively. Methods One hundred and six BEL and 126 stage IA EC patients were retrospectively enrolled. Eighteen volumetric histogram parameters were extracted from the ADC map of each lesion. The Mann–Whitney U or Student’s t-test was used to compare the differences between the two groups. Models based on clinical parameters and histogram features were established using multivariate logistic regression. Receiver operating characteristic (ROC) analysis and calibration curves were used to assess the models. Results Stage IA EC showed lower ADC10th, ADC90th, ADCmin, ADCmax, ADCmean, ADCmedian, interquartile range, mean absolute deviation, robust mean absolute deviation (rMAD), root mean squared, energy, total energy, entropy, variance, and higher skewness, kurtosis and uniformity than BELs (all p < 0.05). ADCmedian yielded the highest area under the ROC curve (AUC) of 0.928 (95% confidence interval [CI] 0.895–0.960; cut-off value = 1.161 × 10−3 mm2/s) for differentiating stage IA EC from BELs. Moreover, multivariate analysis demonstrated that ADC-score (ADC10th + skewness + rMAD + total energy) was the only significant independent predictor (OR = 2.641, 95% CI 2.045–3.411; p < 0.001) for stage IA EC when considering clinical parameters. This ADC histogram model (ADC-score) achieved an AUC of 0.941 and a bias-corrected AUC of 0.937 after bootstrap resampling. The model performed well for both premenopausal (accuracy = 0.871) and postmenopausal (accuracy = 0.905) patients. Besides, ADCmin and ADC10th were significantly lower in Grade 3 than in Grade 1/2 stage IA EC (p = 0.022 and 0.047). At the same time, no correlation was found between ADC histogram parameters and the expression of Ki-67 in stage IA EC (all p > 0.05). Conclusions Whole-lesion ADC histogram analysis could serve as an imaging biomarker for differentiating stage IA EC from BELs and assisting in tumor grading of stage IA EC, thus facilitating personalized clinical management for premenopausal and postmenopausal patients.
first_indexed 2024-04-13T13:07:00Z
format Article
id doaj.art-0898f1eb5bd7456b8d353b72df9b50f0
institution Directory Open Access Journal
issn 1471-2342
language English
last_indexed 2024-04-13T13:07:00Z
publishDate 2022-08-01
publisher BMC
record_format Article
series BMC Medical Imaging
spelling doaj.art-0898f1eb5bd7456b8d353b72df9b50f02022-12-22T02:45:44ZengBMCBMC Medical Imaging1471-23422022-08-0122111410.1186/s12880-022-00864-9Whole-lesion apparent diffusion coefficient (ADC) histogram as a quantitative biomarker to preoperatively differentiate stage IA endometrial carcinoma from benign endometrial lesionsJieying Zhang0Xiaoduo Yu1Xiaomiao Zhang2Shuang Chen3Yan Song4Lizhi Xie5Yan Chen6Han Ouyang7Department of Diagnostic Radiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeDepartment of Diagnostic Radiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeDepartment of Diagnostic Radiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeDepartment of Diagnostic Radiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeDepartment of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeMR Research China, GE HealthcareDepartment of Diagnostic Radiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeDepartment of Diagnostic Radiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeAbstract Background To assess the value of whole-lesion apparent diffusion coefficient (ADC) histogram analysis in differentiating stage IA endometrial carcinoma (EC) from benign endometrial lesions (BELs) and characterizing histopathologic features of stage IA EC preoperatively. Methods One hundred and six BEL and 126 stage IA EC patients were retrospectively enrolled. Eighteen volumetric histogram parameters were extracted from the ADC map of each lesion. The Mann–Whitney U or Student’s t-test was used to compare the differences between the two groups. Models based on clinical parameters and histogram features were established using multivariate logistic regression. Receiver operating characteristic (ROC) analysis and calibration curves were used to assess the models. Results Stage IA EC showed lower ADC10th, ADC90th, ADCmin, ADCmax, ADCmean, ADCmedian, interquartile range, mean absolute deviation, robust mean absolute deviation (rMAD), root mean squared, energy, total energy, entropy, variance, and higher skewness, kurtosis and uniformity than BELs (all p < 0.05). ADCmedian yielded the highest area under the ROC curve (AUC) of 0.928 (95% confidence interval [CI] 0.895–0.960; cut-off value = 1.161 × 10−3 mm2/s) for differentiating stage IA EC from BELs. Moreover, multivariate analysis demonstrated that ADC-score (ADC10th + skewness + rMAD + total energy) was the only significant independent predictor (OR = 2.641, 95% CI 2.045–3.411; p < 0.001) for stage IA EC when considering clinical parameters. This ADC histogram model (ADC-score) achieved an AUC of 0.941 and a bias-corrected AUC of 0.937 after bootstrap resampling. The model performed well for both premenopausal (accuracy = 0.871) and postmenopausal (accuracy = 0.905) patients. Besides, ADCmin and ADC10th were significantly lower in Grade 3 than in Grade 1/2 stage IA EC (p = 0.022 and 0.047). At the same time, no correlation was found between ADC histogram parameters and the expression of Ki-67 in stage IA EC (all p > 0.05). Conclusions Whole-lesion ADC histogram analysis could serve as an imaging biomarker for differentiating stage IA EC from BELs and assisting in tumor grading of stage IA EC, thus facilitating personalized clinical management for premenopausal and postmenopausal patients.https://doi.org/10.1186/s12880-022-00864-9Endometrial neoplasmsApparent diffusion coefficientDiffusion-weighted MRIHistogram analysis
spellingShingle Jieying Zhang
Xiaoduo Yu
Xiaomiao Zhang
Shuang Chen
Yan Song
Lizhi Xie
Yan Chen
Han Ouyang
Whole-lesion apparent diffusion coefficient (ADC) histogram as a quantitative biomarker to preoperatively differentiate stage IA endometrial carcinoma from benign endometrial lesions
BMC Medical Imaging
Endometrial neoplasms
Apparent diffusion coefficient
Diffusion-weighted MRI
Histogram analysis
title Whole-lesion apparent diffusion coefficient (ADC) histogram as a quantitative biomarker to preoperatively differentiate stage IA endometrial carcinoma from benign endometrial lesions
title_full Whole-lesion apparent diffusion coefficient (ADC) histogram as a quantitative biomarker to preoperatively differentiate stage IA endometrial carcinoma from benign endometrial lesions
title_fullStr Whole-lesion apparent diffusion coefficient (ADC) histogram as a quantitative biomarker to preoperatively differentiate stage IA endometrial carcinoma from benign endometrial lesions
title_full_unstemmed Whole-lesion apparent diffusion coefficient (ADC) histogram as a quantitative biomarker to preoperatively differentiate stage IA endometrial carcinoma from benign endometrial lesions
title_short Whole-lesion apparent diffusion coefficient (ADC) histogram as a quantitative biomarker to preoperatively differentiate stage IA endometrial carcinoma from benign endometrial lesions
title_sort whole lesion apparent diffusion coefficient adc histogram as a quantitative biomarker to preoperatively differentiate stage ia endometrial carcinoma from benign endometrial lesions
topic Endometrial neoplasms
Apparent diffusion coefficient
Diffusion-weighted MRI
Histogram analysis
url https://doi.org/10.1186/s12880-022-00864-9
work_keys_str_mv AT jieyingzhang wholelesionapparentdiffusioncoefficientadchistogramasaquantitativebiomarkertopreoperativelydifferentiatestageiaendometrialcarcinomafrombenignendometriallesions
AT xiaoduoyu wholelesionapparentdiffusioncoefficientadchistogramasaquantitativebiomarkertopreoperativelydifferentiatestageiaendometrialcarcinomafrombenignendometriallesions
AT xiaomiaozhang wholelesionapparentdiffusioncoefficientadchistogramasaquantitativebiomarkertopreoperativelydifferentiatestageiaendometrialcarcinomafrombenignendometriallesions
AT shuangchen wholelesionapparentdiffusioncoefficientadchistogramasaquantitativebiomarkertopreoperativelydifferentiatestageiaendometrialcarcinomafrombenignendometriallesions
AT yansong wholelesionapparentdiffusioncoefficientadchistogramasaquantitativebiomarkertopreoperativelydifferentiatestageiaendometrialcarcinomafrombenignendometriallesions
AT lizhixie wholelesionapparentdiffusioncoefficientadchistogramasaquantitativebiomarkertopreoperativelydifferentiatestageiaendometrialcarcinomafrombenignendometriallesions
AT yanchen wholelesionapparentdiffusioncoefficientadchistogramasaquantitativebiomarkertopreoperativelydifferentiatestageiaendometrialcarcinomafrombenignendometriallesions
AT hanouyang wholelesionapparentdiffusioncoefficientadchistogramasaquantitativebiomarkertopreoperativelydifferentiatestageiaendometrialcarcinomafrombenignendometriallesions